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Understanding Stretch Shortening Cycle Ability in Youth

Sahrom, Sofyan B. BSc(Sports Science), PGDip(Physical Conditioning)1; Cronin, John B. PhD; Harris, Nigel K. PhD2

Strength and Conditioning Journal: June 2013 - Volume 35 - Issue 3 - p 77–88
doi: 10.1519/SSC.0b013e318295560a


1Performance Enhancement Institute, Singapore Sports School, Singapore; and

2Sports Performance Research Institute New Zealand (SPRINZ), Auckland University of Technology, Auckland, New Zealand

Conflicts of Interest and Source of Funding: The authors report no conflicts of interest and no source of funding.



Sofyan B. Sahromis a strength and conditioning coach with the Singapore Sports School.



John B. Croninis a professor of Strength and Conditioning at Auckland University of Technology and holds an Adjunct Professorial Position at Edith Cowan University.



Nigel K. Harrisis a senior lecturer in Sport and Exercise Science at Auckland University of Technology and a Strength and Conditioning Coach.

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In human locomotion, such as running, hopping, and jumping, muscle contraction is typified by a combination of eccentric lengthening followed immediately by a concentric-shortening contraction thus termed a stretch-shortening cycle (SSC). The stretching of a muscle is only considered an eccentric action if the muscle is active during the stretch (36,37). According to Komi and Gollhofer (39), an effective SSC requires 3 fundamental conditions: (a) a well-timed preactivation of the muscles before the eccentric phase, (b) an eccentric action phase that must be short and fast, and (c) an immediate transition or short delay between the eccentric and concentric phase. The improvements in performance by the use of SSC muscle actions are well documented in the literature.

One of the most used methods to demonstrate the SSC augmentation is by comparing 2 different types of vertical jumps (no arm swing). A vertical jump that is preceded by a countermovement (i.e., a countermovement jump [CMJ]) can be compared with a vertical jump without a countermovement (i.e., a squat jump [SJ]). In most studies using this approach, the CMJ has led to better vertical jump performance than the SJ, by between 18 and 30% in adults (11,38). Although the enhancements from the potentiating effects of the SSC are certain, the underlying mechanisms responsible for this potentiation have been a source of debate for many years.

These different viewpoints were summarized in an article with subsequent discussions by van Ingen Schenau et al. (84,85). Four possible explanations for the SSC enhancement were presented. First, it was proposed that SSC enhancement is because of the storage and utilization of elastic energy in the muscle, particularly the series elastic component (SEC). Second, the countermovement simply provided time for the muscles to build up to a maximum active state before the commencement of the concentric contraction. Third, it was theorized that alteration of the properties of the contractile machinery occurred during the prestretch of the active muscle, which subsequently enhanced the concentric contraction. The contributions of the spinal reflexes were proposed as the fourth possible explanation for SSC potentiation. Spinal reflexes that are triggered by the prestretch of a muscle during a countermovement help to increase muscle activation during the concentric phase (20). The reader is directed to the discussion and subsequent commentary by van Ingen Schenau et al. (84) for a full treatise of these explanations of SSC potentiation.

A good understanding of SSC in youth will help coaches develop better plyometric programs for children as part of a long-term development approach. To do so, an understanding of growth and maturation is first required before proceeding to the active and passive components of SSC and how the components possibly change with maturation and the subsequent effects on SSC ability.

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Irrespective of the underlying mechanisms, SSC potentiation is undeniable and a great deal of research has investigated CMJ and SJ performance in adults. However, there has been less literature that has investigated these jumps in preadolescent and adolescent youths. The biological maturity of youths does not necessarily coincide with their chronological ages and can differ by several years (2,54,55). Youths undergoing puberty experience many physiological changes, which include changes to their musculotendinous and neuromuscular systems (53). The physiological changes during these periods of maturity are likely to contribute to age-associated variations in jumping performances among children of different age groups, maturity level, and gender (12,53,81).

