The Effects of Sprint Interval Training on Physical Performance: A Systematic Review and Meta-Analysis : The Journal of Strength & Conditioning Research

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The Effects of Sprint Interval Training on Physical Performance: A Systematic Review and Meta-Analysis

Hall, Andy J.1; Aspe, Rodrigo R.1; Craig, Thomas P.1; Kavaliauskas, Mykolas2; Babraj, John3; Swinton, Paul A.1

Author Information
Journal of Strength and Conditioning Research 37(2):p 457-481, February 2023. | DOI: 10.1519/JSC.0000000000004257

Abstract

Introduction

Interval training is considered a time efficient approach to exercise that can produce physical performance benefits (83) that are at least equivalent to those obtained with traditional endurance training (42,68). Interval training involves repeated bouts of intense exercise interspersed with recovery periods of low-intensity activity or rest (8). Two of the most frequently investigated forms of interval training include high-intensity interval training (HIIT) and sprint interval training (SIT). High-intensity interval training has been defined as repeated short-to-long bouts of exercise performed at a power output or velocity within the severe-intensity domain between the second ventilatory threshold and maximal oxygen consumption (V̇o2max) (86). Therefore, HIIT requires “near maximal” efforts that elicit an intensity of ≥80% of maximal heart rate (HRmax) or V̇o2max (108). Also, it is frequently performed using a range of exercise modes, including running (31), cycling (99), rowing (1), and swimming (97); resulting in wide applicability to trained and untrained populations. In contrast, SIT is defined by exercise performed at a power output or velocity above V̇o2max (i.e., “all-out” efforts in the extreme-intensity domain) necessitating short bouts of exercise (86). Within research studies, SIT is most often performed on a cycle ergometer, allowing a controlled application of training intensity through the application of substantive resistance over 6- to 30-second intervals (2,62,111). The potential for SIT to generate large physiological improvements in a time efficient manner has resulted in uptake by athletes, thus becoming its own stand-alone training modality, where research findings have identified improvements in performance measures of competitive runners (53), cyclists (69), triathletes (33), and ice hockey players (74).

Although previous research has demonstrated that there may be overlap between adaptations produced from both HIIT and SIT (77), differences are likely to exist for a selection of both aerobic and anaerobic outcomes, and delineation between the 2 training methods is important for future understanding. Additionally, Viana et al. (107) identified the importance of careful evaluation of acute program variables when comparing findings from studies either within or across forms of interval training. Creation of an interval training session is complex and first involves the manipulation of several interconnected acute program variables, including interval intensity, work interval duration, recovery intensity, recovery duration, exercise modality, number of repetitions, number of series, series duration, time between series, and between series recovery intensity (14). Individual sessions can then be altered within a training microcycle and progressed over longer periods to create overload and continued adaptations. However, current knowledge regarding the effects of acute program variables and their interaction is in the early stages, particularly with regards to SIT and the range of different outcomes that may be of interest to athletes.

Previous systematic reviews and meta-analyses have attempted to synthesize an increasing evidence base focusing on SIT performed on a cycle ergometer and its effects on aerobic capacity (44,86,94,109,110) and sprint power (110). These evidence synthesis studies have generally included data from healthy individuals between 18 and 45 years, who were either sedentary or engaged in moderate frequency recreational activities (44,86,94,109,110). Additionally, previous evidence synthesis studies have chosen to focus on a restricted range of outcome variables and SIT protocols. Rosenblat et al. (86) meta-analyzed results from studies directly comparing HIIT and SIT interventions with time-to-exhaustion tests. The analysis was restricted to 6 studies that met the inclusion criteria, with the primary analysis identifying no differences between the forms of interval training. Sloth et al. (94) and Gist et al. (44) both investigated the effectiveness of SIT interventions to improve V̇o2max. Gist et al. (44) restricted their analysis to SIT interventions employing the popular repeated Wingate protocol comprising 4–6 “all-out” 30-second sprints with approximately 4 minutes of recovery. The meta-analysis included 16 studies and compared SIT interventions with either traditional endurance training or no-exercise controls. When analyzed separately, the results demonstrated a moderate effect (d = 0.69 [95% CI: 0.46–0.93]) of SIT compared with no-exercise controls, and no effect (d = 0.04 [95% CI: −0.17 to 0.24]) of SIT when compared with traditional endurance training. Similar findings were obtained in the meta-analysis conducted by Sloth et al. (94), which included 21 studies with a wider range of SIT protocols (10- to 30-s sprints) incorporating either noncontrolled or no-exercise-controlled designs. Sloth et al. (94) also reported a moderate effect (d = 0.63 [95% CI: 0.39–0.87]) of SIT to improve V̇o2max. In contrast, Weston et al. (110) acknowledged that SIT performed on a cycle ergometer had the potential to improve sprint performance and aerobic capacity. The authors' meta-analyzed results from 16 studies, including either controlled or noncontrolled designs that measured power produced during a maximum 30-second sprint. The analysis was restricted to SIT studies employing the repeated Wingate protocol, with results demonstrating that SIT interventions had an unclear effect on improvements in peak (+1.8% [90% CL: ±5.0]) and mean (+2.2% [90% CL: ±10.3]) power.

Given the work of previous meta-analyses, Vollaard et al. (109) stated that it was surprising that there had been minimal attempt to identify “optimal” protocols. As a result, the authors investigated the modifying effects of maximum number of sprints, intervention duration, number of sessions, sprint duration, recovery time, and sprint resistance on V̇o2max in 34 studies. The results indicated a possible small modifying effect of the maximum number of sprints, with decreased improvements with additional sprints (109). All other program variables were found to exert unclear or trivial effects (109). However, the meta-analysis conducted by Vollaard et al. (109) included a limited number of data points and only focused on a single outcome variable. The inclusion of a limited number of outcome measures in previous meta-analyses is no longer reflective of the research area with studies investigating a range of outcomes including those that assess anaerobic (113), neural (26), and force production systems (106).

Given the recent increase in the number of diverse SIT protocols to improve a range of fitness parameters associated with physical performance and sporting activity, there is a need to synthesize the available evidence and identify the protocols that are most effective. This would provide athletes, practitioners, and researchers with a practical framework for SIT prescriptions targeting specific training outcomes. Therefore, the aim of this systematic review and meta-analysis was to perform a comprehensive synthesis of the published research and quantify the effect of SIT and potential moderators on a range of physical performance measures collected from healthy adults. Additionally, assessment of the overall research quality was made to combine with the meta-analytic findings to better inform current practice and future research.

Methods

Search Strategy

This review was performed in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement (70). A 3-step search strategy was employed; first, an initial limited search was performed in MEDLINE and SportDiscuss followed by an analysis of the text words contained in the resulting titles, abstracts, keywords, and index terms used to describe the publications. Second, a search strategy tailored to each information source (MEDLINE, Web of Science, SPORTDiscuss) was developed based on the identified keywords and index terms (e.g., “sprint interval training,” “high intensity interval training,” “high intensity intermittent training,” “HIIT,” “interval exercise,” “high intensity training,” “high intensity exercise,” “high intensity aerobic interval training,” and “aerobic interval training”) and executed. Finally, the reference lists of all included studies as well as forward citation tracking using Google Scholar were searched for additional sources. Searches were limited to the years 2000–February 2020 and to the English language. The full electronic search strategy, including limits, can be found in Electronic Supplementary Material (see Appendix S1, https://links.lww.com/JSCR/A325).

Inclusion Criteria

Studies were included in this review if they satisfied the population, intervention, comparator, outcome (PICO) criteria—Population: young to middle-aged adults (mean age, 18–45 years), not suffering from any acute or chronic disease. Studies that specifically recruited overweight or obese subjects were excluded. Intervention: a minimum of 2 weeks of duration comprising maximum-intensity (“all-out”) sprints on a resistance bike. Interventions comprising sprints greater than 30-second duration were not considered maximum intensity and therefore were excluded. Studies incorporating combined training interventions (e.g., SIT plus strength training or aerobic training) or combined supplement interventions (e.g., SIT plus creatine supplementation) were excluded. Comparator: cohort, nonrandomized, and randomized-controlled (no exercise or habitual physical activity) designs. Where studies compared relevant SIT groups with other modes of exercise, data from SIT groups were included. Outcome: Three-outcome categories were defined and included: (a) aerobic (e.g., V̇o2max, incremental time, oxygen consumption [O2], respiratory exchange ration [RER]), (b) anaerobic (e.g., Wingate peak power, Wingate mean power), and (c) mixed aerobic-anaerobic (e.g., total work across critical power test measures, peak power across repeated tests).

Study Selection

Search results were imported to Proquest Refworks and duplicates were removed. Titles and abstracts of all sources were screened by 2 independent reviewers (A.J.H. and T.P.C.) for relevance to the review questions. Full-text manuscripts were retrieved for articles that potentially met the inclusion criteria and were screened independently by the same 2 reviewers. At each stage of the screening process, disagreements were resolved by discussion and inclusion of a third reviewer (P.A.S.). Articles identified from hand searching of reference lists were assessed for relevance based on their titles and abstracts with those meeting inclusion criteria added to the full-text screening stage. Full-text studies that did not meet the inclusion criteria were excluded, and reasons for their exclusion were documented (See Appendix S2, Electronic Supplementary Material, https://links.lww.com/JSCR/A325).

Data Extraction

A bespoke data extraction tool was piloted on 10 studies by 2 independent reviewers and discussed within the research team before full data extraction. Data extraction was completed independently by 2 authors (A.J.H. and T.P.C.) and discrepancies resolved through discussion. Reviewers were not blinded to manuscript authors or journals. Data regarding study type (controlled, uncontrolled), subject characteristics (sex, age, body mass, number), training parameters (intervention duration, total number of training sessions, exercise bike used, number of sprint repetitions within training intervention, sprint duration, recovery duration, applied sprint resistance), and training outcome measures were extracted. All extracted outcome data were assigned to a single-outcome category. Where data were presented in figures or percentage change units, the corresponding author was contacted for the original information. Where this was not made available, data within figures were extracted through graph digitizer software (DigitizeIt, Germany), with data expressed in percentage change units omitted from extraction.

Evaluation of Methodological Quality

Methodological quality and risk of bias were evaluated by 3 independent reviewers (T.P.C., R.R.A., M.K.) with agreement reached on each item by at least 2 reviewers. The quality of each review outcome category was assigned using a strategy based on the recommendations of the Grading of Recommendations Assessment Development and Evaluation (GRADE) working group (45). Each individual study was initially appraised using a modified version of the Downs and Black Checklist (28), which was specifically tailored for use in this study (See Appendix S3, Electronic Supplementary Material, https://links.lww.com/JSCR/A325). The modified checklist comprised 23 outcomes for comparator studies and 19 outcomes for noncomparator studies after removal of items relating to group differences. A total of 4 domains were evaluated, including (a) reporting, (b) internal validity—bias, (c) internal validity—confounding, and (d) statistical power. A total of 5 items were added to both checklists and included the following: “Were familiarization sessions of training completed?” “Were familiarization sessions of testing completed?” (internal validity—bias); “Were number of sessions attended reported?” “Was a minimum number of sessions for inclusion reported” (reporting); and “If a power calculation was completed, was this adjusted to account for multiple outcome variables?” (statistical power). Scoring for the additional questions employed the same protocol for the original questions: Yes = 1, No = 0, Unable to determine = 0. These additional items were included because they were considered fundamental in determining precision of the effects of an intervention and associated statistical rigor. Individual studies were assigned a rating based on the percentage of items scored positively with the following criteria used: “high” (80% +), “moderate” (60–79%), “low” (40–59%), or “very low” (0–39%). For each of the primary meta-analysis outcomes, an overall quality rating was assigned based on the mode rating of individual studies contributing data.

Statistical Analyses

A Bayesian’s framework was chosen over frequentist methods to provide a more flexible modeling approach and enable results to be interpreted intuitively through reporting of subjective probabilities (55). The effects of SIT on included outcomes were quantified by calculating effect sizes in the form of standardized mean differences (SMDs). Magnitude-based SMDs obtained by dividing the mean difference by the preintervention standard deviation are the most popular form of effect size used in meta-analyses in sport and exercise science and are informative when considering the change an individual can be expected to make relative to a population pre- to postintervention (21). Most studies did not include a no-exercise control, and so intervention group–only effect sizes were used for primary analyses. Sensitivity analyses were conducted where possible with effect sizes incorporating data from no-exercise controls (72). Within-study variance of effect sizes were calculated according to standard distributions with bias correction for small samples applied to both the effect size estimate and its variance (21). Standardized mean difference effect sizes are equal to Dz effect sizes calculated using a pre-post correlation of 0.5. Dz effect sizes account for the pre-post correlation, and generally result in larger effect sizes than SMD effect sizes, since the pre-post correlations are typically larger than 0.5. Dz effect sizes can be calculated using the SD of the difference scores or mathematically accounting for the pre-post correlation, if the correlation is reported. However, such distributions are influenced by pre-post correlations that are generally not reported (87). Therefore, within-study variances were calculated and inputted using a standard value of 0.7 (32), with an additional error term included to enable individual study values to vary. An informative Gaussian prior was placed on the error term such that the overall distribution of values matched the within-study variance distribution obtained from correlation values ranging from approximately 0.5 to 0.9 (32). Three-level random-effects Bayesian’s hierarchical models were used to pool effect sizes and model average effects, variance between studies, and covariance of multiple outcomes reported in the same study (e.g., reporting of a single outcome across multiple time points or reporting values from multiple outcomes). The overall analysis approach was determined a priori and included an initial pooling of all effect sizes, followed by investigation of average effects by outcome category and training status. Meta-regressions were then performed to investigate associations between effect sizes and intervention duration, training intensity, training volume, and training work-to-rest ratios. Meta-regressions were only performed where there were sufficient data including a minimum of 4 data points per category level or 10 data points for continuous variables (37).

