Evidence of Disturbed Sleep and Increased Illness in Overreached Endurance Athletes : Medicine & Science in Sports & Exercise

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Evidence of Disturbed Sleep and Increased Illness in Overreached Endurance Athletes


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Medicine & Science in Sports & Exercise: May 2014 - Volume 46 - Issue 5 - p 1036-1045
doi: 10.1249/MSS.0000000000000177
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Increases in training intensity or volume are typically undertaken by athletes in an attempt to enhance physiological adaptation and to improve physical performance. However, when the balance between appropriate training stress and adequate recovery is disrupted, an abnormal training response may occur and a state of short-term “overreaching” (functional OR, F-OR) (21) may develop, resulting in a decline in performance. Although the F-OR state is generally reversed when an appropriate period of recovery is provided (∼1–3 wk) (16,21), it can compromise competition outcomes in the short term, particularly when insufficient recovery is available before competition. However, critical reviews of existing scientific literature continue to conclude that the underlying causes of F-OR in endurance athletes remain uncertain (10,21,24,36).

One of the most commonly reported methods for managing fatigue and enhancing recovery is obtaining adequate passive rest and sufficient sleep (23,30). The restorative qualities of sleep for maintaining optimal bodily function are well recognized. The recovery of cognitive processes and metabolic functions, both of which are important contributors to exercise performance, can be affected by the quality and quantity of sleep (30). Despite health-based survey research reporting associations between regular moderate physical activity and better sleep (4), few studies have reported alterations in sleep quality in response to highly demanding training programs (17,35). Taylor et al. (35) measured sleep via polysomnography during the “onset of training,” “heavy training,” and “precompetition taper” in elite female swimmers. Sleep onset latency, time awake after sleep onset, total sleep time, rapid eye movement, and sleep times were similar at all three training phases, but the number of movements during sleep was significantly higher (6%) during higher training volumes, suggesting some alteration to sleep. Nevertheless, the improvement in performance time and the low levels of tension and anger at peak training suggest that the swimmers were not F-OR. Recently, Fietze et al. (6) used wrist actigraphy during a 67-d period of high physical and mental stress to study sleep patterns in 24 classical ballet dancers before a ballet premiere performance. They found small but significant reduction in sleep duration (−6%), sleep efficiency (−2%), and time in bed (−3%) and an increase in wakefulness after sleep onset (+3%). Sleep onset latency did not change. Nevertheless, these authors did not report changes in physical performance in response to the prescribed overload program, making clear conclusions for sleep disruption in OR athletes difficult. However, studies during which sleep was monitored in athletes who demonstrated clear signs of OR (i.e., high perceived fatigue and decreased performance) remain few and involve self-reporting of reduced perceived subjective sleep quality (11,12). Given such equivocal findings, a recent joint consensus statement led Meeusen et al. (21) to recommend additional research to determine the relationship between F-OR and altered sleep patterns.

Past research showed that aspects of both innate and adaptive immunity are depressed during sustained periods of heavy training (for a review, see Walsh et al. [38]). An imbalance between training loads and recovery has been shown as a major contributor to illness (38). These abnormalities share similarities with impairment in immune function observed after moderate sleep deprivation (33). Vgontzas et al. (37) studied the effects of modest sleep restriction from 8 to 6 h per night for 1 wk in 25 young, healthy, normal sleepers for 12 consecutive nights in a sleep laboratory. Their results showed that modest sleep loss is associated with the significant increased secretion of proinflammatory cytokines, suggesting a link between the recuperative processes of sleep and the immune system. Similarly, Cohen et al. (3) showed that insufficient sleep volume over consecutive days can impair immune function and increase the risk of developing upper respiratory tract infections (URTI). These authors reported that participants with less than 7 h of sleep were 2.94 times more likely to develop a “cold” than those with 8 h or more of sleep once administered nasal drops containing a rhinovirus and monitored for ensuing development of a clinical cold. The association with sleep efficiency was also graded, with participants reporting <92% sleep efficiency 5.5 times more likely to develop a cold than those with >98% efficiency. Taken together, these results have led some authors to suggest that the potential immunosuppressive effects of overreaching may act through sleep disturbances (38). However, no scientific investigation to date provides evidence of this relationship to substantiate this argument.