Spurts in growth and performances are likely to occur during adolescence (53). Adolescence is generally viewed as occurring between the ages of 12 and 18 years where great physical and mental development occurs, such as puberty. There is a large amount of change occurring during these years and great variability in the rate of growth among individuals. Therefore, it is important to note the biological age of an individual rather than the chronological age. Biological age as opposed to chronological age is determined by the youth’s rate of development and maturational process. This maturational process can be further divided into 3 significant phases: prepubescence, pubescence, or postpubescence with each phase having unique characteristics.

Prepubescents are usually chronologically above 8 years of age but have not yet reached the pubescent stages. This maturation phase is the buildup phase before the puberty phase and is marked by accelerated growth and the appearance of secondary sex characteristics, but they are not fully capable of sexual reproduction (53,80).

Pubescents are defined as children who are at the onset of puberty, have developed secondary sex characteristics, and have reached maturity (21,53,80). Also known as adolescents, they are usually chronologically between 13 and 17 years of age for males and between 12 and 16 years of age for females. One of the most recognized events signifying children in this maturation stage would be the increase in stature or adolescent growth spurt. During this adolescent growth spurt, the standing height (increase in) velocity increases and peaks, commonly known as peak height velocity (PHV). PHV values range from 5.4 to 11.2 centimeters per year for females and from 5.8 to 13.1 centimeters per year for males (63). Practitioners can take note of this height increase and use regular height monitoring as a practical method for gauging biological age. There are of course other methods of height monitoring that are shown in Table 1.

Table 1

Table 1

Postpubescents are usually chronologically above 17–18 years of age for males and 16–17 years of age for females. The skeletal growth slows and the physiologic functions of the sexual organs are fully established (53,80). Ideally, children should be classified and trained according to their biological maturity or developmental stages. For this review, the term youth shall be referred to individuals below the age of 18 years. Other terms such as adolescents, pre, post, and pubescents refer to individuals as described above.

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Because of the ease of measuring vertical jumps, different methodological approaches have been developed to measure SSC enhancement using the vertical jump by comparing CMJ with SJ (38). CMJ uses a countermovement, whereas SJ does not; in theory, the difference between the 2 types of vertical jumps can be attributed to augmentation associated with the countermovement, i.e., SSC augmentation. Table 2 provides in detail the 4 common field-based methods of quantifying SSC augmentation that are easy to use.

Table 2

Table 2

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Hill (32) in 1938, in his original experiment on the thermodynamics of muscle contraction, described a 2-component model of muscle that consisted of a contractile component (CC) and a purely elastic element that lies in series with the CC known as the SEC. Over the years, the model was extended into a 3-component model (22,25), where another elastic component known as the parallel elastic component (PEC) was added. The addition of the third component was introduced to help explain the passive force of an inactive fiber. The model attempts to describe characteristics rather than direct reference to any individual structures. Therefore, each component can comprise many different muscle structures that possess those characteristics. The CC of the model refers to the moving or contracting components or structures of muscles (i.e., the muscle fibers: actin and myosin filaments) that provide the active force during contraction of the muscle.

The SEC refers to the structures of the muscle, which lies in series or in line with the muscle fibers such as cross-bridges, structural proteins, and tendons. The PEC is noncontractile in nature and lies parallel to the muscle fibers. A relaxed passive muscle exerts the force that it contributes when it is stretched beyond its resting length. Muscle connective tissues such as the perimysium, epimysium, and endomysium are examples of the PEC.

During human locomotion, such as walking, running, or jumping, the 3 components interact to produce efficient motion. For example, in the initial eccentric phase of a CMJ, the CC is active, the SEC and PEC are being lengthened, and as a result, elastic energy is stored. In the ensuing concentric contraction, the stored elastic energy is used in conjunction with the contractile forces being produced in the CC. The magnitude of the energy returned is proportional to the applied force and induced deformation with reported energy returns of between 65 and 85% in human tendons (7,70). The contribution of the SEC and PEC is minimized if the squat position is held for approximately 4 seconds before the concentric phase (90). The assistance of elastic energy is likely to exist even for SJ; however, when starting from a static squat, most of the elastic energy is dissipated as heat energy, and therefore, the forces associated with the ensuing concentric contraction are primarily attributed to the CC. These factors that occur in most cases during SJ (extended duration) are thought to be one of the main reasons why SJ is inferior to CMJ performance, i.e., minimal contribution of SEC and PEC. The Figure highlights the difference in force profile between a CMJ and a SJ.