Noninformative priors were used for all model parameters other than the within study variance correlations. Inferences from all analyses were performed on posterior samples generated using the Hamiltonian Markov Chain Monte Carlo method with 4 chains for 20,000 iterations with a burn-in period of 10,000. Interpretations were based on the median value (ES0.5: 0.5-quantile), the range within credible intervals (CrIs) and calculation of probabilities that the magnitude of the average effect size exceeded commonly used qualitative thresholds (e.g., small: 0.2, medium: 0.5, and large: 0.8) (25). Bayesian's CrIs can be interpreted probabilistically, such that with a 95% CrI, there is a 95% probability that the true (unknown) estimate would lie within the interval given the priors implemented and the evidence provided by the observed data. Additionally, the ES0.5 represents the center of the posterior such that values close to this point are generally more probable. Analyses were performed using the R wrapper package brms (example code presented in Appendix S4, Electronic Supplementary Material, https://links.lww.com/JSCR/A325) interfaced with Stan to perform sampling (19). Convergence of parameter estimates was obtained for all models with Gelman-Rubin R-hat values below 1.1 (39). All values presented in tables and figures include analyses conducted on data post removal of outliers, except for the association between controlled and no-exercise-controlled effect sizes presented in Figure 3, which include all data. Small-study effects (publication bias, etc.) were visually inspected with funnel plots and quantified with a multilevel extension of Egger's regression with effect sizes regressed on within-study variances and weights obtained from the reciprocal of the within- and between-study variances (34,71).

Results

Search Results

Figure 1 illustrates the studies identified and selected included based on the search strategy and screening process. A total of 139 studies were screened at full text and 84 excluded primarily because of sprint duration being greater than 30 seconds or sprints not completed at an “all out” intensity. A total of 55 studies were included in the review (11–14,25–27), (42–69), (69–89).

F1
Figure 1.:
PRISMA flow diagram detailing the results of each search and screening stage. A final number of 55 studies were included in the review.

Study Characteristics

Details of the 55 studies included in this review are shown in Table 1, with 25 (45%) of the studies including a nonexercise control group. Thirty studies (55%) comprised all male subjects, 2 studies (4%) comprised all female subjects, and 23 studies (41%) comprised both male and female subjects, with 3 of the studies reporting male and female data separately. In total, 589 subjects were allocated to a SIT intervention (median group size = 9 [IQR: 8–11]), with 257 subjects allocated to a nonexercise control group (median group size = 8 [IQR: 7–9]). Most studies (42 studies, 76%) recruited recreational subjects, with 10 studies (18%) recruiting sedentary subjects and 3 studies (6%) recruiting competitive athletes. In total, 617 outcomes were extracted demonstrating large variation in the number obtained from individual studies with the median equal to 7 (IQR: 3.5–15). Fifty percent of the outcomes were categorized as aerobic, whereas 12% were categorized as anaerobic and 38% categorized as mixed.