The aim of the present study was therefore to determine whether changes in objective sleep parameters were evident between an experimental group of triathletes developing F-OR compared with a control group. After 1 wk of low volume training (baseline), the experimental group completed a 3-wk overload period followed by a 2-wk taper. By programming intensified training over a large population of endurance athletes (n = 28), we hypothesized that some participants would demonstrated signs of F-OR (i.e., transient reduced performance). By this way, the present research gave us also the opportunity to determine whether sleep disturbances would be observed during an overload period in participants led to F-OR. In the light of past literature, we hypothesized that the development of F-OR would be accompanied by a decline in sleep quality and sleep quantity. Furthermore, we investigated whether the potential presence of F-OR and reduced sleep quality in F-OR athletes would be accompanied with a higher prevalence of URTI.



Forty well-trained triathletes volunteered to participate in this study. All subjects had been competing for 3 yr and were training a minimum of 7 times per week. During the experimental period, seven subjects did not follow the protocol because of injury or personal obligations and were excluded from subsequent analyses. In addition, six participants, who worked at night with irregular schedules, were excluded from subsequent analyses. One subject was also excluded because of technical problems with equipment. The final sample size included in analysis was n = 27. The experimental design of the study was approved by the ethical committee of Saint-Germain-en-Laye (acceptance no. 12048) and was conducted in accordance with the Declaration of Helsinki. Before participation, subjects underwent medical assessment with a cardiologist to ensure normal electrocardiograph patterns and to obtain a general medical clearance. All subjects were free from chronic diseases and were not taking prescribed medication at the commencement of the study. After comprehensive verbal and written explanations of the study, all subjects gave their written informed consent to participate.

Study design

An overview of the study design is shown in Figure 1. The subjects were randomly assigned to either the control group (n = 9) or the overload training group (n = 18) according to a matched group experimental design based on maximal aerobic power (MAP), habitual training volume, and years of experience in endurance sports. All subjects had regularly competed in triathlons for at least 3 yr and were training a minimum of 10 h·wk−1. The training of each triathlete was monitored for a period of 9 wk in total, which was divided into a pretesting phase and then three distinct experimental phases. Both the pretesting phase and the first phase were the same for all groups. The pretesting phase consisted of 3 wk during which the subjects completed their usual training regime without any study intervention (i.e., normal training load). The first experimental phase (baseline) consisted of 1 wk of moderate training load during which the subjects were asked to reduce their habitual training volume by ∼50% while maintaining the training intensity. This minitaper was selected according to the guidelines for optimal tapering in endurance sports (2). During the second experimental period (overloading phase), the overload group completed a 3-wk overload program designed to deliberately overreach the subjects. The duration of each training session of the normal (pretesting) training period was increased by 30% (e.g., a 1-h run including eight repetitions of 400 m at the maximal aerobic running speed was converted into an 80-min run including 11 repetitions of 400 m at the maximal aerobic running speed). As particular subjects were unable to accommodate such prolonged-duration cycling sessions (≥5 h) into their routines, these specific sessions were split (e.g., a 5-h cycling session was converted into two sessions of 2h30). The participants reproduced the same training program during each week of the overload period so that both the content and the weekly distribution of the training sessions remained consistent. The control group repeated its habitual training program during this period. Next, all the participants completed a 2-wk taper period (third experimental phase, Taper), where their normal training load was decreased by 50% each week (e.g., a 1-h run including eight repetitions of 400 m at the maximal aerobic running speed was converted into a ∼30 min run including four repetitions of 400 m at the maximal aerobic running speed). All training sessions were performed by the triathletes in their own training structure according to the training program established by the same sport scientist. Throughout the entire study, the same sport scientist was responsible for coaching and controlling the training loads of all subjects. To avoid injuries, particular attention was devoted to daily feedback obtained from the triathletes. Before the beginning of the experimental period, the subject reported once to the laboratory to become familiarized with the maximal incremental cycling test (described in the next section) and the daily testing used during the protocol (sleep monitoring and questionnaires). Testing was performed on three occasions (Fig. 1), including Pre (i.e., after baseline phase), Mid (after overload phase), and Post (after taper phase), respectively. To ensure that performance variations during the maximal incremental cycling tests were due to the training regimen and not to the training session(s) performed the day before each test, the subjects respected a 24-h rest period before each laboratory session.

Schematic representation of the experimental protocol. Bicycle symbols represent maximal incremental cycling tests. Note that nine subjects of the overload group developed symptoms of functional overreaching at Mid (decreased performance vs preassociated with high perceived fatigue, F-OR group). The nine other overloaded subjects were only the AF group.