Each of the components contributes to total force production during the SSC. However, it has also been observed that the mechanical properties of the SEC and the PEC were not related to each other (41). Among the 3 components, it is likely that the main contributors of the propulsive force during the SSC lie more with the SEC and the CC because of these components' response to deformation and ability to store potential energy. The magnitude of the PEC contribution is currently debatable (83). Nonetheless, the following sections discuss how the contributions of the active (CC) and passive (SEC and PEC) components change with maturation and the subsequent effects on SSC ability.

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Other than changes in muscle mass and fiber-type proportions, the exact changes that occur in the contractile properties of muscle during puberty are relatively unknown as there have been few studies that have investigated these changes. Activation ability of a muscle refers to the individuals’ ability to successfully recruit and activate the motor unit during a movement. When more motor units are able to be activated for a movement, the muscle is able to generate a higher amount of force. It has been consistently shown that youths have a lower voluntary muscle contraction ability or maximum voluntary contraction (MVC) than adults (3,18,56). Furthermore, the magnitude of twitch tension (TT) and MVC are 2 of the main changes that have been found to increase with age and maturity in children (10,18,56–58). Comparisons of the extensor hallucis brevis muscle in male subjects aged between 3 and 22 years clearly demonstrated that maximal isometric TTs increased gradually as the individual matured (57). This improvement, although gradual at first, undergoes a significant marked increase during puberty.

Differences in the maturity and development of the muscle groups can be observed as early as 6 years of age. Belanger and McComas (5) conducted a study to determine the extent of the changes of contractile properties of the ankle muscles during childhood (6–13 years old, n = 10) and adolescence (15–18 years old, n = 8). A strong and positive relationship was observed in children between age and MVC torque values for both ankle dorsiflexion (r = 0.78) and plantar flexion (r = 0.76). The same relationship was also observed for twitch torque and age for both children (r = 0.81) and adolescents (r = 0.81). The mean values were approximately double the values for the adolescent (148.9 N·m) compared with the younger children (78.3 N·m). However, no significant correlations were found between age and contraction time. The authors concluded that these differences were likely because of the fiber-type proportions between the dorsiflexion and plantar flexor muscles (6) and possibly other variables such as active state and myosin light chain phosphorylation (62).

The results of the study by Belanger and McComas (5) further support the concept of age-related differences for the CCs, which is also observed for motor unit activation although it was partial. The younger the child, the less voluntary activation the individual has (10,18). Davies et al. (18) observed that there was a relationship in voluntary muscle ability and age (r = 0.93). The study also reported that younger children (preadolescent) take a longer time to reach peak tension as opposed to older children (adolescent) and adults when electrically stimulated. Blimkie et al. (10) compared the degree of motor unit activation during voluntary contraction in a group of males between the ages of 10 and 16 years. No significant difference in elbow flexor percentage of motor unit activation among the age groups (89.4 versus 89.9%) was found. However, there was a significant difference for the knee extensors (77.7 versus 95.3%). Although these findings are conflicting (lower body only) compared with other studies, it seems that age-associated variance exists.

When compared with adults, motor unit activation or neurological adaptations are likely to be one of the primary adaptations to strength training adaptations in prepubescents (10,40,66,73). Ozmun et al. (66) used electromyography (EMG) to measure strength training–induced changes in prepubescent boys and girls after 8 weeks of strength training. The authors observed significant increases in both maximal isokinetic strength (27.8%) and a corresponding increase in integrated EMG amplitude of 16.8% with no corresponding significant increase in muscle size, suggesting that the youths in the study experience a neurological adaptation as opposed to hypertrophy. Ramsay et al. (73) and Blimkie et al. (10) investigated the contribution of changes in motor unit activation to training-induced strength increases in prepubescent boys. In both studies, there was a corresponding increase in motor unit activation with strength change, although in terms of percentage increase, motor unit activation was not proportionate and much less than the increase in strength. Although many factors (e.g., hypertrophy) can contribute to strength training adaptations, in prepubescents, motor unit activation is likely to be the primary factor for strength training adaptations.

