Abstract
Objectives
The purpose of this study was to compare the duration of high-intensity static stretching on flexibility and strength in the hamstrings.
Methods
Fourteen healthy males (20.8 ± 0.6 years, 170.7 ± 6.5 cm, 66.4 ± 9.9 kg) underwent high-intensity static stretching for three different durations (10, 15, and 20 seconds). The intensity of static stretching was set at the maximum point of discomfort. To examine the change in flexibility and strength, range of motion, peak passive torque, relative passive torque, muscle-tendon unit stiffness, peak torque of isokinetic knee flexion, and knee angle at peak torque of isokinetic knee flexion were measured. To evaluate a time course of pain, a numerical rating scale was described.
Results
Range of motion (P < 0.01), peak passive torque (P < 0.01), and knee angle at peak torque were increased at all interventions. Relative passive torque (P < 0.01) and muscle-tendon unit stiffness (P < 0.01) were decreased at all interventions. Peak torque decreased after 10 seconds of stretching (P < 0.05). Numerical rating scale during stretching was 8–9 levels in all interventions, the pain disappeared immediately after the post-measurements (median = 0).
Conclusion
The results suggested that muscle-tendon unit stiffness decreased regardless of duration of high-intensity static stretching. However, peak torque of isokinetic knee flexion decreased after 10 seconds of high-intensity static stretching, though it was no change after for more than 15 seconds of stretching.
Introduction
Static stretching (SS) is commonly used as a part of a warm-up routine in order to increase range of motion (ROM) and potentially prevent injuries [1]. Previous review studies reported that SS increases ROM effectively [2–5]. However, it is pointed out that the passive property of the muscle-tendon unit and tolerance for stretching influences ROM [5–7]. The passive property of the muscle-tendon unit is measured by using muscle-tendon unit stiffness, which is calculated from the slope of the torque-angle curve during passive joint movement [8–10]. On the other hand, tolerance for stretching is measured by peak passive torque during passive joint movement [10–12]. ROM is defined as one at which the subject is able to have a maximally tolerable angle without pain. An increase in the passive torque during the passive joint movement indicated that the subjects received higher force without pain, which indicates that an increase of tolerance is obtained.
Previous studies reported that muscle-tendon unit stiffness is related to the occurrence of muscle-tendon injuries [13–15]. Witvrouw et al. [16] suggested that a sufficient level of muscle-tendon unit compliance is needed for sports utilizing a stretch-shortening cycle to effectively store and release a high amount of elastic energy. In the case of insufficient muscle-tendon unit compliance, the demands in energy absorption and release may rapidly exceed the capacity of the muscle-tendon unit, which may cause a higher risk of injuries [6,17,18]. Many previous studies reported that SS decrease muscle-tendon unit stiffness effectively [7,19,20]. Therefore, SS used as a part of warm-up routine decreases muscle-tendon unit stiffness and could lead to preventing injuries.
The effects of SS on muscle-tendon unit stiffness is affected by its duration [9,21] and intensity [7,8,22]. Matsuo et al. [9] and Nakamura et al. [21] examined the duration of SS needed to decrease muscle-tendon unit stiffness of hamstrings, and they showed that three minutes of SS was needed to decrease the stiffness. However, previous studies reported the duration of SS used as a part of a warm-up routine is approximately 20 seconds [1,23]. In fact, Takeuchi et al. [22] reported that 20 seconds of SS in hamstrings does not change muscle-tendon unit stiffness. Moreover, Sato et al. [24] examined the influence of SS for 20 seconds in gastrocnemius muscle on shear elastic modulus, which is an indicator as a passive property of the muscle measured by using shear wave elastography, and showed the shear elastic modulus did not change after the stretching. These data suggest that SS for 20 seconds used as a part of a warm-up routine does not change muscle-tendon unit stiffness and may not be able to prevent injury as well. However, because many athletes practice within a limited time, it is difficult to perform SS for more than 180 seconds for each muscle. Therefore, it is necessary to develop an SS that can decrease muscle-tendon unit stiffness in 20 seconds.
The influence of SS is affected by its intensity as well as its duration [8,22]. Kataura et al. [8] examined the effect of different intensities of SS and reported that there was a significant moderate negative correlation between the intensity of SS and relative change in passive stiffness. Moreover, our previous study examined high-intensity of SS for 20 seconds in hamstrings and showed that muscle-tendon unit stiffness decreased after the stretching [22]. However, SS at high intensity is accompanied by moderate to severe pain [8,22]. Our previous study measured the pain level by using a numerical rating scale [NRS; 11-point scale raged from 0 (no pain) to 10 (worst imaginable pain)] [22]. The results indicated that median of NRS during SS at high intensity was 8, although NRS immediately after the stretching and 24 hours after the stretching were both 0 levels [22]. To minimize the pain during SS at high intensity, it is important to examine the optimal duration of the stretching.