Training monitoring

Training volume and intensity were calculated and controlled on the basis of HR measurement (Polar, Kempele, Finland). For all subjects, HR was measured every 5 s during each training session over the entire protocol. The distribution of HR into training zones was subsequently calculated using three HR zones: 1) ≤ HR at 2 mmol·L−1, 2) between HR at 2 mmol·L−1 and HR at lactate threshold, and 3) HR values superior to HR at lactate threshold (for the description of the lactate threshold determination method, see Laboratory Testing section). Given that the relationship between blood lactate accumulation and HR values at exercise can be influenced by a heavy training load program (15), these reference HR values were reassessed after each maximal incremental cycling test.

Laboratory testing

During the 48 h before each maximal incremental cycling test, the subjects received specific nutritional guidelines to ensure muscle glycogen stores were replenish. Specifically, they were instructed to eat until satiety was reached during each lunch. Breakfast consisted of a variety of macronutrients from both solid and liquid energy sources. The selected foods included an assortment of cereals, bread, fruit, yogurt, milk, juice, ham, and cheese. For lunch and dinner, the subjects consumed a mixed salad as starter, then white meat during lunch and fish during dinner. The side plate consisted of a mixed of 50% carbohydrates (i.e., pasta, nice, and noodles) and 50% of vegetables (i.e., green beans, broccoli, and tomatoes). One piece of fruit and tub of yogurt were added as dessert, at both lunch and dinner. To ensure the subjects were well hydrated on each testing day, they were instructed to ensure the maintenance of a well-hydrated state.


Before exercise testing, subjects were asked to complete the POMS questionnaire to assess overall mood disturbance (19). The POMS questionnaire is a 65-item Likert scale questionnaire, which provides measures of six specific mood states: vigor, depression, fatigue, anger, anxiety, and confusion.

Performance and V˙O2max

Maximum oxygen uptake (V˙O2max) was assessed on an electronically braked cycle ergometer (Excalibur Sport; Lode®, Groningen, The Netherlands) equipped with standard 170-mm cranks, and the athletes used their own shoes. Positions of the handlebars and seat height were adjusted to the measures used by the athletes on their own bike and replicated between sessions. The test was performed until complete exhaustion to estimate V˙O2max and MAP. This exercise protocol started with a warm-up of 5 min at a workload of 100 W, followed by 5 min at 150 W and 5 min at 200 W. Thereafter, further increments of 25 W were added every 2 min until volitional exhaustion. Subjects wore a mask covering their mouth and nose for breath collection (Hans Rudolph, Kansas City, MO), and oxygen and carbon dioxide concentration in the expired gas was continuously measured and monitored as breath-by-breath values (Quark; Cosmed®, Rome, Italy). The gas analyzers and the flowmeter of the applied spirometer were calibrated before each test.

After the test, breath-by-breath values were visually inspected and averaged for 30 s. The highest 30-s average value was used as V˙O2max. MAP was calculated as MAP = Wcompl + 25(t/120), where Wcompl is the last completed workload and t is the number of seconds in Wcompl. In addition, the intensities and associated HR at which [La]b increased higher than 2 mmol·L−1 and the lactate threshold (LT) calculated by the modified D-max method (1) were subsequently determined.

Sleep monitoring

All subjects were monitored continuously using an Actiwatch worn on the nondominant wrist (Cambridge Neurotechnology Ltd., Cambridge, UK), with the epoch length set to 1 min. Athletes were monitored in the home environment every day at baseline (7 d), during overloading (21 d), and during the taper (14 d) (see Fig. 1). Mean behavioral activity over the entire recording period was automatically calculated using the Sleepwatch software (Actiwatch activity and sleep analysis version 5.28, Cambridge Neurotechnology Ltd.). Wristwatch actigraphy is a nonintrusive, cost-effective tool used to estimate sleep quantity and quality, which has been compared with polysomnography, showing an accuracy of up to 80% in sleep disordered patients for total sleep time and sleep efficiency (14) and as such is widely used in the sleep literature (22,34). In a recent review on the role and the validity of actigraphy in sleep medicine, Sadeh (28) concluded that according to most studies, actigraphy has reasonable validity and reliability in normal individuals with relatively good sleep patterns.

Sleep–wake scoring can be reliably obtained only with additional information provided in manually completed sleep logs (6). All participants were therefore requested to complete daily sleep diaries. The subjects were asked to record the times of going to bed, falling asleep, waking up, and leaving the bed. In addition, the subjects were asked to mark the time of switching off the light to sleep and wake-up time with a push of the button on the face of the Actiwatch.