Table 1 - Overview of studies included in systematic review and meta-analysis.*
Author Aim SIT intervention population Study design Intervention variables Extracted outcomes Summary of findings Quality rating
Astorino et al. (2) To compare differences in adaptations to short-term high-intensity training in active men and women matched for age and V̇o 2max Recreational males (n = 11) and females (n = 9) Nonexercise control 2 wk (6 sessions), 4–6 × 30 s sprints, 300-s recovery, 7.5% BM resistance Peak power (W·kg−1), mean power (W·kg−1), and minimum power (W·kg−1), from a Wingate test;
o 2max (L·min−1; ml·kg−1·min−1), V̇co 2 (L·min−1), VE (L·min−1), O2 pulse at V̇o 2max (ml·beat−1), and RER from an incremental exercise test to exhaustion on a cycle ergometer
Similar improvements in power output and oxygen kinetics occurred between sexes matched for V̇o 2max and physical activity. 18/24
75%
Moderate
Babraj et al. (3) To determine if low-volume high-intensity interval exercise involving ∼250 kcal work improves glycemic control in sedentary young adults Sedentary males (n = 16) Nonexercise control 2 wk (6 sessions), 4–6 × 30 s sprints, 240-s recovery, 7.5% BM resistance 250 kJ cycle time trial (s) Low-volume high-intensity interval exercise increases glycemic control and 250 kJ cycle time trial performance increased 12/24
50%
Low
Bailey et al. (4) To determine the effect of work-matched repeated sprint training and endurance training on the kinetics of V̇o 2, HR, and muscle deoxygenation during moderate- and severe-intensity exercise and tolerance in recreationally active subjects Recreational males (n = 5) and females (n = 3) Exercise comparator (endurance training), and Nonexercise control 2 wk (6 sessions), 4–7 × 30 s sprints, 240-s recovery, 7.5% BM resistance Total work done (kJ) within each training session;
o 2peak (L·min−1; ml·kg−1·min−1), V̇o 2 (L·min−1), and work rate (W) at gas exchange threshold, and peak work rate (W) from an incremental exercise test to exhaustion on a cycle ergometer
o 2peak (L·min−1) and time to exhaustion (s) during a moderate and severe cycle step test
Repeated sprint training accelerated V̇o 2 kinetics during transitions to moderate and severe intensity exercise and enhanced exercise tolerance compared with endurance training 17/24
70.8%
Moderate
Barnett et al. (5) To compare enzymatic and histochemical adaptations to sprint training with sprint performance and exercise-induced changes in high-energy phosphagens, muscle glycogen, and lactate Recreational (n = 8) Nonexercise control 8 wk (24 sessions), 3–6 × 30 s sprints, 180-s recovery, 8.87 flywheel revolutions per pedal crank revolution gear ratio resistance o 2peak (L·min−1) from an incremental exercise test to exhaustion on a cycle ergometer
Peak power (W) and mean power (W) during 10-s sprint
Sprint training improved sprint and V̇o 2peak performance, and lowered net ATP degradation during sprint exercise 10/24
41.7%
Low
Bayati et al. (6) To compare the established SIT protocol versus a modified type of high-intensity training on both aerobic and anaerobic performance measures Recreational males (n = 8) Exercise comparator (sprint training at 125% power at V̇o 2max) and Nonexercise control 4 wk (12 sessions), 3–5 × 30 s sprints, 240-s recovery, 7.5% BM resistance o 2max (ml·kg−1·min−1) from an incremental exercise test to exhaustion on a cycle ergometer
Power at V̇o 2max (W), total work (kJ), and time to exhaustion at power at V̇o 2max (s) from a time to exhaustion at power at V̇o 2max test
Peak power (W), mean power (W), and total work (kJ) from a Wingate test
Aerobic and anaerobic performance similarly improved across both protocols, except for mean power output, which only improved within the SIT protocol 13/24
54.2%
Low
Benítez-Flores et al. (7) To determine the combined effects of resistance and sprint training, with very short efforts (5 s), on aerobic and anaerobic performances and cardiometabolic health-related parameters in young healthy adults Recreational males (n = 4) and females (n = 4) Exercise comparator (undulating periodized resistance training), and (concurrent resistance training and SIT), and nonexercise control 2 wk (6 sessions), 6–12 × 5 s sprints, 24-s recovery, 0.7 N·m resistance o 2max (ml·kg−1·min−1), power at V̇o 2max (W), and RERmax from an incremental exercise test to exhaustion on a cycle ergometer
Peak power (W), total work (kJ), and maximum pedalling rate (rpm) from 2 × 5 s sprints
countermovement jump (CMJ) height (cm)
Mean velocity (m·s−1), mean power (W), mean force (N) from an isoinertial squat test
Concurrent training promotes improvements in lower-body strength and aerobic capacity similar to resistance training and SIT interventions 21/24
87.5%
High
Broatch et al. (13) To determine the effects of regular postexercise cold water immersion on key markers of mitochondrial biogenesis following 6 wk of SIT Recreational males (n = 8) Exercise comparator (cold water immersion) 6 wk (18 sessions), 4–6 × 30 s sprints, 240-s recovery, 7.5–9.5% BM resistance 2 km cycle time trial (s) and mean power (W)
20 km cycle time trial (s), lactate threshold ,and peak aerobic power (W) from an intermittent graded exercise test; V̇o 2peak (ml·kg−1·min−1) from a steady-state cycle to fatigue at supramaximal power output
Cold water immersion administered following 6 wk of SIT had limited effects on endurance performance, mitochondrial biogenesis, or changes in mitochondrial content and function 19/24
79.2%
Moderate
Burgomaster et al. (15) To determine the effects of 6 sessions of SIT on muscle oxidative potential, V̇o 2peak, and endurance time to fatigue during cycling at an intensity equivalent to 80% V̇o 2peak Recreational males (n = 6) and females (n = 2) Nonexercise control 2 wk (6 sessions), 4–7 × 30 s sprints, 240-s recovery, 7.5% BM resistance O2 uptake (L·min−1), expired ventilation (L·min−1), RER, V̇o 2peak (ml·kg−1·min−1), and time to fatigue (min) from an incremental exercise test to exhaustion on a cycle ergometer
Peak power (W) and mean power (W) across 4 consecutive Wingate tests
SIT increased citrate synthase maximal activity and doubled endurance capacity during cycling exercise at 80% V̇o 2peak in recreationally active subjects 12/24
50%
Low
Burgomaster et al. (16) To determine the effects of 2 wk of SIT on carbohydrate metabolism during submaximal exercise Recreational males (n = 8) Nonexercise control 2 wk (6 sessions), 4–6 × 30 s sprints, 240-s recovery, 7.5% BM resistance Peak power (W) and mean power (W) from a Wingate test; 250 kJ time trial (s), and mean power (W)
o 2 (L·min−1) at 60% V̇o 2peak and 90% V̇o 2peak during a 2 stage cycling test
SIT decreased net muscle glycogenolysis and lactate accumulation, increased pyruvate oxidation capacity, and decreased 250 kJ time trial time 15/24
62.5%
Moderate
Burgomaster et al. (17) To determine the time course for adaptations in metabolite transport proteins following SIT Recreational males (n = 8) Nonexercise control 6 wk (18 sessions), 4–6 × 30 s sprints, 240-s recovery, 7.5% BM resistance 250 kJ cycle time trial (min) and mean power (W) Muscle oxidative potential and proteins associated with glucose and lactate/H+ transport, GLUT4 and MCT4, increased following 1 wk of SIT, and MCT1 increased following 6 wk of SIT 12/24
50%
Low
Burgomaster et al. (18) To compare the effects of endurance training and SIT on adaptations of metabolic markers Recreational males (n = 5) and females (n = 5) Exercise comparator (endurance training) 2 wk (6 sessions), 4–6 × 30 s sprints, 270-s recovery, ∼500 W resistance o 2peak (ml·kg−1·min−1; L·min−1) from an incremental exercise test to exhaustion on a cycle ergometer, and V̇o 2 (L·min−1), RER, and ventilation (L·min−1) at 65% V̇o 2max SIT elicits comparable adaptations in markers of skeletal muscle carbohydrate and lipid metabolism, and metabolic control, as endurance training despite a lower training duration 12/24
50%
Low
Camacho-Cardenosa et al. (22) To determine the effects of maximal intensity interval training in hypoxia in active adults Recreational subjects (n = 8) Exercise comparator (hypoxia), and nonexercise control 4 wk (8 sessions), 2 sets of 5 × 10-s sprints, 20–600 s recovery, no resistance stated o 2max (ml·kg−1·min−1), peak power (W), mean power (W), mean cadence (rpm), maximum torque (N·m) from a 3-min all-out test Eight sessions of maximal intensity interval training in hypoxia is enough to decrease the percentage of fat mass, improve hematocrit (HCT) and Hb parameters, and mean muscle power in healthy and active adults 15/24
62.5%
Moderate
Cochran et al. (23) To determine if β-alanine (ALA) supplementation or a placebo would improve physiological and performance adaptations following SIT Recreational males (n = 12) Exercise comparator (β-ALA supplement & SIT) 6 wk (18 sessions), 4–6 × 30 s sprints, 240-s recovery, 7.5% BM resistance o 2peak (ml·kg−1·min−1) and peak power (W) from an incremental exercise test to exhaustion on a cycle ergometer
250 kJ time trial mean power (W) and time (s)
Mean power (W) from a repeated Wingate test
SIT with β-ALA supplementation did not augment performance measures, training workload, or improvements in skeletal muscle oxidative capacity in comparison with a SIT with placebo intervention 19/24
79.2%
Moderate
Cocks et al. (24) To determine the effects of 6 wk of traditional endurance training and SIT on skeletal muscle microvascular density and microvascular enzyme content (eNOS and NOX2) in previously sedentary men Sedentary males (n = 8) Exercise comparator (endurance training) 6 wk (18 sessions), 4–6 × 30 s sprints, 270-s recovery, 7.5% BM resistance o 2peak (ml·kg−1·min−1), and peak aerobic power output (W) from an incremental exercise test to exhaustion on a cycle ergometer Muscle microvascular density and eNOS protein content increased following endurance training and sprint interval training in sedentary males 15/24
62.5%
Moderate
Creer et al. (26) To determine the effects of short term, high-intensity sprint training on the root-mean-squared and median frequency derived from electromyography (EMG), peak power, mean power, total work, and plasma lactate levels during a series of 30-s maximal sprints compared with endurance training alone in trained cyclists Competitive males (n = 10) Nonexercise control 4 wk (8 sessions), 4–10 × 30 s sprints, 240-s recovery, no resistance stated o 2max (L·min−1) from an incremental exercise test to exhaustion on a cycle ergometer
Peak power (W), mean power (W), and total work (kJ) from a Wingate test
SIT increased motor unit recruitment and total work compared with endurance training alone 12/24
50%
Low
Forbes et al. (36) To determine whether a short-term high-intensity interval cycling training program increases the rate of PCr recovery following moderate-intensity exercise in which pH changes are minimal Recreational males (n = 4) and females (n = 3) Nonexercise control 2 wk (6 sessions), 4–6 × 30 s sprints, 240-s recovery, 6.5–7.5% BM resistance Leg extension peak force (N)
Mean power (W) and mean peak power (W) in training sessions 1 and 6
Short-term SIT increases PCr recovery following moderate-intensity exercise, indicating an improvement in oxidative capacity 16/24
66.7%
Moderate
Gibala et al. (40) To compare changes in exercise capacity, and molecular and cellular adaptations in skeletal muscle after low-volume SIT and high-volume endurance training Recreational males (n = 8) Exercise comparator (endurance training) 2 wk (6 sessions), 4–6 × 30 s sprints, 240-s recovery, 7.5% BM resistance 750 kJ cycle time trial (s) and mean power (W); 50 kJ cycle time trial (s) and mean power (W) Low-volume SIT or traditional high-volume endurance training induced similar improvements in muscle oxidative capacity, muscle buffering capacity, and exercise performance 14/24
58.3%
Low
Gillen et al. (43) To determine whether SIT was a time-efficient exercise strategy to improve insulin sensitivity and other indices of cardiometabolic health to the same extent as traditional moderate-intensity continuous training Sedentary males (n = 9) Exercise comparator (moderate-intensity continuous training) and a nonexercise control 12 wk (31 sessions), 3 × 20 s sprints, 120-s recovery, 5% BM resistance o 2peak (ml·kg−1·min−1; L·min−1) and maximum workload (W) from an incremental exercise test to exhaustion on a cycle ergometer SIT improved insulin sensitivity, cardiorespiratory fitness, and skeletal muscle mitochondrial content to the same extent as moderate-intensity continuous training, despite a 5-fold lower exercise volume and training time commitment 18/24
75%
Moderate
Harmer et al. (46) To determine the effects of sprint training on respiratory, metabolic, and ionic perturbations during intense exercise conducted at an identical power output in 2 separate tests: one test matched for duration in pre- and posttraining trials and the other continued until exhaustion Recreational males (n = 7) No control 7 wk (21 sessions), 4–10 × 30 s sprints, 180–240-s recovery, 7.5% BM resistance Peak, mean, and relative expired ventilation (L·min−1), peak, mean, and relative O2 uptake (L·min−1), peak, mean, and relative CO2 output (L·min−1), peak RER, accumulated V̇o 2 (mmol.kg), total work (kJ) and time to exhaustion (s) from a test to exhaustion at 130% V̇o 2peak; V̇o 2peak (L·min−1), power output (W) and time to exhaustion (s) from an incremental exercise test to exhaustion on a cycle ergometer; peak power (W) and total work (kJ) from a 30-s all-out sprint Sprint training reduces metabolic and ionic perturbations within tissue during intense exercise matched for power output and work production, although indexes of anaerobic metabolism were not augmented during exhaustive exercise after training, despite the increased exercise duration, suggesting the importance of aerobic adaptations to performance after sprint training 7/19
36.8%
Very low
Harris et al. (47) To determine and compare the effects of work matched SIT with a less time committing sprint continuous protocol on brachial artery endothelial function, arterial stiffness, cardiorespiratory fitness, and circulating angiogenic cell number and function Recreational females (n = 6) Exercise comparator (sprint continuous training) 4 wk (12 sessions), 4 × 30 s sprints, 270-s recovery, 7.5% BM resistance o 2max (ml·kg−1·min−1; L·min−1), lactate threshold (ml·min−1·kg−1), peak work rate (W), and time (min) from an incremental step exercise test on a cycle ergometer Sprint continuous training improved cardiorespiratory fitness to a similar extent as SIT, with a trend for brachial artery flow-mediated dilation (FMD) increase following SIT but not sprint continuous training 18/24
75%
Moderate
Hazell et al. (48) To determine whether 10-s or 30-s SIT bouts with 2- or 4-min recovery periods can improve aerobic and anaerobic performance Recreational males (n = 6) and females (n = 6) in each of the 3 SIT groups Nonexercise control 2 wk (6 sessions), 4–6 × 30 s sprints, 240-s recovery, 100 g·kg−1·BM−1 resistance
2 wk (6 sessions), 4–6 × 10 s sprints, 240-s recovery, 100 g·kg−1·BM−1 resistance
2 wk (6 sessions), 4–6 × 10 s sprints, 120-s recovery, 100 g·kg−1·BM−1 resistance
o 2max (ml·kg−1·min−1) from an incremental exercise test to exhaustion on a cycle ergometer; 5-km time trial (s); peak power (W·kg−1) and mean power (W·kg−1) from a 30-s Wingate test The 10-s SIT protocols produced similar improvements in V̇o 2max and 5-km time trial performance compared with the established 30 s SIT protocol 14/24
58.3%
Low
Hommel et al. (49) To determine and compare the influence of SIT and endurance training on calculated power in maximal lactate steady state and maximal oxygen uptake. Recreational males (n = 10) Exercise comparator (endurance training), and nonexercise control 6 wk (18 sessions), 4–6 × 30 s sprints, 270 s recovery, 7.5% BM resistance o 2max (ml·min−1·kg−1) from an incremental exercise test to exhaustion on a cycle ergometer; power in lactate steady state (W); peak anaerobic power (W) from a modified sprint test. SIT and endurance training improve calculated power in maximal lactate steady state through differently influencing maximal lactate production rate and V̇o 2max. 15/24
62.5%
Moderate
Ijichi et al. (50) To compare the effects of sprint training on exercise performance between sprint training twice every second day and sprint training once daily, with the same total number of training sessions Recreational males (n = 20)
SIT once every day (n = 10)
SIT twice every second day (n = 10)
No control SIT daily: 5 d per week ×4 weeks (20 sessions), 3 × 30-s sprints, 10-min recovery, 5% BM resistance
SIT twice: 2–3 sessions per week × 4 wk (20 sessions total), 3 × 30-s sprints, 10-min recovery, 5% BM resistance
o 2max (ml·min−1·kg−1; L·min−1), peak aerobic power (W) and onset of blood lactate accumulation (W) from an incremental exercise test to exhaustion on a cycle ergometer
Time to fatigue (s) from a submaximal cycling test at 90% V̇o 2max
Peak power (W) and mean power (W) from 2 × 30 s maximal sprint tests
Similar improvements in peak and mean power output during 30-s sprint tests and anaerobic endurance capacity occurred between the groups, although SIT every second day improved the onset of blood lactate accumulation to a greater extent in physically active males 12/24
50%
Low
Ikutomo et al. (51) To determine the influence of inserted long rest periods during repeated sprint training on performance adaptations in competitive athletes Competitive male (n = 17) and female (n = 4) sprinters
Short recovery (n = 10)
Long recovery group (n = 11)
No control Short recovery: 3 wk (9 sessions), 2 sets of 12 × 6 s sprints, 24-s recovery, 20 min between the sets, 7.5% BM resistance
Long recovery: 3 wk (9 sessions), 2 sets of 12 × 6 s sprints, 24-s recovery—with an additional 7 min recovery every third sprint, 20 min between the sets, 7.5% BM resistance
o 2max (ml·min−1·kg−1) from an incremental exercise test to exhaustion on a cycle ergometer
Time to exhaustion (s) at 80% V̇o 2max
Peak power (W·kg−1) per sprint, 10 min, and 30 min following a repeated sprint test
Repeated sprint training with longer rest periods is an efficient strategy for improving power output compared with shorter rest periods alone 10/24
41.7%
Low
Jakeman et al. (52) To determine whether shorter-duration high-intensity training involving 6-s sprints and totalling 60 s of exercise per session could elicit improvements in performance Recreational males (n = 6) Nonexercise control 2 wk (6 sessions), 10 × 6 s sprints, 60-s recovery, 7.5% BM resistance Time to exhaustion (s) and the onset of blood lactate accumulation (s) from an incremental exercise test to exhaustion on a cycle ergometer; 10-km time trial (s); peak power output (W) for each training session Shorter duration SIT repeated over 2 wk improves aerobic performance and produces an attenuation of blood lactate accumulation normally seen with longer duration sprints or longer training interventions 11/24
45.8%
Low
Kavaliauskas et al. (53) To determine the effectiveness of cycling based high intensity training with different work-to-rest ratios for long-distance running. Competitive males (n = 14) and females (n = 18)
1:3 group: Males (n = 3) and females (n = 5)
1:8 group: Males (n = 3) and females (n = 5)
1:12 group: Males (n = 4) and females (n = 4)
Nonexercise control 1:3 group: 2 wk (6 sessions), 6 × 10 s sprints, 30 s recovery, 7.5% BM resistance
1:8 group: 2 wk (6 sessions), 6 × 10 s sprints, 80 s recovery, 7.5% BM resistance
1:12 group: 2 wk (6 sessions), 6 × 10 s sprints, 120 s recovery, 7.5% BM resistance
3 km running time trial (s);
o 2peak (ml·min−1·kg−1) and time to exhaustion (s) from an incremental exercise test to exhaustion on a cycle ergometer;
Peak power (W·kg−1) and mean power (W·kg−1) from a Wingate test
SIT with a lower work-to-rest ratio provides a sufficient training stimulus for improving running performance, with nonspecific training contributing to running performance in runners who regularly undergo endurance training. 12/24
50%
Low
Kavaliauskas et al. (54) To determine the effects of SIT on cardiorespiratory fitness and aerobic performance measures in young females Recreational females (n = 8) Nonexercise control (subjects acted as own controls) 4 wk (8 sessions), 4 × 30 s sprints, 240-s recovery, 7% BM resistance o 2peak (ml·min−1·kg−1) and time to exhaustion (s) from an incremental exercise test to exhaustion on a cycle ergometer
10-km time trial (s)
3-min critical power (W·kg−1)
Peak power (W), mean power (W), sum of peak power (W), and sum of mean power (W) during training sessions
SIT performed twice per week improves aerobic performance measures in young, untrained females 12/19
63.2%
Moderate
Larsen et al. (56) To determine the acute and short-term effects of high-intensity training on human skeletal muscle energetics in vivo using phosphorus magnetic resonance spectroscopy Recreational males (n = 8) No control 2 wk (6 sessions), 4–6 × 30 s sprints, 240-s recovery, 7.5% BM resistance o 2peak (ml·min−1·kg−1), time to exhaustion (s) and peak workload (W) from an incremental exercise test to exhaustion on a cycle ergometer