A previous study investigating static stretching protocol reported that SS for less than 10 seconds was rarely performed [1]. On the other hand, SS for 10 to 19 seconds was frequently used [1]. Therefore, the purpose of this study was to compare the duration of high-intensity SS (10, 15, and 20 seconds) on flexibility and strength in the hamstrings and to clarify the optimal duration of SS at high intensity.
Materials and methods
Participants
Fourteen healthy men (20.8 ± 0.6 years, 170.7 ± 6.5 cm, 66.4 ± 9.9 kg) were recruited. Participants who regularly performed any flexibility and strength training or who had a history of lower limb pathology were excluded. The sample size was calculated with a power of 80%, alpha error of 0.05, and effect size of 0.25 (middle) using G*Power 3.1 software (Heinrich Heine University, Düsseldorf, Germany), and the results showed that the requisite number of participants for this study was 14. All participants were informed of the requirements and risks associated with their involvement in this study and signed a written informed consent document. The study was performed in accordance with the Declaration of Helsinki (1964). The Ethics Committee of Kobe International University approved the study.
Procedure
The purpose of the present study was to examine the optimal duration of high-intensity SS in hamstrings. For this purpose, the participants underwent three different duration of high-intensity SS (10 sec, 15 sec, and 20 sec) in the right hamstrings, in random order. The participants visited three times on a separate day, with an interval of one week. Participants attended a familiarization session at least 24 hours before the first testing day. To evaluate any alteration of flexibility and strength of the right hamstrings, ROM, passive torque, peak torque during isokinetic knee flexion and knee angle at peak torque of isokinetic knee flexion were measured before and after each SS. In addition, NRS was examined during SS, immediately after the post-measurement, and 24 hours after SS. The experiment was performed in a university laboratory, where the temperature was maintained at 25 degrees C.
Flexibility assessment
The flexibility assessment was performed in the same fashion as a previous study [8,22]. The previous study reported that the reliability of the measurements used in this study was acceptable [8]. An isokinetic dynamometer machine (CYBEX NORM, Humac, California, USA) was used in the present study. This study used a sitting position in which the hip joint was flexed, which has been shown to efficiently stretch the hamstrings [8]. The participants were seated on a chair with the seat tilted maximally, and a wedge-shaped cushion was inserted between the trunk and the backrest, which set the angle between the seat and the back at approximately 60 degrees. The previous study, which used the same assessment, reported that the average angle of hip flexion was 111.2 ± 2.5 degrees [8]. The chest, pelvis, and right thigh were stabilized with straps. The right knee joint was aligned with the axis of the rotation of the isokinetic dynamometer machine. The lever arm attachment was placed just proximal to the malleolus medialis and stabilized with straps. In the present study, reported knee angles were measured using the isokinetic dynamometer machine. A 90-degree angle between the lever arm and floor was defined as 0 degrees of knee flexion/extension. The participants were instructed to relax during the flexibility assessment.
ROM
The knee joint was passively extended from 0 degrees to maximum angle without pain at 5 degrees/seconds. A previous study showed that the velocity does not cause stretch reflex [25]. ROM was defined as the range from 0 degrees to the maximum knee extension angle.
Passive torque
The passive torque during ROM measurement was recorded in the isokinetic dynamometer machine. Passive torque was obtained at two points [11]. (1) relative passive torque was obtained at the same knee angle reached before SS to examine changes in passive properties of the muscle-tendon unit. (2) Peak passive torque was obtained at maximum ROM both before and after SS to examine tolerance for stretching.
Calculation of muscle-tendon unit stiffness
Muscle-tendon unit stiffness was defined as the values of the slope of the regression line that was calculated from the torque-angle relationship using the least-squares method [10]. Muscle-tendon unit stiffness was calculated from the same knee extension angle range before and after SS. The calculated knee extension angle range was defined as the angle from the 50% maximum knee extension angle to the maximum knee extension angle measured before SS [8,9,22].