Although some contractile properties gradually increase with age, it has also been suggested that other contractile properties of muscle may have already matured by early childhood (57,73). McComas et al. (57) observed that the twitch contraction times of younger children (2–16 years of age, n = 19) were already within adult range. The same observation was also made for the ratio of muscle strength to muscle cross-sectional area, which is used to indicate maturity of the contractile properties. For some muscle groups such as the knee flexors, the ratio remains relatively consistent throughout the different maturational groups. For other muscle groups (e.g., the elbow flexors), the ratio increases as the individual ages through his/her adolescent years (57). Although the study population was small (n = 19), the authors did observe a noticeable increase, which, although inconclusive, does add support to the suggestion of early maturation of the contractile properties. This increase suggests that the growth of contractile force increases at a much greater rate than the increase in muscle mass or the ability to develop voluntary maximum force during adolescent growth.

Stretch reflex potentiation has been observed to be related to age or maturity level (24,28,49). Grosset et al. (28) attempted to observe the development of reflex excitability in prepubescent children. They believed that although the central mechanism that controls stretch reflex in children is mature by the time they reach prepubescence, the mechanically induced reflex only increases with the age of the child. Lin et al. (49) in their study observed that reflex twitch time also improved as an individual matures before it slowly deteriorates again as one grows older. It has been suggested that this increase is because of the maturation of the sensorimotor pathways (49). Other possible contributors to the development of the stretch reflex could possibly be improved spindle sensitivity and/or increased gamma drive (γ) of the muscle spindles (28). Grosset et al. (28), who observed changes in stretch reflex and muscle stiffness in children, also suggested that elastic properties of muscle (and in relation to muscle stiffness), which decreased as the individual matured, was likely one of the major contributors to the development of the stretch reflex because of the correlation between the changes in reflex amplitude and active muscle stiffness. Changes in passive muscle stiffness with maturation are explored in detail in the next section.

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Because of the importance of the SEE and muscle stiffness in the SSC, it is important to investigate this phenomenon in youth. Previous studies on both deceased donors and animal cadavers have shown that there are changes in the elastic properties across ages (17,23,41,42,64,78). Differences in mechanical stiffness between maturational groups can differ from 84% to as much as 334% (23,64). Elliot (23) in 1965 observed that the tensile strength of the male human tendon for infants was 30 and 100 MPa in adults, a difference of about 334%. This difference in tendon stiffness (patella) reduces as the child matures and by the age of 8–9 years has reduced to 94% between men and boys and 84% between women and girls (64). The same pattern was also observed for the Young’s modulus with a difference of 99% between men and boys and 66% between women and girls. Young’s modulus describes the ratio of stress to strain and refers to the soft tissue ability to withstand changes in length during lengthwise tension. The investigators concluded that an increase in mechanical stiffness between human children and adults is because of the change in stiffness of the tendon microstructures.

Kubo et al. (42) investigated tendon compliance of 3 different age groups. Significant differences in muscle compliance were found among younger boys, older boys, and adult men (Table 2). The tendon structures of the younger children were reported to have the highest compliance, whereas adults were reported to have the highest stiffness. Significantly higher tendon stretch was also noted for the younger boys with muscle forces above 0.35 MPa of Fm per muscle cross-sectional area than the other 2 groups. There was no significant difference when comparing the tendon stretch between the older boys and the adults. Stiffness was defined by Kubo et al. (42) in his study as the relationship between the estimated muscle force and tendon elongation during the ascending phase of a leg extension. This observation regarding muscle/tendon compliance in youth is supported by other studies, some of which has been highlighted in Table 3 (28,42,49,51,52,87).