Knee extension maximal force (N)
Peak power (W) and mean power (W) during training sessions
6 sessions of high-intensity training alter in vivo muscle energetics likely contributing to increased exercise capacity 14/19
73.7%
Moderate
Lewis et al. (57) To determine the neuromuscular adaptations to SIT Recreational males (n = 7) No control 2 wk (6 sessions), 4–7 × 30 s sprints, 240-s recovery, 7.5% BM resistance 10-km time trial (s)
Peak power (W) and mean power (W) during training sessions
Quadriceps maximal voluntary contraction (N) pre and post sprints
SIT improved performance measures without measurable neuromuscular adaptations 18/24
75%
Moderate
Little et al. (60) To determine if sprint snacks increased V̇o 2peak and aerobic exercise performance in healthy individuals Recreational males (n = 14) and females (n = 14)
Sprint snacks: Males (n = 5) and females (n = 7)
Traditional SIT: Males (n = 9) and females (n = 7)
No control Sprint snacks:
6 wk (18 sessions), 3 × 20 s sprints, 1–4 h of recovery, 0.21 N m·kg−1 resistance
Traditional SIT: 6 wk (18 sessions), 3 × 20 s sprints, 180-s recovery, 0.21 N m·kg−1 resistance
o 2peak (ml·min−1·kg−1; L·min−1), peak power W), and time to exhaustion (min) from an incremental exercise test to exhaustion on a cycle ergometer
150 kJ time trial (min)
Peak power (W), mean power (W) and total work (kJ) across each training session
Sprint snacks improved V̇o 2peak, peak aerobic power, and 150 kJ time trial performance to the same extent as traditional SIT 19/24
79.2%
Moderate
Lloyd Jones et al. (62) To determine whether repeated 6-s sprint bouts with differing work-to-rest ratios resulted in different training adaptations Recreational males (n = 18) and females (n = 9)
1:8 group: Males (n = 6) and females (n = 3)
1:10 group: Males (n = 6) and females (n = 3)
1:12 group: Males (n = 6) and females (n = 3)
Nonexercise control 1:8 group: 2 wk (6 sessions), 10 × 6 s sprints, 48-s recovery, 7.5% BM resistance
1:10 group: 2 wk (6 sessions), 10 × 6 s sprints, 60-s recovery, 7.5% BM resistance
1:12 group: 2 wk (6 sessions), 10 × 6 s sprints, 72 s recovery, 7.5% BM resistance
10-km time trial (s)
Peak power (W), mean power (W), and session work (kJ) across each training session
All SIT conditions resulted in significant improvements in performance with no significant differences in improvement across any of the groups 12/24
50%
Low
McGarr et al. (64) To determine and compare any improvements in heat adaptation from short-term endurance training and SIT in moderately fit individuals Recreational males (n = 6) and females (n = 2) Exercise comparator (endurance training) 2 wk (8 sessions), 4–5 × 30 s sprints, 240-s recovery between each sprint, 7.5% BM resistance o 2peak (ml·kg−1·min−1) from an incremental exercise test to exhaustion on a cycle ergometer Short-term endurance and SIT
Improved aerobic fitness and attenuated cardiovascular strain during exercise in a hot environment, although neither training modality increased heat loss responses nor in minimized thermal strain
17/24
70.8%
Moderate
Metcalfe et al. (65) To determine the effects of a reduced exertion high-intensity training exercise intervention on insulin sensitivity and aerobic capacity Sedentary males (n = 7) and females (n = 8) Nonexercise control 6 wk (18 sessions), 2 × 10–20 s sprints, 200–220 s of recovery, 7.5% BM resistance o 2peak (L·min−1; ml·min−1·kg−1) from an incremental exercise test to exhaustion on a cycle ergometer SIT is associated with improved insulin sensitivity in sedentary young men and improved aerobic capacity in men and women 16/24
66.7%
Moderate
Metcalfe et al. (67) To determine whether there is a true sex difference in response to reduced exertion high-intensity interval training or if these findings can be explained by the large interindividual variability response inherent to all exercise training Sedentary males (n = 17) and females (n = 18) No control 6 wk (18 sessions), 1–2 × 10–20 s sprints, 200–220 s of recovery, 5% BM resistance o 2peak (ml·min−1·kg−1) and V̇o 2max (L·min−1; ml·min−1·kg−1) from an incremental exercise test to exhaustion on a cycle ergometer Reduced exertion high-intensity interval training presented substantial interindividual variability for all parameters with no sex differences evidenced 18/24
75%
Moderate
Muggeridge et al. (73) To determine the effects of dietary nitrate on the response to 3 wk of SIT Recreational males (n = 10) Exercise comparator (SIT with nitrate) and a nonexercise control 3 wk (9 sessions), 4–6 × 15 s sprints, 240-s recovery, 7% BM/5–10 air brake resistance o 2max (ml·min−1·kg−1), ventilatory threshold (W) and maximal workrate (W) from an incremental exercise test to exhaustion on a cycle ergometer
Peak power (W) and mean power (W) from each sprint within training sessions 1 and 9
SIT improved performance parameters, although no additional benefit was gained from the administration of dietary nitrate supplementation 18/24
75%
Moderate
Nalçakan (76) To determine and compare the effects of SIT and continuous endurance training on anthropometric, aerobic, and anaerobic performance indices, mechanical gross efficiency, blood lipids, inflammation, skeletal muscle damage, and myocardial cell injury in healthy young males Recreational males (n = 8) Exercise comparator (endurance training) 7 wk (21 sessions), 4–6 × 30 s sprints, 270-s recovery, 7.5% BM resistance Peak power (W), mean power (W), time to peak power (s), and power drop (%) from a Wingate test
Mechanical gross efficiency from a submaximal cycle test at 60% V̇o 2max
SIT improved body composition and performance measures to the same extent as continuous endurance training, although no changes occurred in lipid profile, serum levels of inflammatory markers, myocardial cell injury markers, or skeletal muscle damage markers following training 15/24
62.5%
Moderate
Nalçakan et al. (75) To determine whether reducing the sprint duration in the reduced exertion high-intensity training protocol from 20 to 10 s per sprint influences acute affective responses and the change in V̇o 2max following training Recreational males (n = 19) and females (n = 17)
20-s sprint group: Males (n = 8) and females (n = 10)
10-s sprint group: Males (n = 11) and females (n = 7)
No control group 20 s group: 6 wk (18 sessions), 2 × 10–20 s sprint, 220–240 s of recovery, 7.5% BM resistance
10 s group: 6 wk (18 sessions), 2 × 5–10 s sprint, 220–230 s of recovery, 7.5% BM resistance
o 2max (L·min−1) from an incremental exercise test to exhaustion on a cycle ergometer SIT involving 20- s sprints reported greater improvements in V̇o 2max compared with 10-s sprints 16/19
84.2%
High
O'Driscoll et al. (78) To determine the combined adaptations of the cardiac autonomic nervous system and myocardial functional and mechanical parameters to high-intensity interval training Sedentary males (n = 40) Nonexercise control (subjects acted as own controls) 2 wk (6 sessions), 3 × 30 s sprints, 120-s recovery, 7.5% BM resistance o 2peak (ml·min−1·kg−1; ml·min−1) and ventilatory equivalent (ml·min−1) from an incremental exercise test to exhaustion on a cycle ergometer SIT improves cardiac autonomic modulation, myocardial function, and myocardial mechanics 20/24
83.3%
High
Ørtenblad et al. (80) To determine the effects of 5 wk of sprint training on intermittent exercise performance, sarcoplasmic reticulum (SR) Ca2+ sequestration, and release function and SR ryanodine binding Recreational males (n = 9) Nonexercise control 5 wk (15 sessions), 20 × 10 s sprints, 50-s recovery, 8.25% BM resistance o 2peak (ml·min−1·kg−1) from an incremental exercise test to exhaustion on a cycle ergometer
Total work (kJ) and mean power (W·kg−1) from a 10 × 8 s sprint test
Mean power (W·kg−1) across each training session sprint and each second of each sprint
High-intensity intermittent training increases the peak rate of AgNO3-stimulated SR Ca2+ release 12/24
50%
Low
Parra et al. (81) To determine the effect of 2 different SIT protocols on muscle metabolic response and performance Recreational males (n = 10)
No recovery program (n = 5)
Two-day recovery program (n = 5)
SIT groups only 2 wk (14 sessions), 4–14 × 15–30 s sprints, 45 s to 12 min of recovery between sprints, 7.5% BM resistance (no recovery days between sessions)
6 wk (14 sessions), 4–14 × 15–30 s sprints, 45 s to 12 min of recovery between sprints, 7.5% BM resistance (2 days recovery between sessions)
Peak power (W) and mean power (W) from a Wingate test During high-intensity training, shorter rest periods between sessions induced greater biochemical adaptations in human muscle compared with longer rest periods 11/24
45.8%
Low
Rakobowchuk et al. (82) To determine whether 6 wk of high-intensity, low-volume, SIT improves central (carotid) artery distensibility, peripheral (popliteal) artery distensibility and endothelial function in the trained legs to the same extent as high-volume, moderate-intensity endurance training Sedentary males (n = 5) and females (n = 5) Exercise comparator (endurance training) 6 wk (18 sessions), 4–6 × 30 s sprints, 270-s recovery, 7.5% BM resistance o 2peak (ml·min−1·kg−1) from an incremental exercise test to exhaustion on a cycle ergometer, peak power output (W) from a Wingate test SIT elicits similar improvements in peripheral vascular structure and function to endurance training, although central artery distensibility may require a longer training stimuli or greater initial vascular stiffness 14/19
73.7%
Moderate
Richardson and Gibson (84) To determine the effects of hypoxic SIT on aerobic capacity Recreational males (n = 6) and females (n = 3) Nonexercise control 2 wk (6 sessions), 4–7 × 30 s sprints, 240-s recovery, 7.5% BM resistance o 2peak (L·min−1) from an incremental exercise test to exhaustion on a cycle ergometer, time to exhaustion (min) from an incremental exercise test to exhaustion on a cycle ergometer at 80% V̇o 2peak power output, and mean power output (W·kg−1) across the first 4 sprints in sessions 1 and 6 o 2peak and time to exhaustion improved following hypoxic and normoxic SIT compared with a control, although hypoxia did not provide any additional improvements in endurance performance 13/24
54.2%
Low
Rodas et al. (85) To determine the changes in aerobic and anaerobic metabolism produced by a new incremental training program of “all-out” loads, repeated daily for 2 wk, and with long recovery periods Recreational males (n = 5) No control 2 wk (14 sessions), 4–14 × 15–30 s sprints, 45–720 s of recovery, 7.5% BM resistance o 2 (ml·kg−1·min−1) and power output (W) from an incremental exercise test to exhaustion on a cycle ergometer, V̇o 2 (ml·kg−1·min−1) and peak and mean power output (W) from a Wingate test, and pedalling rate (rpm) across each training session Enzymatic activities of energetic pathways improve in a short time following short-duration, high-load, and long recovery period “all-out” sprints 9/19
47.4%
Low
Scalzo et al. (88) To determine changes in endurance exercise performance after SIT and to measure the integrated muscle protein synthesis response, mitochondrial biogenesis, and proteome kinetics in males and females over the course of 3 wk of SIT. Recreational males (n = 11) and females (n = 10) No control 3 wk (9 sessions), 4–8 × 30 s sprints, 240-s recovery, 7.5% BM resistance o 2max (ml·kg−1·min−1) from an incremental exercise test to exhaustion on a cycle ergometer, 40-km time trial (s) and mean power output (W; W·kg−1 fat free mass) across each sprint for sessions 1 and 9 Greater synthesis rates of muscle protein synthesis and mitochondrial biogenesis were observed in males than females during SIT, although there were no differences in V̇o 2max, time trial or power output when normalized to fat free mass 12/19
63.2%
Moderate
Schlittler et al. (89) To determine the effects of 3 weeks of SIT on high-intensity cycling performance, ryanodine receptor modifications, and the recovery of isometric force in recreationally active human subjects Recreational males (n = 8) No control 3 wk (9 sessions), 4–6 × 30 s sprints, 240-s recovery, 0.7 N·m·kg−1·BM−1 resistance Maximal power (W) from an incremental exercise test to exhaustion on a cycle ergometer
Total work (kJ) and peak power (W·kg−1) across 6 Wingate cycles
Isometric knee extension maximal voluntary contraction (N) pre and post training session
SIT did not accelerate the recovery of isometric force, although did provide incomplete protection against RyR1 alteration 10/19
52.6%
Low
Shenouda et al. (91) To determine the effects of 6 and 12 wk of moderate-intensity continuous training and low-volume SIT on brachial and popliteal artery endothelial function and diameter, and central and lower limb arterial stiffness in sedentary, healthy men compared with nontraining controls Sedentary males (n = 9) Exercise comparator (moderate-intensity continuous training), and a nonexercise control 12 wk (31 sessions), 3 × 20 s sprints, 120-s recovery, 5% BM resistance o 2peak (ml·kg−1·min−1) from an incremental exercise test to exhaustion on a cycle ergometer Brachial artery responses to SIT may follow a different time course not captured by a 6- and 12-wk intervention, although these are observed with moderate-intensity continuous training 17/24
70.8%
Moderate
Shepherd et al. (92) To determine whether SIT induces improvements in insulin sensitivity and net intramuscular triglyceride (IMTG) breakdown and to investigate the underlying mechanisms Sedentary males (n = 8) Exercise comparator (endurance training) 6 wk (18 sessions), 4–6 × 30 s sprints, 270-s recovery, 7.5% BM resistance o 2peak (L·min−1; L·kg−1·min−1) and peak Workload (W) from an incremental exercise test to exhaustion on a cycle ergometer, and V̇o 2 (L·min−1), V̇co 2 (L·min−1) and RER from a 60 min cycle at 65% V̇o 2peak 6 wk of SIT and endurance training improve insulin sensitivity through mechanisms involved with increased PLIN2, PLIN5, and IMTG utilization during exercise 17/19
89.5%
High
Songsorn et al. (95) To determine whether a single 20-s cycle sprint per training session can provide a sufficient stimulus for improving V̇o 2max Recreational males (n = 5) and females (n = 10) Nonexercise control 4 wk (12 sessions), 1 × 20 s sprints, 7.5% BM resistance o 2max (L·min−1) and peak power output (W) from an incremental exercise test to exhaustion on a cycle ergometer A single 20-s cycle sprint per training session is not a sufficient stimulus for improving V̇o 2max. 20/24
83.3%
High
Terada et al. (103) To determine the effects of SIT with exogenous carbohydrate supplementation and SIT following overnight fast on aerobic capacity and high-intensity aerobic endurance Recreational males (n = 11) Exercise comparator (SIT with exogenous carbohydrate) 4 wk (12 sessions), 4–7 × 30 s sprints, 240-s recovery, 7.5% BM resistance o 2peak (ml·O2 −1·kg−1·min−1) from an incremental exercise test to exhaustion on a cycle ergometer, cycling time to exhaustion (s) at 85% V̇o 2peak, and mechanical work (Joules·kg−1) and peak power output (W·kg−1) across each training week Fasted SIT compromises exercise intensity and volume but can increase the ability to sustain high-intensity aerobic endurance exercise compared with SIT with exogenous carbohydrate supplementation 19/19
100%
High
Thompson et al. (104) To determine the independent and combined performance and physiological effects of SIT and NO3 - supplementation during a 4 wk intervention. Recreational males (n = 6) and females (n = 6) Nonexercise control (with concurrent NO3 - beetroot juice) and exercise comparator (SIT with concurrent NO3 - beetroot juice) 4 wk (14 sessions), 4–5 × 30 s sprints, 240 s recovery, 7.5% BM resistance o 2peak (L·min−1) and peak work rate (W) from an incremental exercise test to exhaustion on a cycle ergometer, and V̇o 2peak (L·min−1) and work rate (W) at gas exchange threshold NO3 - supplementation reduced the O2 cost of submaximal exercise, resulting in a greater improvement in incremental exercise performance and muscle metabolic adaptations to training compared with a placebo. 18/19
94.7%
High
Thompson et al. (105) To compare the physiological and exercise performance adaptations to 4 wk of SIT accompanied by concurrent supplementation with NO3 - beetroot juice, or potassium NO3 - or SIT undertaken without dietary NO3 -. Recreational males (n = 6) and females (n = 6) Exercise comparators (SIT with concurrent NO3 - beetroot juice) and (SIT with concurrent potassium NO3 -) 4 wk (14 sessions), 4–5 × 30 s sprints, 240 s recovery, 7.5% BM resistance o 2peak (L·min−1) and peak work rate (W) from an incremental exercise test to exhaustion on a cycle ergometer, V̇o 2peak (L·min−1) and time to task failure (s) during a moderate and severe cycle step test 4 wk of sprint interval training with concurrent NO3 - beetroot juice supplementation results in greater exercise capacity adaptations compared with sprint interval training alone or sprint interval training with concurrent potassium NO3 - supplementation. 19/19
100%
High
Vera-Ibanez et al. (106) To determine the neural adaptations associated with a low-volume Wingate-based high-intensity interval training Recreational males (n = 7) Nonexercise control 4 wk (12 sessions), 3–6 × 30 s sprints, 240-s recovery, 7.5% BM resistance Peak power (W; W·kg−1) from a Wingate test, plantar flexor maximum voluntary contraction (MVC) (N) on a soleus isolation machine Wingate-based training increased peak power and higher spinal excitability, with no changes in volitional wave or MVC 14/24
58.3%
Low
Yamagishi et al. (111) To determine the time course of training adaptations to 2 different SIT programs with the same sprint: Rest ratio (1:8) but different sprint duration Recreational males (n = 13) and females (n = 5)
15-s sprint group (n = 9) males (n = 7) and females (n = 2)
30-s sprints group (n = 8) males (n = 5) and females (n = 3)
Nonexercise control 9 wk (18 sessions), 4–6 × 15 s sprints, 120 s recovery, 7% BM resistance
9 wk (18 sessions), 4–6 × 30 s sprints, 240 s recovery, 7% BM resistance
o 2peak (ml·min−1·kg−1; L·min−1), O2 pulse (ml·beat−1·kg−1) and time to exhaustion (s) from an incremental exercise test to exhaustion on a cycle ergometer, 10 km time trial (s), critical power (W) from a 3-min critical power test, peak power output (W·kg−1) and total work (kJ) across training sessions 6, 12 and 18. A 50% reduction in sprint duration does not diminish overall training adaptations over 9 wk, although cardiorespiratory function plateaus within several weeks of sprint interval training with endurance capacity more sensitive to training over a longer timeframe. 13/24
54.2%
Low
Yamagishi et al. (112) To determine the effects of recovery intensity on endurance adaptations during SIT. Recreational males (n = 9) and females (n = 5)
30 s sprints group (n = 7) males (n = 4) and females (n = 3)
Recreational males (n = 5) and females (n = 2)
No control 2 wk (6 sessions), 4–6 × 30 s sprints, 240-s active recovery at 40% V̇o 2peak, 7.5% BM resistance
2 wk (6 sessions), 4–6 × 30 s sprints, 240-s passive recovery, 7.5% BM resistance
o 2peak (ml·min−1·kg−1; L·min−1) and peak power (W) from an incremental exercise test to exhaustion on a cycle ergometer
10-km cycle time trial (s)
Critical power (W) from a 3-min critical power test
Total work (kJ), peak V̇o 2peak (L·min−1) and mean V̇o 2peak (L·min−1) for total test and across every 30 s from a 3-min critical power test
Total work (kJ), peak power (W·kg−1), peak and mean power reproducibility (%) across every training session
Mean V̇o 2 (L·min−1) over 4 sprints, and 4 rest periods within sessions 1 and 6
Greater endurance adaptations occurred with active recovery when performing SIT over a short time frame, without increasing total training commitment time 10/24
41.7%
Low
Zelt et al. (113) To determine the effect of reducing SIT work interval duration on increases in maximal and submaximal performance Recreational males (n = 23)
30-s sprint group (n = 11)
15-s sprint group (n = 12)
Exercise comparator (endurance training) 4 wk (12 sessions), 4–6 × 30 s sprints, 270-s recovery, 7.5% BM resistance
4 wk (12 sessions), 4–6 × 15 s sprints, 285-s recovery, 7.5% BM resistance
o 2peak (ml·min−1), lactate threshold (mmol·L−1), relative lactate threshold (%V̇o 2peak) and peak O2 pulse (mlO2·beat−1), from an incremental exercise test to exhaustion on a cycle ergometer, peak power (W), and mean power (W) from a Wingate test, critical power (W) from a 3-min critical power test Reducing SIT work interval from 30 to 15 s does not impact training-induced increases in either aerobic or anaerobic power, absolute lactate threshold, or critical power 15/19
78.9%
Moderate
*SIT = sprint interval training; BM = body mass; RER = respiratory exchange ration; PCr = phosphocreatine.