Peak torque and knee angle during maximum voluntary isokinetic knee flexion
The peak torque of knee flexion during maximum voluntary isokinetic knee flexion at 60 degrees/second was measured. The participants were secured on the isokinetic dynamometer machine in the same fashion as the measurement of ROM. The range of the measurement was set from 0 degrees to maximum knee extension angle. The participants performed three submaximal isokinetic knee flexion as a warm-up trial. After the warm-up trial, the participants performed three maximum isokinetic knee flexion as muscle strength measurement. The greatest values of three isokinetic knee flexion were used for the analyses as the peak torque. The joint angle at the peak torque was provided by the isokinetic dynamometer machine.
Numerical rating scale
The level of pain during SS, immediately after the post-measurement, and 24 hours after SS were quantified by an 11-point NRS that ranged from 0 (no pain) to 10 (worst imaginable pain) [8,22].
Static stretching
SS was performed on the isokinetic dynamometer machine in the same fashion as the measurement of ROM. The knee joint was passively extended from 0 degrees to the angle at the maximum point of discomfort [22]. The angle was held for three different duration (10 sec, 15 sec, and 20 sec). Thereafter, the knee joint was passively returned to 0 degrees. The participants received one set of stretching at each different duration. The participants were instructed to relax during each stretch. The percent change in angle during SS respect to ROM before the stretching was defined as the intensity of the stretching [8,22].
Statistical analyses
All variables except NRS were described as mean ± SD in the present study. NRS was described as a median. A one-way repeated measure analysis of variance was used to examine the difference in intensity of SS. For variables except for NRS, a two-way repeated measures analysis of variance was used to examine the effects of intervention (10 sec vs. 15 sec vs. 20 sec) and time (pre vs. post). For NRS, a two-way repeated-measures analysis of variance was used to examine the effects of intervention (10 sec vs. 15 sec vs. 20 sec) and time (during SS vs. immediately after the post-measurements vs. 24 hours after SS). If a significance was detected, post hoc analyses using Bonferroni’s test were performed. Spearman’s rank correlation coefficient was conducted between the intensity of SS and relative change of ROM, relative passive torque, peak passive torque, and muscle-tendon unit stiffness. The analyses were performed using SPSS version 25 (SPSS, Inc., Chicago, IL, USA). Differences were considered statistically significant at an alpha level of p < 0.05. To describe the effect size, the partial eta squared value was calculated by using the SPSS software.
Results
Intensity of SS
The intensity of SS for each intervention were as follows: 10 sec, 137.9 ± 11.4%; 15 sec, 128.9 ± 12.7%; 20 sec, 130.3 ± 8.6%. There was no significant difference in intensity of SS between interventions (p = 0.07, partial eta squared = 0.19).
ROM
For ROM, there was no significant two-way interaction (intervention × time, p = 0.12, partial eta squared = 0.10) and no main effect for intervention (p = 0.37, partial eta squared = 0.05), but there was significant main effect for time (p < 0.01, partial eta squared = 0.75) (Fig 1). ROM increased after the stretching (p < 0.01).
Relative passive torque
For relative passive torque, there was no significant two-way interaction (intervention × time, p = 0.63, partial eta squared = 0.02) and no main effect for intervention (p = 0.84, partial eta squared = 0.01), but there was significant main effect for time (p < 0.01, partial eta squared = 0.86) (Fig 1). Relative passive torque decreased after each SS (p < 0.01).
Peak passive torque
For peak passive torque, there was no significant two-way interaction (intervention × time, p = 0.42, partial eta squared = 0.04) and no main effect for intervention (p = 0.49, partial eta squared = 0.04), but there was significant main effect for time (p < 0.01, partial eta squared = 0.22) (Fig 1). Peak passive torque increased after the stretching (p < 0.01).
Muscle-tendon unit stiffness
For muscle-tendon unit stiffness, there was no significant two-way interaction (intervention × time, p = 0.62, partial eta squared = 0.02) and no main effect for intervention (p = 0.78, partial eta squared = 0.01), but there was significant main effect for time (p < 0.01, partial eta squared = 0.84) (Fig 1). Muscle-tendon unit stiffness decreased after the stretching (p < 0.01).
Peak torque of isokinetic knee flexion
For peak torque of isokinetic knee flexion, there was significant two-way interaction (intervention × time, p < 0.05, partial eta squared = 0.15) (Fig 2). Post hoc analysis revealed that the peak torque decreased after 10 sec of SS (p < 0.05) while there was no change after 15 and 20 sec of SS (p = 0.96, 0.30, respectively).
Knee angle at peak torque of isokinetic knee flexion
For knee angle at peak torque of isokinetic knee flexion, there was no significant two-way interaction (intervention × time, p = 0.42, partial eta squared = 0.04) and no main effect for intervention (p = 0.52, partial eta squared = 0.03), but there was significant main effect for time (p < 0.01, partial eta squared = 0.52) (Fig 2). The knee angle increased after the stretching (p < 0.01).