Individual nights of sleep were analyzed for the following range of variables: time in bed, bedtime, get-up time, sleep latency, actual sleep time, percent time sleeping while in bed (sleep efficiency), and sleep restlessness (fragmentation index) and immobile minutes. The following dependent variables were derived from the sleep diary and activity monitor data:

  • Time in bed (h): the amount of time spent in bed attempting to sleep between bedtime and get-up time.
  • Bedtime (hh:mm): the self-reported clock time at which a participant went to bed to attempt to sleep.
  • Get-up time (hh:mm): the self-reported clock time at which a participant got out of bed and stopped attempting to sleep.
  • Sleep onset latency (min): the period between bedtime and sleep start.
  • Actual sleep time (h:min): the time asleep from sleep start to sleep end.
  • Sleep efficiency (%): sleep duration expressed as a percentage of time in bed.
  • Fragmentation index: a measure of restlessness during sleep, using the percentage of epochs where activity is >0.
  • Immobile time (min): the actual time spent immobile during time in bed.

The term sleep quality in this investigation is determined by wrist actigraphy by measures of sleep efficiency and fragmentation index; however, this is different from ascertaining sleep quality from sleep stages measured by polysomnography.

To quantify how the training weeks affected the perceived sleep quality, the participants reported their perceived feelings on a seven-point scale, going from very, very good to very, very poor after waking up each morning. In addition, the effect of the training regimen on perceived fatigue was recorded on the morning before each maximal incremental cycling test via a visual 0–100 analog scale (from no fatigue to maximum fatigue).

Illness symptoms

During the 6-wk experimental period, the subjects were required to complete a health questionnaire (URTI symptoms and gastrointestinal discomfort symptoms) on a weekly basis, as performed in previous studies (7,8). They were not required to abstain from medication when they were experiencing illness symptoms, but they were required, on a weekly basis, to report any unprescribed medication taken, visits to the doctor, and any prescribed medications. The illness symptoms listed on the questionnaire were sore throat, inflammation in the throat, runny nose, cough, repetitive sneezing, fever, joint aches and pains, and headache. Two usual items of URTI diagnosis (i.e., muscle soreness and loss of sleep) were not included given that they could be potentially influenced by training overloading and not necessarily the signs of illness. The numerical ratings of light, moderate, and severe (L, M, or S, respectively) were scored as 1, 2, and 3, respectively. In any given week of total symptom, score ≥12 was taken to indicate that a URTI was present. This score was chosen in previous studies (7,8) because to achieve it, a subject would have to record at least three moderate symptoms lasting for 2 d or two moderate symptoms lasting for at least 3 d in a given week. A single URTI episode was defined as a period during which the weekly total symptom score was ≥12 and separated by at least 1 wk from another week with a total symptom score ≥12. Subjects were also asked to rate the impact of illness symptoms on their ability to train (normal training maintained, training reduced, or training discontinued; L, M, or S, respectively). The gastrointestinal discomfort symptoms listed on the questionnaire were loss of appetite, stomach upset, vomiting, abdominal pain, and diarrhea. These symptoms were rated and scored the same way as the illness symptoms (7,8).

Data analysis

As per the methods of previous research (15), the subjects in the OR group were distributed into two subgroups according to their response to the overload period and during the subsequent taper. The triathletes who demonstrated decreased performance (vs Pre) and high perceived fatigue (very tired to extremely tired on the POMS scale) at Mid with subsequent performance restoration or supercompensation were diagnosed as functionally overreached (F-OR group). The remaining subjects in the overload group who maintained or increased their performance after the overload period, despite increased perceived fatigue, were considered acutely fatigued (AF) (21). In addition, because extended monitoring reduces the inherent measurement errors in actigraphy and increases reliability (28), subsequent analyses were conducted using the mean value of each sleep parameter over each week of the training protocol.

Statistical analysis

Normality of data was tested using a Kolmogorov–Smirnov test. Values at baseline for age, weight, height, experience in endurance sport, MAP, and V˙O2max were compared between groups (i.e., CTL, AF, and F-OR) using a one-way ANOVA. Two-way (group × time) ANOVA were used to examine differences in dependent variables (i.e., V˙O2max, RPE, POMS items, perceived sleep quality and actimetry data during sleep) between group means at each time point. When the sphericity assumption in repeated-measures ANOVA was violated (Mauchly’s test), a Greenhouse–Geisser correction was used. If a significant main effect was found, pairwise comparisons were conducted using Duncan’s post hoc analysis. These statistical tests were conducted using Statistica (Version 7.0; StatSoft, Tulsa, OK), and the data are presented as means and SD.