Methodological Quality

The overall quality ratings and ratings across the 4 domains evaluated are presented in Table 2. The mean (±SD) percentage quality rating score was 63% for comparator studies and 56% for noncomparator studies (Table 2). Quality ratings were highest for the reporting domain with all studies clearly describing characteristics of subjects and providing estimates of random variability in the data. Reporting of the number of sessions attended and a minimum number of sessions for inclusion were identified as important requirements given the small number of sessions typically performed and the subsequent influence this could have on estimates of effectiveness. It was identified that less than half of studies (44 and 41%, respectively) reported this information.

Table 2 - Overall and domain specific methodological quality ratings.
Research design Reporting Internal validity bias Internal validity confounding Statistical power Overall rating
Comparator 80% 43% 67% 10% High: 6%
Moderate: 51%
Low: 43%
Noncomparator 78% 43% 49% 11% Moderate: 50%
Low: 33%
Very low: 17%
Both comparator and noncomparator 79% 43% 63% 11% High: 6%
Moderate: 50%
Low: 42%
V. Low: 2%

Following reporting, the domain with the highest-quality ratings was internal validity—confounding. Within this section, the highest scoring item (94%) was “were the subjects in different intervention groups recruited from the same population,” and the lowest scoring item (49%) was “were losses of subjects to follow-up taken into account?” As part of the methodological evaluation, the present review also considered studies use of familiarization for both SIT sessions and outcome assessment methods because these were identified as important sources of bias. Evaluation showed that 39% of studies included familiarization sessions for training sessions, and 53% of studies included familiarization sessions for outcome assessments. Finally, only 9 studies demonstrated a priori sufficient power for their statistical analysis (7,24,47,57,60,66,75,89,95). Additionally, only 3 of these studies adjusted power calculations to account for inclusion of multiple outcome variables (24,89,95).

Training Intervention Description

Most interventions were very short in duration, with 17 studies (31%) comprising interventions of 2 weeks, a total of 32 studies (58%) comprising interventions of 4 weeks or less, and the longest duration equal to 12 weeks. To describe the training interventions implemented, selected training data were extracted and summary statistics calculated to quantify frequency, intensity, volume, energy system specificity, and periodization. Training frequency was quantified by extracting the number of sessions performed per week. The most common training frequency employed across the studies was 3 training sessions per week (43 studies, 78%), with a range from 2 (6 studies, 11%) to 7 (2 studies, 4%).

The intensity of the training stimulus was quantified by the external resistance applied during cycling and the average duration of sprints performed (shorter duration sprints characterized by higher intensities). Forty-seven studies (85%) reported applying external resistance as a percentage of body mass. Of these studies, 8 (17%) applied loads less than 7.5% of body mass (as low as 5% body mass), 37 (79%) applied a load equal to 7.5% of body mass, and 2 (4%) applied a load up to 9.5% of body mass. Similarly, a standard value was frequently applied to sprint duration, with 37 studies (67%) including average sprint durations of 30 seconds. The percentage of studies that included average sprint durations up to 10 seconds, between 10 and 20 seconds, and between 20 and 30 seconds was equal to 13, 16, and 4%, respectively.

The volume of training was quantified by the average number of sprints per session and total sprint time per session. Eighteen studies (33%) included interventions comprising on average between 1 and 4 sprints per session, approximately half (28 studies 51%) comprising 5 or 6 sprints per session, and 9 studies (16%) comprising 6 or more with a maximum of 24. Total sprint time per session ranged from 17.5 to 210 seconds, with a median value of 150 seconds (IQR: 75–150 seconds). Energy system specificity was quantified by calculating work-to-rest ratios, with values across studies ranging from 1:100 to 1:3, with a median ratio of 1:8 (IQR: 1:9 to 1:8). Finally, the extent to which interventions employed periodization was quantified by examining variation in training frequency, volume, and intensity. Only 4 studies (7%) altered training frequency, and only 5 studies (9%) altered intensity (as quantified by sprint duration). In contrast, most studies (41 studies, 75%) included variation in training volume, calculated by differences in the number of sprints performed each session. In those studies that included variation, the median absolute change in the number of sprints was 2 (IQR: 2–3), with values ranging from 1 to 10. Periodization models altering training volume tended to be simple and included linear increases in the number of sprints performed per session. Several studies integrated a taper week through a decreased sprint number before postintervention testing.

Meta-Analysis

Of the 619 outcomes selected for extraction, 436 outcomes from 52 studies included sufficient before and after data from sprint intervention groups to be included in the meta-analysis. In contrast, only 114 outcomes from 24 studies included sufficient data from both sprint and a no-exercise control group to be included in sensitivity analyses. The primary meta-analysis conducted across all outcome types estimated a medium pooled effect demonstrating improved physical performance following SIT intervention (ES0.5 = 0.52 [95% CrI: 0.42–0.62]; Figure 2). Relatively large between-study variance was identified τ0.5 = 0.32 (75% CrI: 0.27 to 0.38) with central estimates indicating very low intraclass correlation ICC0.5 = 0.02 (75% CrI: 0.00–0.09) of multiple outcomes reported within the same studies. When categorized by outcome type, the analysis provided some evidence of differences. The greatest effects were obtained for anaerobic outcomes (ES0.5 = 0.61 [95% CrI: 0.48–0.75]), followed by mixed aerobic-anaerobic (ES0.5 = 0.50 [95% CrI: 0.30–0.70]) and aerobic (ES0.5 = 0.49 [95% CrI: 0.39–0.60]) outcomes. Sensitivity analyses of the main meta-analytic findings were conducted with effect sizes adjusted for no-exercise control group data. Initial assessment comparing both noncontrolled and no-exercise-controlled effect sizes demonstrated a close association (Figure 3) with a small positive bias identified for noncontrolled effect sizes (β0:0.5 = 0.09 [95% CrI: −0.04 to 0.23]; β1:0.5 = 1.00 [95% CrI: 0.94–1.07]; Figure 3). Sensitivity analyses conducted for the pooled data and split by outcome category resulted in no substantive changes (Table 3).

F2
Figure 2.:
Bayesian’s forest plot of multilevel meta-analysis conducted on noncontrolled effect sizes. Results from individual studies represent shrunken estimates based on the random effects model fitting and borrowing of information across studies to reduce uncertainty. Circles represent the pooled estimate from individual studies and across studies (average), generated with Bayesian’s inference along with the 95% credible intervals (95% CrI). Positive values describe improvements in outcomes based on SIT intervention. SIT = sprint interval training.
F3
Figure 3.:
Comparison of noncontrolled and no-exercise-controlled effect sizes. Solid line is the unity line, and dashed line is the best fit line illustrating positive bias of noncontrolled effect sizes.
Table 3 - Results from primary analyses conducted on noncontrolled effect sizes and sensitivity analyses conducted on controlled effect sizes from studies including nonexercise control groups.*
Analysis Analysis details Effect size/probability of medium effect Sensitivity analysis Sensitivity analysis details Effect size/probability of medium effect
Noncontrolled effect sizes: all outcomes 432 effect sizes from 52 studies (mode quality = moderate: 50%) 0.52 [95% CrI: 0.42–0.62; d ≥ 0.5: Pr = 64%] Controlled effect sizes: all outcomes 111 effect sizes from 24 studies (mode quality = low: 58%) 0.51 [95% CrI: 0.27–0.76; d ≥ 0.5: Pr = 55%]
Noncontrolled effect sizes: aerobic outcomes 259 effect sizes from 49 studies (mode quality = moderate: 51%) 0.49 [95% CrI: 0.39–0.60; d ≥ 0.5: Pr = 41%] Controlled effect sizes: aerobic outcomes 76 effect sizes from 22 studies (mode quality = low: 50%) 0.45 [95% CrI: 0.32–0.70; d ≥ 0.5: Pr = 39%]
Noncontrolled effect sizes: anaerobic outcomes 59 effect sizes from 20 studies (mode quality = low: 50%) 0.61 [95% CrI: 0.48–0.75; d ≥ 0.5: Pr = 93%] Controlled effect sizes: anaerobic outcomes 23 effect sizes from 8 studies (mode quality = low: 63%) 0.59 [95% CrI: 0.21–0.91; d ≥ 0.5: Pr = 73%]
Noncontrolled effect sizes: mixed aerobic-anaerobic outcomes 114 effect sizes from 18 studies (mode quality = moderate: 53%) 0.50 [95% CrI: 0.30–0.70; d ≥ 0.5: Pr = 50%] Controlled effect sizes: mixed aerobic-anaerobic outcomes 12 effect sizes from 2 studies (mode quality = moderate: 50%) 0.40 [95% CrI: = 0.12–0.726; d ≥ 0.5: Pr = 32%]
*Effect sizes are magnitude-based standardized mean differences.
Results are from multilevel random effects models with median parameter estimates and 95% credible intervals (95% CrI). Pr expresses the proportion of the pooled effect size posterior sample that is greater or equal to a moderate effect (d ≥ 0.5).

Meta-regressions were performed to assess the effects of demographic factors and training-related variables on pooled effect sizes. An initial meta-regression was performed across all outcome types to assess the effect of intervention duration with time in weeks included as a covariate. It was estimated that the pooled effect size increased by 0.03 per week (β1: ES0.5 = 0.03 [95% CrI: 0.00–0.06]), with the covariate added to all subsequent meta-regressions. Substantive variation was identified in the number of outcomes extracted across sedentary (23), recreationally active (350), and competitive (31) populations. No clear population differences were obtained for pooled effects sizes obtained in a meta-regression across all outcomes types, with large uncertainty in estimates identified (βrecreational:competitive: ES0.5 = 0.21 [95% CrI: −0.20 to 0.61], βrecreational:sedentary: ES0.5 = 0.13 [95% CrI: −0.16 to 0.38]).

The effects of training-related variables were assessed pooling across all outcomes while controlling for intervention duration and outcome type (through inclusion of fixed effects) and were assessed for each outcome separately (Table 4). To assess the influence of training intensity, meta-regressions were performed separately with sprint duration and external load expressed as categorical variables. Sprint duration was categorized as short (5–10 seconds), medium (10–20 seconds), and long (+20 seconds). Pooled effects sizes obtained across all outcomes provided evidence of a reduced effect with short-duration sprints (βlong:short: ES0.5 = −0.15 [95% CrI: −0.42 to 0.08]), and no evidence of a difference between medium and long (βlong:mid: ES0.5 = 0.04 [95% CrI: −0.12 to 0.19]) duration. External load was expressed as a binary variable and categorized as low (≤7% body mass) and high (+7% body mass). Results indicated a similar pooled effect size irrespective of the external load (βhigh:low: ES0.5 = −0.10 [95% CrI: −0.30 to 0.18]).

Table 4 - Results from meta-regressions conducted on training variables across all outcomes and individual outcome categories.*
All outcomes ES0.5 [95% CrI] Aerobic ES0.5 [95% CrI] Mixed ES0.5 [95% CrI] Anaerobic ES0.5 [95% CrI]
Training intensity
 Sprint duration
  Long (+20 s): short (5–10 s) −0.15 [−0.42 to 0.08]
Number of effects: (302/75)
−0.24 [−0.51 to −0.01]
Number of effects: sizes: (195/25)
−0.02 [−0.44 to 0.66]
Number of effects: (58/42)
−0.26 [−0.96 to 0.44]
Number of effects: (49/8)
  Long (+20 s): medium (10–20 s) 0.04 [−0.12 to 0.19]
Number of effects: (302/55)
−0.03 [−0.21 to 0.15]
Number of effects: (195/39)
0.22 [−0.19 to 0.64]
Number of effects: (58/14)
Analysis not completed because of sample size
 External load
  High (>7% BM): low (≤7% BM) −0.10 [−0.30 to 0.18]
Number of effects: (311/79)
−0.10 [−0.44 to 0.22]
Number of effects: (186/47)
−0.10 [−0.82 to 0.68]
Number of effects: (78/32)
Analysis not completed because of sample size
Training volume
 No. of sprints per session
  High (+6 sprints): medium (5–6 sprints) −0.14 [−0.42 to 0.12]
Number of effects: (97/280)
−0.06 [−0.40 to 0.27]
Number of effects: (41/174)
−0.22 [−0.61 to 0.10]
Number of effects: (42/64)
−0.19 [−0.52 to 0.15]
Number of effects: (14/42)
  High (+6 sprints): low (1–4 sprints) −0.20 [−0.51 to 0.13]
Number of effects: (97/55)
−0.16 [−0.47 to 0.14]
Number of effects: (41/44)
−0.39 [−0.71 to 0.15]
Number of effects: (42/8)
Analysis not completed because of sample size
 Total sprint time per session (standardised) 0.05 [0.00 to 0.11]
Number of effects: 432
0.05 [−0.05 to 0.11]
Number of effects: 259
0.07 [−0.21 to 0.34]
Number of effects: 114
−0.04 [−0.29 to 0.20]
Number of effects: 59
Work-to-rest ratio
 Work-to-rest ratio (standardized) −0.00 [−0.06 to 0.06]
Number of effects: 432
0.06 [−0.01 to 0.12]
Number of effects: 259
−0.03 [−0.35 to 0.29]
Number of effects: 114
−0.08 [−0.19 to 0.04]
Number of effects: 59
*BM = body mass.
Effect sizes are magnitude-based standardized mean differences.
Results are from multilevel random effects models with median parameter estimates and 95% credible intervals [95% CrI].