NRS
For NRS, there was no significant two-way interaction (intervention × time, p = 0.54, partial eta squared = 0.04) and no main effect for intervention (p = 0.72, partial eta squared = 0.02), but there was significant main effect for time (p < 0.01, partial eta squared = 0.98). NRS during SS [median values (interquartile range):10 sec = 9 (8–9), 15 sec = 8 (8–9), 20 sec = 8 (8–9)] indicated higher values compared with those immediately after the post-measurements [median values (interquartile range): 0 (0 = 0) in all interventions] (p < 0.01) and 24 hours after SS [median values (interquartile range): 0 (0 = 0) in all interventions] (p < 0.01).
Correlation between intensity and measurements of flexibility
There was significant correlations between intensity of SS and the relative change in ROM (10 sec, r = 0.88, p < 0.01; 15 sec, r = 0.94, p < 0.01; 20 sec; r = 0.52, p < 0.05), relative passive torque (10 sec, r = -0.62, p < 0.05; 15 sec, r = -0.78, p < 0.01; 20 sec, r = -0.72, p < 0.01), and muscle-tendon unit stiffness (10 sec, r = -0.61, p < 0.05; 15 sec, r = -0.74, p < 0.01; 20 sec, r = -0.62, p < 0.05). On the other hand, there was no significant correlations between intensity of SS and relative change in peak passive torque (10 sec, r = 0.51, p = 0.07; 15 sec, r = 0.29, p = 0.32; 20 sec, r = 0.14, p = 0.63).
Discussion
In this study, SS was performed at the angle where the maximum point of discomfort. The results showed that there was no significant difference in the intensity of SS between interventions. In addition, there was no significant difference in NRR during SS between interventions. These results indicated that the participants received SS at similar intensity subjectively and objectively regardless of the duration of SS.
In the present study, regardless of the interventions, ROM and peak passive torque significantly increased but relative passive torque and muscle-tendon unit stiffness significantly decreased. Alteration in ROM after SS are attributed to alterations in passive property of the muscle and tolerance for stretching [5–7]. In the present study, relative passive torque [11] and muscle-tendon unit stiffness [7,10,19] were measured as indicators of the passive property of the hamstrings, and peak passive torque was measured as an indicator of tolerance for stretching [10,26,27]. Previous studies showed that ROM and peak passive torque increased, but muscle-tendon unit stiffness of the hamstrings decreased after high-intensity SS for 20 [22] and 180 seconds [8]. These results suggested that the effects of the duration of high-intensity SS was small, and the stretching increased ROM through a decrease in relative passive torque and muscle-tendon unit stiffness and an increase in tolerance for stretching.
In all interventions, there were significant correlations between the intensity of SS and relative changes in ROM, relative passive torque, and muscle-tendon unit stiffness. However, there were no significant correlations between the intensity of SS and peak passive torque. Our previous study examined the effects of high-intensity SS for 20 seconds and showed that there were significant correlations between the intensity of SS and ROM, muscle-tendon unit stiffness, and peak passive torque [22]. While, Kataura et al. [8] examined the effect of high intensity of SS for 180 seconds in hamstrings and reported that there were significant correlations between the intensity of SS and ROM and passive stiffness, though there was no significant correlation between the intensity of SS and peak passive torque. From these three studies, when the high-intensity SS is performed, it is suggested that the intensity of SS is important for the change in ROM and passive property of the hamstrings. On the other hand, no consensus has been obtained regarding the relationship between the intensity of SS and changes in tolerance for stretching. Although the details of the mechanisms for the increase in tolerance for stretching are unclear, previous studies have reported that the increase in stretch tolerance was attributed to decrement in the perceptions of pain and discomfort accompanied by a change of neural and psychological factors after stretching [28,29]. Previous studies reported that change in ROM after SS at the intensity of no pain is more affected by stretch tolerance than passive properties [30,31]. The change in tolerance for stretching after high-intensity SS needs to be studied in more detail.