Changes in weekly mean training volume, the distribution of the relative training time spent in the intensity zones and the number of training sessions per week in the three groups during each respective training phase are presented in Table 1. The results demonstrated that the three experimental groups successfully adhered to the prescribed training program and that the AF and F-OR groups increased training volume substantially more than the CTL group (P < 0.001). No significant difference in any training parameters was reported between the AF and the F-OR groups at any periods of the experimental protocol.

Weekly average training volume (mean ± SD), distribution of training intensity, and number of training sessions per week in swimming, cycling, and running during the protocol in the three experimental groups.

Assessment of the OR syndrome

At Pre, all subjects reported low perceived fatigue at rest (i.e., all subjects responded “not at all” or “a little” on the POMS fatigue item), confirming that they were not already in an OR state. Of the 18 overloaded subjects, 9 demonstrated a decrease in performance (−10 ± 4 W) at Mid followed by a performance restoration or supercompensation effect at Post (5 ± 5 W, Table 2). This reduced performance was systematically associated with a concomitant high fatigue score at Mid (i.e., “quite bit” to “extremely” on the POMS fatigue item; Table 2). On the basis of this analysis, these nine triathletes were considered as “functionally OR,” the short-term form of OR (F-OR) (21). The other nine subjects in the overload training group demonstrated higher perceived fatigued but no reduction in performance. According to the nomenclature of Meeusen et al. (21), they were not diagnosed as OR and instead considered AF. Thus, the subsequent results are presented for 9 F-OR subjects (F-OR group), 9 AF subjects (AF group), and 9 control subjects (CTL group). Mean ± SD age, height, and weight were 37 ± 6 yr, 182 ± 6 cm, and 72 ± 9 kg for the CTL group; 35 ± 8 yr, 179 ± 9 cm, and 73 ± 8 kg for the AF group; and 35 ± 5 yr, 180 ± 5 cm, and 72 ± 9 kg for the F-OR group. There were no differences between groups for these descriptive parameters (P > 0.05).

Mean values ± SD at baseline, after the overload period, and after the 2-wk taper in the three experimental groups (control, n = 9; acute fatigue, n = 9; functionally OR, n = 9).

Perceived sleep quality and sleep actigraphy data

Raw values of sleep parameters for the three experimental groups are presented in Table 3. Changes in sleep data from baseline are depicted in Figure 2. There was no significant time–group interaction in perceived sleep quality (P = 0.10), time in bed (P = 0.12), bedtime (P = 0.07), get-up time (P = 0.78), sleep latency (P = 0.13), and fragmentation index (P = 0.07). A significant interaction effect was observed for actual sleep time (P = 0.02), sleep efficiency (P = 0.002), and immobile time (P = 0.006). A progressive decrease of these three parameters was systematically observed only in the F-OR group during the overload period compared with baseline (actual sleep time, P = 0.01; sleep efficiency, P = 0.049; and immobile time, P = 0.005, during the last week of the overload period). All of these parameters were progressively restored to baseline values during the ensuing taper.

Mean values ± SD of weekly sleep actigraphy data during the baseline week, the last week of the overload period, and during the last week of the taper period in the three experimental groups.
Change in mean weekly sleep parameters from baseline values during the overload and taper phase in the three experimental groups. CTL, control; AF, acute fatigue; F-OR, functionally overreached. Gray areas and dashed lines represent 1 CV and 2 CV of the considered parameter during the 6-wk protocol in the control group. *Significantly different from baseline at P < 0.05. Significantly different from the third week of the overload period at P < 0.05.

Infection–symptom incidence

Analysis of illness questionnaires indicated that eight subjects reported at least one episode of URTI during the training overload and/or tapering periods. The occurrence of URTI symptoms during the protocol is presented in Table 4. The proportion of subjects who experienced symptoms of infection was higher in the F-OR group (n = 6, 67% of total infection cases) than that in AF (n = 2, 22%) and CTL groups (n = 1, 11%). No subjects reported symptoms of gastrointestinal discomfort during any phase of the training program.

Occurrence of URTI symptoms during the baseline, the overload, and the taper periods in the three experimental groups (control, n = 9; AF, n = 9; functionally OR, n = 9).


In the present study, we studied nocturnal actimetry in a group of trained triathletes who completed an overload training program followed by a 2-wk taper period and developed symptoms of F-OR in comparison with control counterparts without signs of training intolerance. The most important finding indicated a progressive decrease in the indices of sleep quality, alongside small reductions in sleep quantity, during the overload period in the F-OR athletes, which was progressively reversed during the subsequent taper. Furthermore, a higher prevalence of URTI was also reported in this F-OR group.