To assess the influence of training volume, meta-regressions were performed separately with the number of sprints performed in each session expressed as categorical variable and total sprint time per session expressed as a covariate. Number of sprints performed in each session were categorized as low (1–4 sprints), medium (5–6 sprints), and high (+6 sprints). Pooled effects sizes obtained across all outcomes provided evidence of an increased effect with higher volume, reflected in both the high versus medium (βhigh:medium: ES0.5 = −0.14 [95% CrI: −0.42 to 0.12]) and high versus low (βhigh:low: ES0.5 = −0.20 [95% CrI: −0.51 to 0.13]) comparisons. Similarly, results demonstrated greater effects with increased total sprint time per session. The median estimate obtained using all outcome types indicated a 0.05 increase in pooled effect size for each standard deviation increase in total sprint time per session (β1: ES0.5 = 0.05 [95% CrI: 0.00–0.11]).

The final training variable assessed was work-to-rest ratio. The analysis conducted across all outcome variables identified no evidence of a change in pooled effect size when expressed in standard deviation units (β1: ES0.5 = −0.00 [95% CrI: −0.06 to 0.06]). However, when the analysis was conducted on individual outcome types, the results indicated that lower work-to-rest ratios were more effective for aerobic outcomes, and increased work-to-rest ratios were more effective for anaerobic outcomes (Table 4). Meta-regressions performed for work-to-rest ratio were the only analyses that demonstrated clear evidence of contrasting results across outcome types (Table 4).

Small Study Effects

Evidence of extensive small study effects were identified visually from funnel plot asymmetry of noncontrolled effect sizes (Figure 4) and through the multilevel extension of Egger's regression (β0: ES0.5 = −0.77 [95% CrI: −0.90 to −0.64]). Results demonstrated that studies with small subject numbers (n ≤ 10) were much more likely to report very large effect sizes (ES > 1) but rarely reported small or negative effect sizes.

F4
Figure 4.:
Funnel plot of noncontrolled effect sizes and their standard errors. Highlighted blue region illustrates pooled effect size estimate and 95% credible interval. Red line illustrates a null effect.

Discussion

The aim of this review was to quantify the effects of SIT and potential moderators on a range of physical performance measures using aggregate data from published studies. The results demonstrated that healthy individuals engaging in SIT were most likely to experience moderate improvements across a range of physical performance outcomes. The largest pooled effect size was estimated for anaerobic outcomes; however, effect estimates were also similar for aerobic and mixed aerobic-anaerobic outcomes. Substantive variation in training protocols was identified with regards to primarily sprint duration (intensity) and the number of sprints performed (volume). The results from meta-regressions identified that intervention protocols with longer sprint durations and more sprints resulted in greater improvements. Most interventions included were very short in duration, with 17 studies (31%) comprising interventions of 2 weeks and 32 studies (58%) comprising interventions of 4 weeks or less. Collectively, the findings indicate that SIT training can improve a range of performance outcomes dependent on both the aerobic and anaerobic energy systems over short intervention periods, indicating that the training strategy may be effective for improving sport performance and provide multiple opportunities to include the training within broader training plans. However, it is noteworthy that only 6% of the data included in the analysis were obtained from competitive athletes, which limits application of findings to this population. Additionally, analysis of methodological quality of studies and identification of extensive small study effects indicates limitations of the research base that likely overestimates the effectiveness of interventions and suggests areas for future development.

The finding that SIT interventions generate medium effects on physical performance outcomes is consistent with previous meta-analyses. Sloth et al. (94) and Gist et al. (44) reported pooled effects sizes of 0.69 and 0.63, respectively, for intervention only and nonexercise-controlled comparisons. In the present review, Bayesian meta-analyses were conducted generating posterior distributions for pooled effect sizes that can be readily interpreted probabilistically. Across all outcomes, the present review estimated a median pooled effect size of 0.52 with the probability that the value was greater than small (d ≥ 0.2) almost equal to 1 and the probability that the value was greater than medium (d ≥ 0.5) equal to 0.64. The quality rating of the included studies generating this overall outcome estimate was moderate. In agreement with previous reviews, the findings of the current meta-analysis identified the existence of potential moderators. Weston et al. (110) reported that subjects initial training status was the most influential moderator with the largest pooled effects estimated for sedentary individuals. In the current review, there was a large skew toward studies conducted with recreationally active subjects (76%) compared with sedentary subjects (18%) or competitive athletes (6%). No clear population differences were identified for the pooled effect size. In the current meta-analysis, there were overlaps in effect estimates between the 3 outcome domains, with central values indicating that the largest values were obtained for anaerobic outcomes (Table 3). The most common measures included in this category were related to anaerobic power (e.g., peak power) and capacity (e.g., mean power, total work). Improvements in anaerobic fitness following SIT can be attributed to improvements in both anaerobic and aerobic metabolism. Previous research has demonstrated a range of enzymatic adaptations to SIT including increased activity in creatine kinase and key glycolytic enzymes, such as phosphofructokinase, lactate dehydrogenase, glycogen phosphorylase, and aldose (58,81). Additionally, research has established that adaptations to SIT can include greater muscular glycogen concentration and enhanced muscle buffering capacity (17,81). Across sprint durations representative of SIT (i.e., 6–30 seconds), the contributions of phosphocreatine (PCr) and anaerobic glycolysis to ATP turnover are similar (11,38,96), leading to consistent increases in peak and mean power outputs. The ability to sustain a higher power output following SIT indicates greater fatigue resistance and enhanced exercise capacity (36). However, the anaerobic adenosine triphosphate (ATP) utilization rate is reduced during the second half of a 20-second sprint when compared with the first half (12). Therefore, improvements in successive sprints are likely to be dependent on improvements in aerobic metabolism as demonstrated by a greater increase in aerobic ATP provision as multiple-sprints exercise progresses (35). Therefore, although improvements in successive sprints may be dependent on improvements in aerobic metabolism as demonstrated by a greater increase in aerobic ATP provision as multiple-sprints exercise progresses (35), the extent of this is dependent on the program variables used, which may explain the greater increases in anaerobic measures.

Few studies have investigated the relative importance of intervention duration, training volume, and training frequency in mediating the magnitude and time course of physiological adaptations following SIT. The results of the current review identified a positive association between the pooled effect size and training volume (Table 4) quantified by the average number of sprints performed per session. This finding contradicts a previous meta-analysis conducted by Vollaard et al. (109) who did not find a clear relationship between the number of sprints performed in each session and change in V̇o2max, but estimated that the relationship was most likely to be negative with improvements maximized by performing only 2 sprints per session. The dose-response relationship to SIT is likely to be determined by complex interactions between several factors with multiple ways to accumulate higher training volumes that could influence outcomes. Previous research by Stavrinou et al. (98) identified that increasing training volume through increased frequency from 2 to 3 interval sessions per week resulted in greater increases in a range of outcome variables and altered the time course over which positive improvements were obtained. At present, there is limited research to summarize the relationship between improvements in SIT and training volume. Both the meta-regressions conducted in the present review and by Vollard et al. (109) were linear in nature. However, it is unlikely that the underlying relationship would be linear and consistent with other training modalities an initial positive relationship that plateaus and then reverses may be most likely.

The meta-regressions conduced in the current review also demonstrated increased effectiveness with long duration sprints (>20 seconds) compared with short duration sprints (<10 seconds) across all outcome categories (Table 4). Most outcomes (72%) included in the meta-analysis were extracted from 30-second sprints, reflecting seminal research conducted on Wingate-based protocols (10,38,63). However, based on criticisms that repeated 30-second sprints may not be time efficient overall (48,61), there has been an increasing number studies investigating shorter duration sprints. The finding that increased effect sizes may be obtained with longer-duration sprints is consistent with previous research demonstrating greater oxidative contributions to ATP turnover because of PCr depletion and glycolytic inhibition (38), resulting in increased mitochondrial biogenesis, mitochondrial enzyme activity, and skeletal muscle capillarization (15). Additionally, during longer-duration sprints, the number of muscular contraction cycles (i.e., cross-bridge attachments and detachments) are increased leading to greater disturbances in metabolic environments, potentially augmenting the response. Although this mechanism is yet to be fully explored, increased cross-bridge cycling will promote greater movement of calcium ions (Ca2+), increased levels of adenosine monophosphate (AMP) and AMP-activated protein kinase activation, and subsequent rate of peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) expression (30,41,59,90,102). Following repeated 30-second sprints, PGC-1α expression has been shown to increase 7-fold (102) compared with only 2-fold following 4-second sprints (90), with associations demonstrated between PGC-1α expression and mitochondrial adaptations and improvements in physical performance (30,41,59). However, it is important to note that the aforementioned measures were taken 4 and 3 hours, respectively, following sprints, with measures taken from messenger RNA and not protein changes (90,102). Further research is required to identify the influence of sprint duration on adaptations to SIT interventions and the underling mechanisms that may be responsible.

The only meta-regressions to exhibit clearer difference in moderating effect across outcome types were obtained with work-to-rest ratios (Table 4). When analyzed across all outcomes the meta-regression identified no evidence of an effect. However, when split by outcome type, the results identified that work-to-rest ratios with shorter rest periods were more effective for aerobic outcomes, whereas ratios with longer rest periods were more effective for anaerobic outcomes. These findings are consistent with those reported by Kavaliauskas et al. (53) who investigated the effects of a SIT intervention comprising 10-second sprints interspersed with either a 30-, 80-, or 120-second recovery. The aerobic performance measures demonstrating greater improvements with shorter rest periods included V̇o2peak, incremental time to exhaustion, and 3-km time trial, whereas the anaerobic performance measures demonstrating greater improvements with longer rest periods included peak and mean power output (53). These adaptations were suggested to occur because of reduced rest periods eliciting a greater aerobic challenge from a lack of PCr replenishment and glycolytic inhibition and longer rest periods enabling greater PCr resynthesis and increased power output to stimulate anaerobic adaptations (53). This hypothesis is supported by a recent acute comparison study demonstrating a stronger cardiorespiratory response with higher VEpeak, V̇o2peak, and HRpeak values in subjects performing 10-second sprints interspersed with 30 seconds vs. 4 minutes of recovery periods (27). In contrast, no significant differences were reported by Lloyd Jones et al. (62) for groups performing 6-second sprints interspersed with 48, 60, or 72 seconds of recovery periods for either aerobic (10-km time trial) or anaerobic (peak power output, mean power output) performance measures. Similarly, Olek et al. (79) reported no significant differences in aerobic, anaerobic, or skeletal muscle enzyme activity following 2 weeks of 10 seconds SIT matched for total sprint time but with 2 different recovery times (1 vs. 4 minutes). Contrasting results between studies may be because of a range of factors, including the length of interventions, different work-to-rest ranges investigated across groups, and the interrelation between factors, such as sprint duration and the nature of the recovery (active vs. passive). The results from this meta-analysis and the subsequent increased statistical power obtained support the hypothesis that work-to-rest ratios can be altered to more effectively target aerobic- or anaerobic-based outcomes. However, the modifying effects reported must be treated with caution as aggregate analyses made over studies may not hold at the individual level. In addition to statistical heterogeneity because of compounding intervention differences (e.g., types of subjects, training stimulus, and setting), methodological differences (e.g., control over bias) can also act to confound moderator analyses.

Consistent with the findings reported by Vollard et al. (109), the current meta-analysis identified no moderating effects of sprint resistance. Clustering of loads may have influenced results with most studies (79%) applying resistance as a percentage of body mass and selecting a load of 7.5%. Given the consistent use of 7.5% body mass as a resistance, only 2 authors in the included studies that selected an alternative value provided justification. Broatch et al. (13) stated that the selection of an increased resistance was made to reduce power output to 20 W·s−1, whereas Kavaliauskas et al. (54) selected a reduced resistance for female subjects because of lower expected muscle mass compared with male subjects. Although scaling resistance to body mass is less challenging practically, scaling to muscle mass may represent a more standardized stimulus for training prescription and represents an area for future research.

In the current review, methodological quality of studies was assessed using a modified version of the Downs and Black checklist. Most studies were classified as moderate (51%) or low (42%) in methodological quality. The average score obtained was 62% with the highest scoring study achieving 88% (7,13) and the lowest 37% (46), which was the only study to be classified as very low. The most notable methodological limitations identified in the present review included failure to blind outcome assessors, a lack of statistical power, and limited reporting of familiarization sessions. Similar findings have been reported by Sultana et al. (101) who also used a modified Downs and Black checklist and Rosenblat et al. (86) who used the PEDro scale. Previous authors identified similar limitations and noted the substantive risk of bias in comparison studies where outcome assessors were not blinded to allocation. The methodological limitations identified in the present review may also have contributed to the finding of extensive funnel plot asymmetry. Often wrongly attributed solely to publication bias, funnel plot asymmetry can be caused by a range of phenomenon collectively referred to as small study effects (100). Statistical heterogeneity and methodological differences can be causes of small study effects if they induce correlations between sampling error and intervention effects. However, sample size across the included studies was consistent with the interquartile range restricted to between 8 and 11 subjects such that statistical heterogeneity may not be the most influential factor explaining the asymmetry. Previous meta-analyses investigating SIT interventions have not identified any small study effects. Funnel plots and associated null hypothesis tests were presented by Gist et al. (44), Vollaard et al. (109), and Rosenblat et al. (86) with authors reporting nonsignificant results and no clear asymmetry in the visual plots. Across these reviews, the number of data points investigated was low ranging from 9 to 38, reflecting the narrow focus of the reviews to either V̇o2max or V̇o2peak. In contrast, in the present meta-analysis, a total of 411 outcomes were included in the primary meta-analysis across an extensive range of variables reflecting many different physical outcomes relevant to sporting performance. The included studies featured interventions conducted on cycle ergometers popular within exercise science laboratories. Software packages connected to cycle ergometers automatically calculate numerous variables that can be analyzed and presented as absolute or relative values. Additionally, researchers often compare these variables across multiple repetitions and time points, thereby increasing the reported number of outcomes. Across the included studies in the present review, the median number of outcomes extracted was 7, with 15 or more outcomes extracted from more than 25% of the studies. Based on the performance focus of this review, additional variables such as metabolic markers and muscle fiber measures, which are also frequently reported in SIT intervention studies, were not included in this summary such that the actual number of variables analyzed by authors was even higher. The potential for researchers to retrospectively select among an extensive pool of variables and publish multiple outcomes is a common problem in sport and exercise science, which leads to overestimation of effects (20), and may be a primary factor creating the small study effects identified in the present review. With many variables and small subject numbers, by chance, effects for many variables will be overestimated, and in a relatively small number of cases, overestimations will be extremely large.