In the present study, the peak torque of isokinetic knee flexion was decreased after SS for 10 seconds, while it was no change after SS for 15 and 20 seconds. In our previous study, the peak torque was not changed after high-intensity SS for 20 seconds [22], and in this regard, the results of the present study support the previous study. The alteration in muscle strength after SS is attributed to an alteration in muscle-tendon unit stiffness [32,33] and neural activity [34–37]. SS theoretically decreases the force transfer efficiency from the muscle to the skeleton [38] with the decrement in muscle-tendon unit stiffness [32,33] and rightward shift of torque-angle curve [39–41]. Trajano et al. [35] reported that central factors were strongly related to the torque reduction immediately after SS and during torque recovery. In the present study, decrement in muscle-tendon stiffness and increment in knee angle at peak torque of isokinetic knee flexion were found regardless of its duration. Increment in the knee angle at peak torque indicated a rightward shift of torque angle curve [41]. Therefore, it is suggested that the difference in peak torque of isokinetic knee flexion was caused by neural activity because there were no differences in changes in muscle-tendon unit stiffness and knee angle at peak torque between interventions.
Previous studies reported that sympathetic nerve activity is activated following pain and discomfort levels [42,43]. The sympathetic nerve plays a crucial role in blood flow and neural activity during muscle contraction [44]. In the present study, NRS during SS was 8–9 levels in all interventions, which indicated that the participants felt severe pain. To our best knowledge, it has not been examined to the extent of stretching stimulation required for sympathetic nerve excitation. However, it is possible that 10 seconds of high-intensity SS was insufficient for sympathetic nerve excitation, and the sympathetic nerve excitation required for more than 15 seconds of the stretching. Therefore, it is suggested that the peak torque of isokinetic knee flexion was decreased because of the decrement in muscle-tendon unit stiffness after 10 seconds of high-intensity SS. while the effect of the decrement in the stiffness would be offset by an increment in sympathetic nerve activity after 15 and 20 seconds of the stretching. However, the present study did not measure sympathetic nerve activity. In addition, EMG activity of the hamstrings could not be measured because the right thigh was stabilized to the seat with a strap in order to accurately perform measurements and interventions. It is necessary to examine the changes in neural activity after high-intensity SS in detail in order to clarify the mechanism of change in the peak torque of isokinetic knee flexion after the stretching.
In the present study, NRS was 8–9 levels during SS, which indicated that participants felt severe pain. However, the pain was disappeared immediately after the post-measurements, and there was no pain 24 hours after SS. These results are consistent with our previous study [22]. These data suggested that risk of high-intensity SS may be low for healthy men. However, Apostolopoulos [45] compared the effects of high- (70%-80% maximum perceived stretch) and low-intensity (30%-40% maximum perceived stretch) SS on recovery from unaccustomed eccentric exercise. They showed that low-intensity stretching is likely to result in small-to-moderate beneficial effects on perceived muscle soreness and recovery of muscle function post-unaccustomed eccentric exercise [45]. Therefore, it is necessary to investigate the safety of high-intensity SS for the persons with muscle-tendon disorders.
In summary, the results showed that muscle-tendon unit stiffness decreased regardless of its duration. However, peak torque of isokinetic knee flexion, which is an indicator of muscle strength of the hamstrings, decreased after high-intensity SS for 10 seconds, although there was no change after more than 15 seconds of high-intensity SS. The decrement in muscle strength after SS is restored within 10 minutes [33]. Moreover, performing activities (jumps and sprints) following SS can mitigate the negative effects of SS [46,47]. These data suggested that if athletes elect to stretch statically, they need to choose the duration of high-intensity SS taking into account their subsequent activities. Athletes who need great muscle strength immediately after high-intensity SS without any activities should use more than 15 seconds of stretching. If athletes have more than 10 minutes or perform activities after high-intensity SS, they should use 10 seconds of high-intensity SS to minimize the pain.
Conclusions
The present study showed that, regardless of the duration of SS, ROM and peak passive torque increased, but relative passive torque and muscle-tendon unit stiffness decreased. Peak torque of isokinetic knee flexion decreased after 10 seconds of high-intensity SS. High-intensity SS for 10 seconds could be useful to increase flexibility and prevent injuries. However, athletes should use high-intensity SS for more than 15 seconds when they need great muscle strength immediately after stretching.
Supporting information
Data Availability
All relevant data are within the manuscript and its Supporting Information files.
Funding Statement
The authors received no specific funding for this work.