Signs of decreased sleep quality in overreached or overtrained endurance athletes have been reported by previous researches. Jurimaë et al. (11) monitored the recovery-stress state in competitive male rowers during a 6-d training camp in response to an average increase in training load by approximately 100% compared with average weekly loads. Using the Recovery–Stress Questionnaire for Athletes (RESTQ-Sport) (13), these authors showed decreased levels of perceived sleep quality, suggesting that recovery may not have been adequate during this training camp, leading to performance impairment and genesis of high perceived fatigue (i.e., overreaching). However, given the lack of objective markers of sleep actimetry, the reliance on perception of sleep quality is problematic to then associate sleep disruption with overloading. In a similar vein, Matos et al. (20) recently reported that frequent perceived sleep problems was one of the most reported physical symptoms by athletes who had experienced persistent daily fatigue and a significant decrement in performance that lasted for long periods. Altogether, these results suggest that heavy load training may exert a negative effect on sleep quality, but to date, limited literature provides objectively measured changes in sleep characteristics during periods of confirmed F-OR.

The novelty of the present research provides objective measures of sleep in a group of trained athletes demonstrating differentiated performance responses (i.e., acute fatigue vs functional overreaching [21]) during a 6-wk training program involving periodic high training load. Time in bed and sleep latency were not different at any period of the training program in the F-OR group; however, these subjects demonstrated a progressive decrease in actual sleep duration, sleep efficiency, and immobile time during the overload period, suggesting substantial sleep disturbances. This finding was reported in at least seven of the nine F-OR athletes for each parameter. During the same period, mean sleep values remained unchanged in the control and in the AF groups. To the best of our knowledge, this study is the first to show such alterations in objective markers of sleep quality during a period of intensified training that resulted in overreaching. Although causation is not inferred, it is possible that sleep disturbance may have been related to mild muscle fatigue or soreness resulting from the high training loads. Certainly given neither bed time, sleep latency or time spent in bed were not significantly altered, and the reduction in sleep duration may result mainly from the lowered efficiency because of difficulty in remaining immobile during sleep. However, despite such measured sleep disruption, subjective quality of sleep remained unaltered, suggesting some disconnect in actual and perceived measures of sleep. Indeed, despite eight of the F-OR athletes reporting reduced scores for perceived sleep quality, the magnitude in change was insufficient to reach statistical significance.

Although the results suggest that F-OR athletes demonstrated a modest decrease in quality and quantity of sleep during the overload period, it remained considerably better than that experienced by sleep disorder patients (29), extreme sleep deprivation (32), or by athletes in response to jet lag (18) or hypoxic exposure (26). In addition, Halson et al. (9) reported larger sleep deficiency during leading to overtraining (<6 h per night) in a talented female sprint cyclist who developed signs of overtraining (i.e., persistent feeling fatigued and underperforming over months). The actual sleep time in the F-OR subjects during the overload training period remained higher than the values reported by Leeder et al. (17) in a cohort of elite athletes under normal training conditions. Nevertheless, we cannot exclude that the moderate changes observed in the F-OR during the present experiment would not unduly affect performance in elite athletes, where very small differences in performance can have large impact on the competition issue (25). It remains also unclear during the present study whether sleep disturbance was an etiological mechanism of overreaching or simply just a symptom. Regardless, it is acknowledged that the reduction in sleep duration during F-OR was small in the spectrum of sleep disturbances and may suggest that sleep monitoring to detect F-OR may require extended periods of data collection. Further research is required to determine the relationship of sleep with training tolerance and adaptation, especially in athletes developing training maladaptations (i.e., overreaching and overtraining).

Given the purported relationship between prolonged reductions in sleep quality and quantity with increased risk of illness, it was interesting to observe a higher infection rate in the F-OR subjects during the present experiment. Of the nine F-OR athletes, five reported increased URTI symptoms during the overload period and concurrent to the noted sleep disturbances, whereas only two cases were observed in the AF and CTL groups during the same period. Interestingly, this illness prevalence was the highest during the last week of the overload period, which is temporally aligned when sleep disturbances reached their highest magnitude during the study, perhaps implying an accumulative effect. The observed decrease in sleep and increase in URTI during F-OR is in accordance with several previous studies reporting both innate and adaptive immunity are depressed during sustained periods of heavy training (38). This association suggests there is a link between the recuperative processes of sleep and the immune system (27). The current study provides supporting evidence that high volume training periods may result in increased URTI, alongside reduced sleep quality. However, again whether sleep disturbance was an etiological mechanism of URTI development as a result of overreaching or simply coincidental symptoms remains to be elucidated, particularly given the relatively small reductions in sleep durations reported.