Table 3

Table 3

Two main reasons have been suggested to explain the increase in tendon stiffness. The first is because of the increase in tendon mass and therefore the anatomical cross-sectional area and tendon length. One of the contributors to increase in tendon size and cross-sectional area is probably the increase in the collagen fibril diameter itself as the individual matures (19,67). This combined with other normal growth changes such as increases in muscle size and mass leads to an increase in the loading on the tendon itself. This combination of growth and loading in turn leads to an increase in tendon stiffness during maturation (17,64). Other than pure increase in overall mass, other changes have also been noted such as microstructural changes in the tendon (4,19,65,67,68,74), increases in the fibril density or packing, and increases in the cross-linking within the collagen (4,74).

The second reason for increasing stiffness has been attributed to the reduction of collagen crimping, which is another microstructural change of the tendon that contributes to increased stiffness. Collagen fibers are packed in parallel; however, they are not straight but wavy (19,75). The crimp is a structural characteristic that refers to the “waviness” of the fibril, which contributes to the nonlinear stress-strain relationships. A nonlinear stress-strain means that the stiffness of the soft tissues changes with deformation increasing the effect, as opposed to a linear relationship where the stiffness remains constant. As the collagen fibrils become “uncrimped,” tendon stiffness increases, contributing to the overall stiffness of the tendon. Studies on both humans and animals have shown that there is a reduction in collagen crimping with increased age from youth to adult (35,69).

Aponeuroses are broad flat membranes that are histologically similar to tendons but lack the same level of blood supply and nerves. Whereas tendons connect muscle to bone, aponeuroses connect muscles to the part that moves, be it bone or other muscles. Aponeuroses undergo a similar progressive development from childhood to adulthood (13,42) and are likely to have an effect on the storage of elastic energy. The aponeuroses for those younger than 16 years were found to be slender, shorter, and lower volume (13,43). The length of the aponeuroses appeared to increase with age (42). Adults above the age of 40 years were consistently found to have much thicker aponeuroses (13). However, the aponeuroses for an elderly group (60 years and older) were still particularly well developed and strong. This observation supports the concept of function over age for the aponeuroses similar to muscles.

In summary, children have more compliant tissues, which stiffen as the individual matures. This is likely to play a role in the SSC ability of youths, the extent of its effect however is unknown. The extent of its trainability is also difficult to assess and differentiate be it because of maturation or training. It should be noted that even research into adult stiffness/compliance and the effect on force production is conflicting. For example, a compliant tissue will store more energy and perform more work if contraction time allows this to occur, whereas when contraction durations are brief as in the case of foot strike when sprinting, a stiffer musculotendinous unit that is capable of higher rates of force development is desirable (45,47,48). It is likely that there is an optimal range of stiffness/compliance that is best for specific tasks; however, more research is needed in this area for both adults and youth. Practitioners might want to take this into consideration when attempting to target and train stiffness in youths.

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The magnitude of potentiation that results from the prestretch augmentation cited in the previous literature was from research using mainly adults. Youths, specifically adolescents and preadolescents, who have yet to reach full maturity in terms of the development of muscle, tendon, and/or reflexes may not have the same level of potentiation. This section explores this theme in more detail.

A number of studies have attempted to compare the jumping performance of children with adults (29,87,88). Wang et al. (88) compared CMJ performance of prepubescent children (6 ± 0.41 years) with adults (18 ± 0.50 years). The authors found significant differences in the range of motion for the jump, particularly the depth of the crouch during the countermovement, and a more backward projection (in reference to the line of center of gravity) during takeoff for the prepubescent children. These differences were because of limited range of movement (ROM) during the crouch and what the authors termed as immature joint functions at the knee before takeoff (88).