References
- 1.Takeuchi K, Nakamura M, Kakihana H, Tsukuda F. A Survey of static and dynamic stretching protocol. Int J Sport Heal Sci. 2019;17: 72–79. 10.5432/ijshs.201829 [DOI] [Google Scholar]
- 2.Radford JA, Burns J, Buchbinder R, Landorf KB, Cook C. Does stretching increase ankle dorsiflexion range of motion? A systematic review. Br J Sports Med. 2006;40: 870–5; discussion 875. 10.1136/bjsm.2006.029348 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Nakano J, Yamabayashi C, Scott A, Reid WD. The effect of heat applied with stretch to increase range of motion: A systematic review. Phys Ther Sport. 2012;13: 180–188. 10.1016/j.ptsp.2011.11.003 [DOI] [PubMed] [Google Scholar]
- 4.Medeiros DM, Cini A, Sbruzzi G, Lima CS. Influence of static stretching on hamstring flexibility in healthy young adults: Systematic review and meta-analysis. Physiotherapy Theory and Practice. Taylor and Francis Ltd; 2016. pp. 438–445. 10.1080/09593985.2016.1204401 [DOI] [PubMed] [Google Scholar]
- 5.Behm DG, Blazevich AJ, Kay AD, McHugh M. Acute effects of muscle stretching on physical performance, range of motion, and injury incidence in healthy active individuals: A systematic review. Applied Physiology, Nutrition and Metabolism. National Research Council of Canada; 2016. pp. 1–11. 10.1139/apnm-2015-0235 [DOI] [PubMed] [Google Scholar]
- 6.Magnusson SP, Simonsen EB, Aagaard P, Boesen J, Johannsen F, Kjaer M. Determinants of musculoskeletal flexibility: viscoelastic properties, cross-sectional area, EMG and stretch tolerance. Scand J Med Sci Sports. 1997;7: 195–202. 10.1111/j.1600-0838.1997.tb00139.x [DOI] [PubMed] [Google Scholar]
- 7.Nakamura M, Ikezoe T, Takeno Y, Ichihashi N. Time course of changes in passive properties of the gastrocnemius muscle-tendon unit during 5 min of static stretching. Man Ther. 2013;18: 211–215. 10.1016/j.math.2012.09.010 [DOI] [PubMed] [Google Scholar]
- 8.Kataura S, Suzuki S, Matsuo S, Hatano G, Iwata M, Yokoi K, et al. Acute Effects of the Different Intensity of Static Stretching on Flexibility and Isometric Muscle Force. J strength Cond Res. 2017;31: 3403–3410. 10.1519/JSC.0000000000001752 [DOI] [PubMed] [Google Scholar]
- 9.Matsuo S, Suzuki S, Iwata M, Banno Y, Asai Y, Tsuchida W, et al. Acute Effects of Different Stretching Durations on Passive Torque, Mobility, and Isometric Muscle Force. J Strength Cond Res. 2013;27: 3367–3376. 10.1519/JSC.0b013e318290c26f [DOI] [PubMed] [Google Scholar]
- 10.Magnusson SP, Simonsen EB, Aagaard P, Soørensen H, Kjær M. A mechanism for altered flexibility in human skeletal muscle. J Physiol. 1996;497: 291–298. 10.1113/jphysiol.1996.sp021768 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Brusco CM, Blazevich AJ, Pinto RS. The effects of 6 weeks of constant-angle muscle stretching training on flexibility and muscle function in men with limited hamstrings’ flexibility. Eur J Appl Physiol. 2019;119: 1691–1700. 10.1007/s00421-019-04159-w [DOI] [PubMed] [Google Scholar]
- 12.Medeiros DM, Martini TF. Chronic effect of different types of stretching on ankle dorsiflexion range of motion: Systematic review and meta-analysis. Foot. Churchill Livingstone; 2018. pp. 28–35. 10.1016/j.foot.2017.09.006 [DOI] [PubMed] [Google Scholar]
- 13.Ekstrand J, Gillquist J. The avoidability of soccer injuries. Int J Sports Med. 1983;4: 124–128. 10.1055/s-2008-1026025 [DOI] [PubMed] [Google Scholar]
- 14.Pickering Rodriguez EC, Watsford ML, Bower RG, Murphy AJ. The relationship between lower body stiffness and injury incidence in female netballers. Sport Biomech. 2017;16: 361–373. 10.1080/14763141.2017.1319970 [DOI] [PubMed] [Google Scholar]
- 15.Watsford ML, Murphy AJ, McLachlan KA, Bryant AL, Cameron ML, Crossley KM, et al. A prospective study of the relationship between lower body stiffness and hamstring injury in professional Australian rules footballers. Am J Sports Med. 2010;38: 2058–2064. 10.1177/0363546510370197 [DOI] [PubMed] [Google Scholar]