In conclusion, F-OR athletes showed objective signs of moderate sleep disturbances and higher prevalence of infections in the present study. These results were in conrast with control counterparts who did not demonstrate any symptoms of training intolerance during the protocol. Whether poor sleep was a consequence of increased training causing the development of overreaching or whether sleep disturbances were simply symptoms of OR remain unclear. Whatever the causative link between F-OR and sleep, we suggest that endurance athletes should be encouraged to ensure ideal sleeping environment (quiet, cool, and dark) (5) and to avoid early morning schedule (31), when they are exposed to high training load. Napping for short periods during the day may also represent a recommended recovery strategy for athletes to compensate the potential decline in actual sleep time associated with development of F-OR. Further investigations are required to confirm this hypothesis and to investigate the importance of sleep and its relationship with overreaching.

This study was made possible by a technical support from the French Federation of Triathlon. The authors are especially grateful to Frank Bignet and Benjamin Maze for their help and cooperation. The authors received funding for research on which this article is based from the French Ministry of Sport and the French National Institute of Sport, Expertise and Performance (Paris). The authors report no conflict of interest.

The results of the present study do not constitute endorsement by the American College of Sports Medicine.


1. Bishop D, Jenkins DG, McEniery M, Carey MF. Relationshipbetween plasma lactate parameters and muscle characteristics in female cyclists. Med Sci Sports Exerc. 2000; 32 (6): 1088–93.
2. Bosquet L, Montpetit J, Arvisais D, Mujika I. Effects of tapering on performance: a meta-analysis. Med Sci Sports Exerc. 2007; 39 (8): 1358–65.
3. Cohen S, Doyle WJ, Alper CM, Janicki-Deverts D, Turner RB. Sleep habits and susceptibility to the common cold. Arch Intern Med. 2009; 169 (1): 62–7.
4. Driver HS, Taylor SR. Exercise and sleep. Sleep Med Rev. 2000; 4 (4): 387–402.
5. Duffield R, Murphy A, Kellett A, Reid M. Recovery from repeated on-court tennis sessions: combining cold water immersion, compression and sleep recovery interventions. Int J Sports Physiol Perform. 2014; 9 (2): 273–82.
6. Fietze I, Strauch J, Holzhausen M, et al. Sleep quality in professional ballet dancers. Chronobiol Int. 2009; 26 (6): 1249–62.
7. Gleeson M, Bishop NC, Oliveira M, McCauley T, Tauler P, Lawrence C. Effects of a Lactobacillus salivarius probiotic intervention on infection, cold symptom duration and severity, and mucosal immunity in endurance athletes. Int J Sport Nutr Exerc Metab. 2012; 22 (4): 235–42.
8. Gleeson M, Bishop NC, Oliveira M, Tauler P. Daily probiotic’s (Lactobacillus casei Shirota) reduction of infection incidence in athletes. Int J Sport Nutr Exerc Metab. 2011; 21 (1): 55–64.
9. Halson S, Martin DT, Gardner AS, Fallon K, Gulbin J. Persistent fatigue in a female sprint cyclist after a talent-transfer initiative. Int J Sports Physiol Perform. 2006; 1 (1): 65–9.
10. Halson SL, Jeukendrup AE. Does overtraining exist? An analysis of overreaching and overtraining research. Sports Med. 2004; 34 (14): 967–81.
11. Jurimae J, Maestu J, Purge P, Jurimae T. Changes in stress and recovery after heavy training in rowers. J Sci Med Sport. 2004; 7 (3): 335–9.
12. Jurimae J, Maestu J, Purge P, Jurimae T, Soot T. Relations among heavy training stress, mood state, and performance for male junior rowers. Percept Mot Skills. 2002; 95 (2): 520–6.
13. Kellmann M, Kallus KW. Recovery–Stress Questionnaire for Athletes. Champaign: Human Kinetics; 2001. p. 112.
14. Kushida CA, Chang A, Gadkary C, Guilleminault C, Carrillo O, Dement WC. Comparison of actigraphic, polysomnographic, and subjective assessment of sleep parameters in sleep-disordered patients. Sleep Med. 2001; 2 (5): 389–96.