Limited ROM in the ankle and knee of the children during the takeoff has been observed (57) and is likely indicative of low ability to perform the jump, possibly because of a lack of experience in performing the jump or possibly a physical limitation (less likely). Immature joint function refers to different firing patterns in the children compared with the adults. To descend into the crouch, children used mainly concentric contractions of the joint flexors compared with adults who used both concentric contractions in the joint flexors and eccentric contractions in the joint extensors. Such differences were attributed to probable lack of form in jumping strategy because of experience and immature joint function. It is also possible that the lack of coordination could reflect a motor system that is unable to exploit the SSC at the current stage of maturation. Therefore, any future studies with children should include a strict familiarization jump session before the study or prior jump experience to help tackle the lack of form in jumping strategy.

Harrison and Gaffney (29) conducted a study to observe the effects of age and gender on SSC performance. The vertical jump performance of prepubescent children (n = 20) consisting of 12 girls (6 ± 0.4 years) and 8 boys (6 ± 0.2 years) was compared with adults (n = 22) consisting of 12 women (21 ± 1 years) and 10 men (23 ± 3 years). The SSC potentiation was calculated by comparing the differences between CMJ and SJ collected from a force plate. The variable used to compare the difference was the ratio of velocity at takeoff ([INCREMENT]VTO) derived from the resultant ground reaction force on the force plate. The children had a percentage difference in [INCREMENT]vTO of 10.5 ± 19.7%, which was higher than the adult group that had [INCREMENT]vTO of 6.3 ± 5.6%. However, it should be noted that there was great variability in the [INCREMENT]vTO of children and that there was a noticeable difference in scores between boys (14.5 ± 24.9%) and girls (7.8 ± 15.1%). It was believed that one of the primary reasons for this difference was because of the poor execution and performance of the SJ, rather than SSC-augmented improvement in the CMJ (29).

The researchers proposed 3 reasons in support of their conclusion. First, a lower or reduction in variability is an indication of motor development, learning, and maturity; therefore, a greater variation as observed in the children suggested a less-developed or mature motor pattern. This variability was again observed in the high ΔvTO scores of the SJ for the children. The variability suggested nonoptimal performance of SJ, which was consistent with what was observed by Bobbert et al. (11). The second observation reported was that when comparing CMJ with SJ, the children generated a significantly greater relative peak power and force for CMJ (Table 4). Children also generated significantly lower peak power (28 ± 3 W/kg) in SJ when compared to adults (48 ± 7 W/kg) with similar results for peak force (Table 4). These results suggest lower motor development or mastery of SJ compared with CMJ. The third reason was that significant variations were observed in relative peak force in SJ for children compared with adults, which again suggests reduced motor control or mastery of SJ compared with CMJ, and that it is possibly age dependent. In both situations, poor execution of SJ would increase the ratio of ΔvTO between CMJ and SJ.

Table 4

Table 4

The variability in jumping performances observed by Harrison and Gaffney, which is suggestive of motor control issues related to maturity, has been observed in many other studies on jumping in youth (26,30,33,50,61,88). The variability could also possibly suggest an inability to exploit SSC. However, from a coaching standpoint, it is likely that motor control or a lack of skill is one of the main causes of variability. Practitioners might want to focus on coaching good jumping and landing technique first (1,15). This would at least eliminate or minimize the variability because of motor control issues and minimize injury risk associated with jumping and landing (60,71,72,89). Future research measuring SSC enhancement (SJ versus CMJ) in youth populations needs to take into account these issues and ensure that the youth subjects are proficient in both methods of jumping.

Most literature comparing CMJ with SJ in children has shown CMJ to be superior, which is to be expected. Observations from recent research (51) have suggested that this might not always be the case, at least for jump height. The jumping performances and SSC ability (CMJ versus SJ) of children across chronological ages of 7–17 years were measured. Periods of accelerated adaptation in SSC across the ages of 14–16 years were observed. However, in the same study, it was also observed that children aged 12–14 years had a better mean SJ jump height (centimeters) compared with CMJ. Children, 15 years of age, had the same jump height performance between CMJ and SJ. These children could possibly be post-PHV. Although the investigators did not directly address the superiority of SJ performance compared with CMJ, it was suggested that because these ages were post-PHV, it could be due to a combination of an increase in maximal isometric strength and concentric strength capability of the subjects as opposed to their SSC ability. Post-PHV is a period where it has been observed that there is an increase in strength and muscle mass (9). Because maximal isometric strength regardless of age is believed to be proportional to muscle size (82), it is possible that the greater maximal isometric strength combined with increased concentric ability might explain why the mean SJ height performance was better than CMJ during ages of 12–14 years. It is likely that after the age of 16 years, when the children are more mature, they exhibit the expected adult-like CMJ versus SJ jump performance.