- 16.Witvrouw E, Mahieu N, Danneels L, McNair P. Stretching and injury prevention: An obscure relationship. Sports Medicine. 2004. pp. 443–449. 10.2165/00007256-200434070-00003 [DOI] [PubMed] [Google Scholar]
- 17.Brazier J, Maloney S, Bishop C, Read PJ, Turner AN. Lower Extremity Stiffness: Considerations for Testing, Performance Enhancement, and Injury Risk. J Strength Cond Res. 2019;33: 1156–1166. 10.1519/JSC.0000000000002283 [DOI] [PubMed] [Google Scholar]
- 18.Lorimer A V., Hume PA. Stiffness as a Risk Factor for Achilles Tendon Injury in Running Athletes. Sports Medicine. Springer International Publishing; 2016. pp. 1921–1938. 10.1007/s40279-016-0526-9 [DOI] [PubMed] [Google Scholar]
- 19.Mizuno T, Matsumoto M, Umemura Y. Decrements in stiffness are restored within 10 min. Int J Sports Med. 2013;34: 484–490. 10.1055/s-0032-1327655 [DOI] [PubMed] [Google Scholar]
- 20.Morse CI, Degens H, Seynnes OR, Maganaris CN, Jones DA. The acute effect of stretching on the passive stiffness of the human gastrocnemius muscle tendon unit. J Physiol. 2008;586: 97–106. 10.1113/jphysiol.2007.140434 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Nakamura M, Tome I, Nishishita S, Tanaka H, Umehara J, Ichihashi N. Static stretching duration needed to decrease passive stiffness of hamstring muscle-tendon unit. J Phys Fit Sport Med. 2019;8: 113–116. 10.7600/jpfsm.8.113 [DOI] [Google Scholar]
- 22.Takeuchi K, Nakamura M. Influence of High Intensity 20-Second Static Stretching on the Flexibility and Strength of Hamstrings. J Sports Sci Med. 2020;19: 429–435. [PMC free article] [PubMed] [Google Scholar]
- 23.Simenz CJ, Dugan CA, Ebben WP. Strength and Conditioning Practices of National Basketball Association Strength and Conditioning Coaches. J Strength Cond Res. 2005;19: 495–504. 10.1519/15264.1 [DOI] [PubMed] [Google Scholar]
- 24.Sato S, Kiyono R, Takahashi N, Yoshida T, Takeuchi K, Nakamura M. The acute and prolonged effects of 20-s static stretching on muscle strength and shear elastic modulus. PLoS One. 2020;15 10.1371/journal.pone.0228583 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Morse CI. Gender differences in the passive stiffness of the human gastrocnemius muscle during stretch. Eur J Appl Physiol. 2011;111: 2149–2154. 10.1007/s00421-011-1845-z [DOI] [PubMed] [Google Scholar]
- 26.Mizuno T, Matsumoto M, Umemura Y. Viscoelasticity of the muscle-tendon unit is returned more rapidly than range of motion after stretching. Scand J Med Sci Sports. 2013;23: 23–30. 10.1111/j.1600-0838.2011.01329.x [DOI] [PubMed] [Google Scholar]
- 27.Kay AD, Blazevich AJ. Moderate-duration static stretch reduces active and passive plantar flexor moment but not Achilles tendon stiffness or active muscle length. J Appl Physiol. 2009;106: 1249–1256. 10.1152/japplphysiol.91476.2008 [DOI] [PubMed] [Google Scholar]
- 28.Law RYW, Harvey LA, Nicholas MK, Tonkin L, De Sousa M, Finniss DG. Stretch exercises increase tolerance to stretch in patients with chronic musculoskeletal pain: a randomized controlled trial. Phys Ther. 2009;89: 1016–26. 10.2522/ptj.20090056 [DOI] [PubMed] [Google Scholar]
- 29.Folpp H, Deall S, Harvey LA, Gwinn T. Can apparent increases in muscle extensibility with regular stretch be explained by changes in tolerance to stretch? Aust J Physiother. 2006;52: 45–50. 10.1016/s0004-9514(06)70061-7 [DOI] [PubMed] [Google Scholar]
- 30.Magnusson SP. Passive properties of human skeletal muscle during stretch maneuvers. A review. Scand J Med Sci Sports. 1998;8: 65–77. 10.1111/j.1600-0838.1998.tb00171.x [DOI] [PubMed] [Google Scholar]
- 31.Freitas SR, Mendes B, Le Sant G, Andrade RJ, Nordez A, Milanovic Z. Can chronic stretching change the muscle-tendon mechanical properties? A review. Scand J Med Sci Sport. 2018;28: 794–806. 10.1111/sms.12957 [DOI] [PubMed] [Google Scholar]