An additional source of bias that has the potential to overestimate effects reported in this current review is the lack of familiarization with testing procedures. Approximately half (53%) of the included studies integrated familiarization with testing protocols. Where this was included, it was mainly limited to just 1 familiarization session or minimal information was provided regarding the procedures adopted. Connected to the issue of familiarization, the present review identified that only 20% of the included studies reported the reliability of main outcome measures, further limiting the confidence that can be placed on accuracy. To assess the effects of potential sources of bias, a comparison between effect sizes calculated with and without nonexercise controls was included. The results identified a small positive bias with noncontrolled effect sizes; however, some data points demonstrated very large positive errors (Figure 4). Additionally, it may be expected that studies that include a control group are generally of a higher overall quality and are less likely to exhibit large systematic biases. Collectively, instances of very large differences between noncontrolled and controlled effect sizes, and the presence of many very large effect sizes (41 effects > 2), despite interventions generally lasting between 2 and 4 weeks, demonstrate that the small study effects identified present a challenge for accurately estimating the benefits of SIT interventions and the most important moderators to generate optimum protocols.

The findings from the present review suggest several important areas for future research. First, the review highlights that a large array of both performance outcomes and SIT protocols have been investigated, with the results generally demonstrating moderate improvements. Reflecting the moderator analyses conducted here, future research should continue to tease out combinations of protocols that maximize specific predetermined adaptations. However, greater emphasis is required on establishing effective methods to progress SIT training and obtain greater improvements over longer periods. Most studies investigating SIT interventions are extremely short in duration and often feature no variation or progression in the training stimulus. Where progression has been included, it has generally been restricted to small increases in the number of sprints performed per session. However, given the complexity and interrelated nature of SIT training variables, progression could be achieved through many different options. It is recommended that future studies focus on longer duration interventions guided by periodization structures and research designs investigated with other training modalities, such as resistance training. Second, the review highlights limitations of the evidence base that are consistent with other areas in sports science. Most notably, the review identified extensive small study effects that are suggested to be caused primarily by a posteriori selection of outcome variables and data reduction procedures. It is recommended that where possible, future research should be hypothesis driven with clear and defined outcome measures that best match the aims and hypothesis of the research. It is also recommended that studies select a priori a smaller number outcomes that demonstrate appropriate validity, reliability (only 20% of studies reported reliability of outcome measures), and practical relevance. To address issues of statistical power and precision of effect size estimates, it is suggested that more collaborative work featuring multicenter data collection be considered. Given the ability to standardize training protocols on cycle ergometers and the consistency of equipment used, SIT research may provide an effective model for prospective multicenter collaboration. With regards to improvement of overall methodological quality, prospective reference tools, such as the Downs and Black checklist, the Consolidated Standards of Reporting Trials (CONSORT), and Consensus on Exercise Reporting Template (CERT), can assist with study design and address common limitations, including use of small sample sizes, omission of control groups, and insufficient use of familiarization sessions (9,29,93).

Practical Applications

Short-term SIT interventions can be used to create medium improvements across a range of physical performance outcomes in healthy individuals.Training protocols comprising longer sprint durations and more sprints result in greater improvements in performance outcomes. These outcomes can be affected by the work-to-rest ratio, with shorter rest periods more effective for aerobic outcomes, whereas longer rest periods were more effective for anaerobic outcomes.Future SIT interventions studies should be designed and conducted in accordance with the proposed methodological guidelines identified within this review. It is recommended that before data collection, researchers select a limited number of outcomes that match the research hypothesis and select data reduction procedures that are appropriate and adequately statistical powered accounting for multiplicity issues. Use of research evaluation tools (Downs and Black, CONSORT & CERT) should be used to inform study design.

Acknowledgments

Summaries of data generated within the present study will be included within the published article and supplementary files. Further data requests should be made through reasonable contact with the corresponding author. The authors declare there are no conflicts of interest or competing interests. The protocol was designed by A. J. Hall, P. A. Swinton, and T. P. Craig; A. J. Hall, P. A. Swinton, and T. P. Craig independently undertook the searches and selected studies. A. J. Hall and T. P. Craig screened all titles and abstracts of sources and independently completed data extraction. Where discrepancies or disagreements occurred, with these were resolved through collective agreements with P. A. Swinton, M. Kavaliauskas, and R. R. Aspe. Methodological quality and risk of bias were evaluated by T. P. Craig, R. R. Aspe, and M. Kavaliauskas; P. A. Swinton undertook all statistical analyses, with the resultant manuscript written by A. J. Hall, P. A. Swinton, R. R. Aspe, M. Kavaliauskas, and J. Babraj. All authors have read and approved the final manuscript.