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Certain neuromuscular and musculotendinous changes do occur with maturation, but the influence of these changes on SSC ability of youth is not yet clear. This is because the biological maturity of youth does not necessarily coincide with chronological age, and therefore, the variability in SSC ability across different populations is likely to exist. No studies have directly investigated SSC augmentation for jumping potentiation across maturation, i.e., pre, at, and post pubescence. The more compliant tissues evident in children, which stiffen as they mature, are likely to play a role in the SSC ability of youths. Thus, measuring SSC potentiation in children and determining if SSC potentiation differs across maturational stages would provide an insight into the optimal windows for trainability of the SSC. Better understanding windows of trainability should enable development of programs for children to optimize their SSC ability as part of long-term development of youth athletes.

Practitioners, looking to assess SSC ability in youth practitioners, might want to consider 2 main factors: the first would be the biological maturity of the youth and the second would be the method. Practitioners can use any of the methods highlighted for assessing biological age (Table 1) and SSC ability (Table 2). One of the methods highlighted is the eccentric utilization ratio (EUR), which is essentially the ratio of CMJ in relation to SJ calculated by taking the displacement of CMJ and dividing it by the displacement of SJ, resulting in a ratio, the EUR. It is expected that adult athletes will have an EUR of at least 1.0 (27), which suggests a poor SSC augmentation ability. A higher EUR would suggest that the athlete possesses a high SSC augmentation ability. The EUR can also be measured using other outputs. If there is access to a force plate or position transducer, outputs such as peak and mean power can be used. The additional advantage of monitoring peak power (EUR) on top of monitoring the SSC augmentation ability will also allow the coach to monitor increases in actual power production with training and as the adolescent matures. This is especially important for monitoring adolescents who are still growing and are likely to experience changes in mass. Unlike adults, jumping performance in youths is not as stable with great variability and lack of familiarization with the jump itself. For youths, learning effects and the subsequent increased jump efficiency might lead to sudden increase in jump displacement in a very short period with or without the necessary increase in power production capability. These reasons combined could serve as a better monitoring tool of performance to those coaching youths and provide another additional advantage of using EUR peak power.

It is important to note that the EUR for children might differ depending on the familiarity with the SJ. One of the consistent observations found in jump studies using youth subjects is the variability in jumping performance, particularly in SJ owing to motor control issues related to maturity. Without any intervention or specific familiarization, it is likely that children will not exhibit SJ performances typically observed in adults until they are much more mature, leading to a misleading and usually an inflated value. Therefore, it is recommended that when comparing CMJ and SJ performance in children, a familiarization jump session should be included and research should ideally use children with some prior jump experience.

It is suggested that practitioners working with youths looking to develop SSC-related ability such as jumping and other plyometric type of training might want to focus on 2 aspects, which combined would likely allow for a better jump performance. The first would be the development of good sound jumping and landing techniques as many of the studies reviewed have highlighted the variability of jumping performance of youth. The development of good technique will minimize the variability and improve the coordination of the jumping pattern (1,15). This might possibly lead to an improvement in the motor pattern to better exploit SSC. A sound muscle strengthening program concurrent or before a serious plyometric program might also lead to an improvement. The improvement in the jumping technique and improvements in muscular strength not only allow for a better jump performance but also minimize the risk of injury to the youth.

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    stretch-shortening cycle; youth; maturation; SSC potentiation; countermovement jump; squat jump

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