15. Le Meur Y, Hausswirth C, Natta F, Couturier A, Bignet F, Vidal PP. A multidisciplinary approach to overreaching detection in endurance trained athletes. J Appl Physiol. 2013; 114 (3): 411–20.
16. Le Meur Y, Pichon A, Schaal K, et al. Evidence of parasympathetic hyperactivity in functionally overreached athletes. Med Sci Sports Exerc. 2013; 45 (11): 2061–71.
17. Leeder J, Glaister M, Pizzoferro K, Dawson J, Pedlar C. Sleep duration and quality in elite athletes measured using wristwatch actigraphy. J Sports Sci. 2012; 30 (6): 541–5.
18. Leeder JDC, Gardner AS, Foley S, van Someren K, Pedlar CR. The effect of jet lag on parameters of sleep in elite divers quantified by actigraphy. Med Sci Sports Exerc. 2009; 41 (5): 57–8.
19. Mac Nair D, Lorr M, Droppleman L. Profile of Mood States Manual. San Diego: Educational and Industrial Testing Service; 1971. p. 27.
20. Matos NF, Winsley RJ, Williams CA. Prevalence of nonfunctional overreaching/overtraining in young English athletes. Med Sci Sports Exerc. 2011; 43 (7): 1287–94.
21. Meeusen R, Duclos M, Foster C, et al. Prevention, diagnosis, and treatment of the overtraining syndrome: joint consensus statement of the European College of Sport Science and the American College of Sports Medicine. Med Sci Sports Exerc. 2013; 45 (1): 186–205.
22. Miller NL, Shattuck LG. Sleep patterns of young men and women enrolled at the United States Military Academy: results from year 1 of a 4-year longitudinal study. Sleep. 2005; 28 (7): 837–41.
23. Myllymaki T, Kyrolainen H, Savolainen K, et al. Effects of vigorous late-night exercise on sleep quality and cardiac autonomic activity. J Sleep Res. 2011; 20 (1 pt 2): 146–53.
24. Nederhof E, Lemmink KA, Visscher C, Meeusen R, Mulder T. Psychomotor speed: possibly a new marker for overtraining syndrome. Sports Med. 2006; 36 (10): 817–28.
25. Paton C, Hopkins WG. Competitive performance of elite Olympic-distance triathletes: reliability and smallest worthwhile enhancement. Sportscience. 2005; 9: 1–5.
26. Pedlar C, Whyte G, Emegbo S, Stanley N, Hindmarch I, Godfrey R. Acute sleep responses in a normobaric hypoxic tent. Med Sci Sports Exerc. 2005; 37 (6): 1075–9.
27. Reilly T, Edwards B. Altered sleep–wake cycles and physical performance in athletes. Physiol Behav. 2007; 90 (2–3): 274–84.
28. Sadeh A. The role and validity of actigraphy in sleep medicine: an update. Sleep Med Rev. 2011; 15 (4): 259–67.
29. Sadeh A, Acebo C. The role of actigraphy in sleep medicine. Sleep Med Rev. 2002; 6 (2): 113–24.
30. Samuels C. Sleep, recovery, and performance: the new frontier in high-performance athletics. Neurol Clin. 2008; 26 (1): 169–80; ix-x.
31. Sargent C, Halson S, Roach GD. Sleep or swim? Early-morning training severely restricts the amount of sleep obtained by elite swimmers. Eur J Sport Sci. 2014; 14 (Suppl 1): S310–5 .
32. Skein M, Duffield R, Edge J, Short MJ, Mundel T. Intermittent-sprint performance and muscle glycogen after 30 h of sleep deprivation. Med Sci Sports Exerc. 2011; 43 (7): 1301–11.
33. Smith RS. Sleep Deprivation: Clinical Issues. Pharmacology and Sleep Loss Effects. New York: Marcel Dekker; 2005. p. 589.
34. Stanley N. Actigraphy in human psychopharmacology: a review. Hum Psychopharmacol. 2003; 18 (1): 39–49.
35. Taylor SR, Rogers GG, Driver HS. Effects of training volume on sleep, psychological, and selected physiological profiles of elite female swimmers. Med Sci Sports Exerc. 1997; 29 (5): 688–93.
36. Urhausen A, Kindermann W. Diagnosis of overtraining: what tools do we have? Sports Med. 2002; 32 (2): 95–102.
37. Vgontzas AN, Zoumakis E, Bixler EO, et al. Adverse effects of modest sleep restriction on sleepiness, performance, and inflammatory cytokines. J Clinical Endocrinol Metab. 2004; 89 (5): 2119–26.
38. Walsh NP, Gleeson M, Pyne DB, et al. Position statement. Part two: maintaining immune health. Exerc Immunol Rev. 2011; 17: 64–103.


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