References

1. Akca F, Aras D. Comparison of rowing performance improvements following various high-intensity interval trainings. J Strength Cond Res 29: 2249–2254, 2015.
2. Astorino TA, Allen RP, Roberson DW, et al. Adaptations to high-intensity training are independent of gender. Eur J Appl Physiol 111: 1279–1286, 2011.
3. Babraj JA, Vollaard NB, Keast C, et al. Extremely short duration high intensity interval training substantially improves insulin action in young healthy males. BMC Endocr Disord 9: 9, 2009.
4. Bailey SJ, Wilkerson DP, DiMenna FJ, Jones AM. Influence of repeated sprint training on pulmonary O2 uptake and muscle deoxygenation kinetics in humans. J Appl Physiol (1985) 106: 1875–1887, 2009.
5. Barnett C, Carey M, Proietto J, et al. Muscle metabolism during sprint exercise in man: Influence of sprint training. J Sci Med Sport 7: 314–322, 2004.
6. Bayati M, Farzad B, Gharakhanlou R, Agha-Alinejad H. A practical model of low-volume high-intensity interval training induces performance and metabolic adaptations that resemble ‘all-out’ sprint interval training. J Sports Sci Med 10: 571–576, 2011.
7. Benítez-Flores S, Medeiros AR, Voltarelli FA, et al. Combined effects of very short “all out” efforts during sprint and resistance training on physical and physiological adaptations after 2 weeks of training. Eur J Appl Physiol 119: 1337–1351, 2019.
8. Billat LV. Interval training for performance: A scientific and empirical practice. Sports Med 31: 13–31, 2001.
9. Bishop D. An applied research model for the sport sciences. Sports Med 38: 253–263, 2008.
10. Bogdanis GC, Nevill ME, Boobis LH, Lakomy HK, Nevill AM. Recovery of power output and muscle metabolites following 30 s of maximal sprint cycling in man. J Physiol 482(Pt 2): 467–480, 1995.
11. Bogdanis GC, Nevill ME, Boobis LH, Lakomy HK. Contribution of phosphocreatine and aerobic metabolism to energy supply during repeated sprint exercise. J Appl Physiol (1985) 80: 876–884, 1996.
12. Bogdanis GC, Nevill ME, Lakomy HK, Boobis LH. Power output and muscle metabolism during and following recovery from 10 and 20 s of maximal sprint exercise in humans. Acta Physiol Scand 163: 261–272, 1998.
13. Broatch JR, Petersen A, Bishop DJ. Cold-water immersion following sprint interval training does not alter endurance signaling pathways or training adaptations in human skeletal muscle. Am J Physiol Regul Integr Comp Physiol 313: R372–R384, 2017.
14. Buchheit M, Laursen PB. High-intensity interval training, solutions to the programming puzzle. Sports Med 43: 927–954, 2013.
15. Burgomaster KA, Hughes SC, Heigenhauser GJ, Bradwell SN, Gibala MJ. Six sessions of sprint interval training increases muscle oxidative potential and cycle endurance capacity in humans. J Appl Physiol (1985) 98: 1985–1990, 2005.
16. Burgomaster KA, Heigenhauser GJ, Gibala MJ. Effect of short-term sprint interval training on human skeletal muscle carbohydrate metabolism during exercise and time-trial performance. J Appl Physiol (1985) 100: 2041–2047, 2006.
17. Burgomaster KA, Cermak NM, Phillips SM, et al. Divergent response of metabolite transport proteins in human skeletal muscle after sprint interval training and detraining. Am J Physiol Regul Integr Comp Physiol 292: R1970–R1976, 2007.
18. Burgomaster KA, Howarth KR, Phillips SM, et al. Similar metabolic adaptations during exercise after low volume sprint interval and traditional endurance training in humans. J Physiol 586: 151–160, 2008.
19. Bürkner P. An R package for bayesian multilevel models using stan. J Statist Softw 80: 1–28, 2017.
20. Buttner F, Toomey E, McClean S, Roe M, Delahunt E. Are questionable research practices facilitating new discoveries in sport and exercise medicine? The proportion of supported hypotheses is implausibly high. Br J Sports Med 54: 1365–1371, 2020.
21. Caldwell A, Vigotsky AD. A case against default effect sizes in sport and exercise science. PeerJ 8: e10314, 2020.
22. Camacho-Cardenosa M, Camacho-Cardenosa A, Martinez Guardado I, et al. A new dose of maximal-intensity interval training in hypoxia to improve body composition and hemoglobin and hematocrit levels: A pilot study. J Sports Med Phys Fitness 57: 60–69, 2017.
23. Cochran AJR, Percival ME, Thompson S, et al. Beta-alanine supplementation does not augment the skeletal muscle adaptive response to 6 weeks of sprint interval training. Int J Sport Nutr Exerc Metab 25: 541–549, 2015.
24. Cocks M, Shaw CS, Shepherd SO, et al. Sprint interval and endurance training are equally effective in increasing muscle microvascular density and eNOS content in sedentary males. J Physiol 591: 641–656, 2013.
25. Cohen J. Statistical Power Analysis for the Behavioral Sciences. New York, NY: Academic press, 2013.
26. Creer AR, Ricard MD, Conlee RK, Hoyt GL, Parcell AC. Neural, metabolic, and performance adaptations to four weeks of high intensity sprint-interval training in trained cyclists. Int J Sports Med 25: 92–98, 2004.
27. Danek N, Smolarek M, Michalik K, Zatoń M. Comparison of acute responses to two different cycling sprint interval exercise protocols with different recovery durations. Int J Environ Res Public Health 17: 1026, 2020.
28. Downs SH, Black N. The feasibility of creating a checklist for the assessment of the methodological quality both of randomised and non-randomised studies of health care interventions. J Epidemiol Commun Health 52: 377–384, 1998.
29. Dwan K, Li T, Altman DG, Elbourne D. CONSORT 2010 statement: Extension to randomised crossover trials. BMJ 366: l4378, 2019.
30. Edgett BA, Bonafiglia JT, Baechler BL, Quadrilatero J, Gurd BJ. The effect of acute and chronic sprint-interval training on LRP130, SIRT3, and PGC-1alpha expression in human skeletal muscle. Physiol Rep 4: e12879, 2016.
31. Esfarjani F, Laursen PB. Manipulating high-intensity interval training: Effects on VO2max, the lactate threshold and 3000 m running performance in moderately trained males. J Sci Med Sport 10: 27–35, 2007.
32. Estrada E, Ferrer E, Pardo A. Statistics for evaluating pre-post change: Relation between change in the distribution center and change in the individual scores. Front Psychol 9: 2696, 2019.
33. Etxebarria N, Anson JM, Pyne DB, Ferguson RA. High-intensity cycle interval training improves cycling and running performance in triathletes. Eur J Sport Sci 14: 521–529, 2014.
34. Fernández-Castilla B, Declercq L, Jamshidi L, et al. Detecting selection bias in meta-analyses with multiple outcomes: A simulation study. J Exp Educ 89: 1–20, 2019.
35. Fiorenza M, Hostrup M, Gunnarsson TP, et al. Neuromuscular fatigue and metabolism during high-intensity intermittent exercise. Med Sci Sports Exerc 51: 1642–1652, 2019.
36. Forbes SC, Slade JM, Meyer RA. Short-term high-intensity interval training improves phosphocreatine recovery kinetics following moderate-intensity exercise in humans. Appl Physiol Nutr Metab 33: 1124–1131, 2008.
37. Fu R, Gartlehner G, Grant M, et al. Conducting quantitative synthesis when comparing medical interventions: AHRQ and the effective health care program. J Clin Epidemiol 64: 1187–1197, 2011.
38. Gaitanos GC, Williams C, Boobis LH, Brooks S. Human muscle metabolism during intermittent maximal exercise. J Appl Physiol (1985) 75: 712–719, 1993.
39. Gelman A, Carlin JB, Stern HS, et al. Bayesian Data Analysis. London: CRC press, 2013.
40. Gibala MJ, Little JP, van Essen M, et al. Short-term sprint interval versus traditional endurance training: Similar initial adaptations in human skeletal muscle and exercise performance. J Physiol 575: 901–911, 2006.
41. Gibala MJ, McGee SL, Garnham AP, et al. Brief intense interval exercise activates AMPK and p38 MAPK signaling and increases the expression of PGC-1α in human skeletal muscle. J Appl Physiol 106: 929–934, 2009.
42. Gibala MJ, Little JP, Macdonald MJ, Hawley JA. Physiological adaptations to low-volume, high-intensity interval training in health and disease. J Physiol 590: 1077–1084, 2012.
43. Gillen JB, Martin BJ, MacInnis MJ, et al. Twelve weeks of sprint interval training improves indices of cardiometabolic health similar to traditional endurance training despite a five-fold lower exercise volume and time commitment. PLoS One 11: e0154075, 2016.
44. Gist NH, Fedewa MV, Dishman RK, Cureton KJ. Sprint interval training effects on aerobic capacity: A systematic review and meta-analysis. Sports Med 44: 269–279, 2014.
45. Guyatt GH, Oxman AD, Vist GE, et al. GRADE: An emerging consensus on rating quality of evidence and strength of recommendations. BMJ 336: 924–926, 2008.
46. Harmer AR, McKenna MJ, Sutton JR, et al. Skeletal muscle metabolic and ionic adaptations during intense exercise following sprint training in humans. J Appl Physiol (1985) 89: 1793–1803, 2000.
47. Harris E, Rakobowchuk M, Birch KM. Sprint interval and sprint continuous training increases circulating CD34+ cells and cardio-respiratory fitness in young healthy women. PLoS One 9: e108720, 2014.
48. Hazell TJ, MacPherson RE, Gravelle BM, Lemon PW. 10 or 30-s sprint interval training bouts enhance both aerobic and anaerobic performance. Eur J Appl Physiol 110: 153–160, 2010.
49. Hommel J, Öhmichen S, Rudolph UM, Hauser T, Schulz H. Effects of six-week sprint interval or endurance training on calculated power in maximal lactate steady state. Biol Sport 36: 47–54, 2019.
50. Ijichi T, Hasegawa Y, Morishima T, et al. Effect of sprint training: Training once daily versus twice every second day. Eur J Sport Sci 15: 143–150, 2015.
51. Ikutomo A, Kasai N, Goto K. Impact of inserted long rest periods during repeated sprint exercise on performance adaptation. Eur J Sport Sci 18: 47–53, 2018.
52. Jakeman J, Adamson S, Babraj J. Extremely short duration high-intensity training substantially improves endurance performance in triathletes. Appl Physiol Nutr Metab 37: 976–981, 2012.
53. Kavaliauskas M, Aspe RR, Babraj J. High-intensity cycling training: The effect of work-to-rest intervals on running performance measures. J Strength Cond Res 29: 2229–2236, 2015.
54. Kavaliauskas M, Steer TP, Babraj JA. Cardiorespiratory fitness and aerobic performance adaptations to a 4-week sprint interval training in young healthy untrained females. Sport Sci Health 13: 17–23, 2017.
55. Kruschke JK, Liddell TM. The Bayesian new statistics: Hypothesis testing, estimation, meta-analysis, and power analysis from a Bayesian perspective. Psychon Bull Rev 25: 178–206, 2018.
56. Larsen RG, Maynard L, Kent JA. High-intensity interval training alters ATP pathway flux during maximal muscle contractions in humans. Acta Physiol (Oxf) 211: 147–160, 2014.
57. Lewis EJH, Stucky F, Radonic PW, et al. Neuromuscular adaptations to sprint interval training and the effect of mammalian omega-3 fatty acid supplementation. Eur J Appl Physiol 117: 469–482, 2017.
58. Linossier MT, Dormois D, Perier C, et al. Enzyme adaptations of human skeletal muscle during bicycle short‐sprint training and detraining. Acta Physiol Scand 161: 439–445, 1997.
59. Little JP, Safdar A, Bishop D, Tarnopolsky MA, Gibala MJ. An acute bout of high-intensity interval training increases the nuclear abundance of PGC-1α and activates mitochondrial biogenesis in human skeletal muscle. Am J Physiol Regul Integr Comp Physiol 300: R1303–R1310, 2011.
60. Little JP, Langley J, Lee M, et al. Sprint exercise snacks: A novel approach to increase aerobic fitness. Eur J Appl Physiol 119: 1203–1212, 2019.
61. Lloyd Jones MC, Morris MG, Jakeman JR. Impact of time and work:rest ratio matched sprint interval training programmes on performance: A randomised controlled trial. J Sci Med Sport 20: 1034–1038, 2017.
62. Lloyd Jones MC, Morris MG, Jakeman JR. Effect of work: Rest ratio on cycling performance following sprint interval training: A randomized control trial. J Strength Cond Res 33: 3263–3268, 2019.
63. MacDougall JD, Hicks AL, MacDonald JR, et al. Muscle performance and enzymatic adaptations to sprint interval training. J Appl Physiol (1985) 84: 2138–2142, 1998.
64. McGarr GW, Hartley GL, Cheung SS. Neither short-term sprint nor endurance training enhances thermal response to exercise in a hot environment. J Occup Environ Hyg 11: 47–53, 2014.
65. Metcalfe RS, Babraj JA, Fawkner SG, Vollaard NB. Towards the minimal amount of exercise for improving metabolic health: Beneficial effects of reduced-exertion high-intensity interval training. Eur J Appl Physiol 112: 2767–2775, 2012.
66. Metcalfe R, Fawkner S, Vollaard N. No acute effect of reduced-exertion high-intensity interval training (REHIT) on insulin sensitivity. Int J Sports Med 37: 354–358, 2016.
67. Metcalfe RS, Tardif N, Thompson D, Vollaard NB. Changes in aerobic capacity and glycaemic control in response to reduced-exertion high-intensity interval training (REHIT) are not different between sedentary men and women. Appl Physiol Nutr Metab 41: 1117–1123, 2016.
68. Milanović Z, Sporiš G, Weston M. Effectiveness of high-intensity interval training (HIT) and continuous endurance training for VO improvements: A systematic review and meta-analysis of controlled trials. Sports Med 45: 1469–1481, 2015.
69. Mitchell BL, Lock MJ, Davison K, et al. What is the effect of aerobic exercise intensity on cardiorespiratory fitness in those undergoing cardiac rehabilitation? A systematic review with meta-analysis. Br J Sports Med 53: 1341–1351, 2019.
70. Moher D, Liberati A, Tetzlaff J, Altman DG, Prisma Group. Preferred reporting items for systematic reviews and meta-analyses: The PRISMA statement. BMJ 339: b2535, 2009.
71. Moreno SG, Sutton AJ, Ades AE, et al. Assessment of regression-based methods to adjust for publication bias through a comprehensive simulation study. BMC Med Res Methodol 12: 9, 2009.
72. Morris SB. Estimating effect sizes from pretest-posttest-control group designs. Organ Res Methods 11: 364–386, 2008.
73. Muggeridge DJ, Sculthorpe N, James PE, Easton C. The effects of dietary nitrate supplementation on the adaptations to sprint interval training in previously untrained males. J Sci Med Sport 20: 92–97, 2017.
74. Naimo MA, de Souza EO, Wilson JM, et al. High-intensity interval training has positive effects on performance in ice hockey players. Int J Sports Med 36: 61–66, 2015.
75. Nalçakan GR, Songsorn P, Fitzpatrick BL, et al. Decreasing sprint duration from 20 to 10 s during reduced-exertion high-intensity interval training (REHIT) attenuates the increase in maximal aerobic capacity but has no effect on affective and perceptual responses. Appl Physiol Nutr Metab 43: 338–344, 2018.
76. Nalçakan GR. The effects of sprint interval vs. continuous endurance training on physiological and metabolic adaptations in young healthy adults. J Hum Kinet 44: 97–109, 2014.
77. Naves JPA, Viana RB, Rebelo ACS, et al. Effects of high-intensity interval training vs. sprint interval training on anthropometric measures and cardiorespiratory fitness in healthy young women. Front Physiol 9: 2018.
78. O'Driscoll JM, Wright SM, Taylor KA, et al. Cardiac autonomic and left ventricular mechanics following high intensity interval training: A randomized crossover controlled study. J Appl Physiol (1985) 125: 1030–1040, 2018.
79. Olek RA, Kujach S, Ziemann E, et al. Adaptive changes after 2 weeks of 10-s sprint interval training with various recovery times. Front Physiol 9: 1738, 2018.
80. Ørtenblad N, Lunde PK, Levin K, Andersen JL, Pedersen PK. Enhanced sarcoplasmic reticulum ca(2+) release following intermittent sprint training. Am J Physiol Regul Integr Comp Physiol 279: R152–R160, 2000.
81. Parra J, Cadefau JA, Rodas G, Amigó N, Cussó R. The distribution of rest periods affects performance and adaptations of energy metabolism induced by high-intensity training in human muscle. Acta Physiol Scand 169: 157–165, 2000.
82. Rakobowchuk M, Tanguay S, Burgomaster KA, et al. Sprint interval and traditional endurance training induce similar improvements in peripheral arterial stiffness and flow-mediated dilation in healthy humans. Am J Physiol Regul Integr Comp Physiol 295: R236–R242, 2008.
83. Ramos JS, Dalleck LC, Tjonna AE, Beetham KS, Coombes JS. The impact of high-intensity interval training versus moderate-intensity continuous training on vascular function: A systematic review and meta-analysis. Sports Med 45: 679–692, 2015.
84. Richardson AJ, Gibson OR. Simulated hypoxia does not further improve aerobic capacity during sprint interval training. J Sports Med Phys Fitness 55: 1099–1106, 2015.
85. Rodas G, Ventura JL, Cadefau JA, Cussó R, Parra J. A short training programme for the rapid improvement of both aerobic and anaerobic metabolism. Eur J Appl Physiol 82: 480–486, 2000.
86. Rosenblat MA, Perrotta AS, Thomas SG. Effect of high-intensity interval training versus sprint interval training on time-trial performance: A systematic review and meta-analysis. Sports Med 50: 1–17, 2020.
87. Saunders B, Elliott-Sale K, Artioli GG, et al. Beta-alanine supplementation to improve exercise capacity and performance: A systematic review and meta-analysis. Br J Sports Med 51: 658–669, 2017.
88. Scalzo RL, Peltonen GL, Binns SE, et al. Greater muscle protein synthesis and mitochondrial biogenesis in males compared with females during sprint interval training. FASEB J 28: 2705–2714, 2014.
89. Schlittler M, Neyroud D, Tanga C, et al. Three weeks of sprint interval training improved high-intensity cycling performance and limited ryanodine receptor modifications in recreationally active human subjects. Eur J Appl Physiol 119: 1951–1958, 2019.
90. Serpiello FR, McKenna MJ, Bishop DJ, et al. Repeated sprints alter signaling related to mitochondrial biogenesis in humans. Med Sci Sports Exerc 44: 827–834, 2012.
91. Shenouda N, Gillen JB, Gibala MJ, MacDonald MJ. Changes in brachial artery endothelial function and resting diameter with moderate-intensity continuous but not sprint interval training in sedentary men. J Appl Physiol (1985) 123: 773–780, 2017.
92. Shepherd SO, Cocks M, Tipton KD, et al. Sprint interval and traditional endurance training increase net intramuscular triglyceride breakdown and expression of perilipin 2 and 5. J Physiol 591: 657–675, 2013.
93. Slade SC, Dionne CE, Underwood M, Buchbinder R. Consensus on exercise reporting template (CERT): Explanation and elaboration statement. Br J Sports Med 50: 1428–1437, 2016.
94. Sloth M, Sloth D, Overgaard K, Dalgas U. Effects of sprint interval training on VO2max and aerobic exercise performance: A systematic review and meta-analysis. Scand J Med Sci Sports 23: e341–e352, 2013.
95. Songsorn P, Lambeth-Mansell A, Mair JL, et al. Exercise training comprising of single 20-s cycle sprints does not provide a sufficient stimulus for improving maximal aerobic capacity in sedentary individuals. Eur J Appl Physiol 116: 1511–1517, 2016.
96. Sousa FAB, Vasque RE, Gobatto CA. Anaerobic metabolism during short all-out efforts in tethered running: Comparison of energy expenditure and mechanical parameters between different sprint durations for testing. PLoS One 12: e0179378, 2017.
97. Sousa AC, Fernandes RJ, Boas JPV, Figueiredo P. High-intensity interval training in different exercise modes: Lessons from time to exhaustion. Int J Sports Med 39: 668–673, 2018.
98. Stavrinou PS, Bogdanis GC, Giannaki CD, Terzis G, Hadjicharalambous M. High-intensity interval training frequency: Cardiometabolic effects and quality of life. Int J Sports Med 39: 210–217, 2018.
99. Stepto NK, Hawley JA, Dennis SC, Hopkins WG. Effects of different interval-training programs on cycling time-trial performance. Med Sci Sports Exerc 31: 736–741, 1999.
100. Sterne JA, Sutton AJ, Ioannidis JP, et al. Recommendations for examining and interpreting funnel plot asymmetry in meta-analyses of randomised controlled trials. BMJ 343: d4002, 2011.
101. Sultana RN, Sabag A, Keating SE, Johnson NA. The effect of low-volume high-intensity interval training on body composition and cardiorespiratory fitness: A systematic review and meta-analysis. Sports Med 49: 1–35, 2019.
102. Taylor CW, Ingham SA, Hunt JE, et al. Exercise duration-matched interval and continuous sprint cycling induce similar increases in AMPK phosphorylation, PGC-1α and VEGF mRNA expression in trained individuals. Eur J Appl Physiol 116: 1445–1454, 2016.
103. Terada T, Toghi Eshghi SR, Liubaoerjijin Y, et al. Overnight fasting compromises exercise intensity and volume during sprint interval training but improves high-intensity aerobic endurance. J Sports Med Phys Fitness 59: 357–365, 2019.
104. Thompson C, Wylie LJ, Blackwell JR, et al. Influence of dietary nitrate supplementation on physiological and muscle metabolic adaptations to sprint interval training. J Appl Physiol (1985) 122: 642–652, 2017.
105. Thompson C, Vanhatalo A, Kadach S, et al. Discrete physiological effects of beetroot juice and potassium nitrate supplementation following 4-wk sprint interval training. J Appl Physiol (1985) 124: 1519–1528, 2018.
106. Vera-Ibanez A, Colomer-Poveda D, Romero-Arenas S, Vinuela-Garcia M, Marquez G. Neural adaptations after short-term wingate-based high-intensity interval training. J Musculoskelet Neuronal Interact 17: 275–282, 2017.
107. Viana RB, de Lira C, Barbosa A, et al. Can we draw general conclusions from interval training studies? Sports Med 48: 2001–2009, 2018.
108. Viana AA, Fernandes B, Alvarez C, Guimarães GV, Ciolac EG. Prescribing high-intensity interval exercise by RPE in individuals with type 2 diabetes: Metabolic and hemodynamic responses. Appl Physiol Nutr Metab 44: 348–356, 2019.
109. Vollaard NBJ, Metcalfe RS, Williams S. Effect of number of sprints in an SIT session on change in VO2max: A meta-analysis. Med Sci Sports Exerc 49: 1147–1156, 2017.
110. Weston KS, Wisløff U, Coombes JS. High-intensity interval training in patients with lifestyle-induced cardiometabolic disease: A systematic review and meta-analysis. Br J Sports Med 48: 1227–1234, 2014.
111. Yamagishi T, Babraj J. Effects of reduced-volume of sprint interval training and the time course of physiological and performance adaptations. Scand J Med Sci Sports 27: 1662–1672, 2017.
112. Yamagishi T, Babraj J. Active recovery induces greater endurance adaptations when performing sprint interval training. J Strength Cond Res 33: 922–930, 2019.
113. Zelt JG, Hankinson PB, Foster WS, et al. Reducing the volume of sprint interval training does not diminish maximal and submaximal performance gains in healthy men. Eur J Appl Physiol 114: 2427–2436, 2014.
Keywords:

SIT; high-intensity interval training; methodological quality; aerobic training; anaerobic training

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