- 32.Fowles JR, Sale DG, MacDougall JD. Reduced strength after passive stretch of the human plantarflexors. J Appl Physiol. 2000;89: 1179–1188. 10.1152/jappl.2000.89.3.1179 [DOI] [PubMed] [Google Scholar]
- 33.Mizuno T, Matsumoto M, Umemura Y. Stretching-induced deficit of maximal isometric torque is restored within 10 minutes. J strength Cond Res. 2014;28: 147–153. 10.1519/JSC.0b013e3182964220 [DOI] [PubMed] [Google Scholar]
- 34.Behm DG, Chaouachi A. A review of the acute effects of static and dynamic stretching on performance. Eur J Appl Physiol. 2011;111: 2633–2651. 10.1007/s00421-011-1879-2 [DOI] [PubMed] [Google Scholar]
- 35.Trajano GS, Seitz L, Nosaka K, Blazevich AJ. Contribution of central vs. peripheral factors to the force loss induced by passive stretch of the human plantar flexors. J Appl Physiol. 2013;115: 212–8. 10.1152/japplphysiol.00333.2013 [DOI] [PubMed] [Google Scholar]
- 36.Trajano GS, Seitz LB, Nosaka K, Blazevich AJ. Can passive stretch inhibit motoneuron facilitation in the human plantar flexors? J Appl Physiol. 2014;117: 1486–1492. 10.1152/japplphysiol.00809.2014 [DOI] [PubMed] [Google Scholar]
- 37.Trajano GS, Nosaka K, Blazevich AJ. Neurophysiological Mechanisms Underpinning Stretch-Induced Force Loss. Sports Med. 2017;47: 1531–1541. 10.1007/s40279-017-0682-6 [DOI] [PubMed] [Google Scholar]
- 38.Huijing PA. Muscle as a collagen fiber reinforced composite: A review of force transmission in muscle and whole limb. J Biomech. 1999;32: 329–345. 10.1016/s0021-9290(98)00186-9 [DOI] [PubMed] [Google Scholar]
- 39.Balle SS, Magnusson SP, McHugh MP. Effects of contract-relax vs static stretching on stretch-induced strength loss and length-tension relationship. Scand J Med Sci Sports. 2015;25: 764–9. 10.1111/sms.12399 [DOI] [PubMed] [Google Scholar]
- 40.Avela J, Finni T, Liikavainio T, Niemelä E, Komi P V. Neural and mechanical responses of the triceps surae muscle group after 1 h of repeated fast passive stretches. J Appl Physiol. 2004;96: 2325–2332. 10.1152/japplphysiol.01010.2003 [DOI] [PubMed] [Google Scholar]
- 41.Weir DE, Tingley J, Elder GCBB. Acute passive stretching alters the mechanical properties of human plantar flexors and the optimal angle for maximal voluntary contraction. Eur J Appl Physiol. 2005;93: 614–23. 10.1007/s00421-004-1265-4 [DOI] [PubMed] [Google Scholar]
- 42.Matsubara T, Arai YCP, Shiro Y, Shimo K, Nishihara M, Sato J, et al. Comparative effects of acupressure at local and distal acupuncture points on pain conditions and autonomic function in females with chronic neck pain. Evidence-based Complement Altern Med. 2011;2011 10.1155/2011/543291 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Shiro Y, Arai Y-CP, Matsubara T, Isogai S, Ushida T. Effect of muscle load tasks with maximal isometric contractions on oxygenation of the trapezius muscle and sympathetic nervous activity in females with chronic neck and shoulder pain. BMC Musculoskelet Disord. 2012;13: 146 10.1186/1471-2474-13-146 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Katayama K, Saito M. Muscle sympathetic nerve activity during exercise. J Physiol Sci. 2019;69 10.1007/s12576-019-00669-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Apostolopoulos NC, Lahart IM, Plyley MJ, Taunton J, Nevill AM, Koutedakis Y, et al. The effects of different passive static stretching intensities on recovery from unaccustomed eccentric exercise—A randomized controlled trial. Appl Physiol Nutr Metab. 2018;43: 806–815. 10.1139/apnm-2017-0841 [DOI] [PubMed] [Google Scholar]
- 46.Samson M, Button DC, Chaouachi A, Behm DG. Effects of dynamic and static stretching within general and activity specific warm-up protocols. J Sport Sci Med. 2012;11: 279–285. [PMC free article] [PubMed] [Google Scholar]
- 47.Chaabene H, Behm DG, Negra Y, Granacher U. Acute Effects of Static Stretching on Muscle Strength and Power: An Attempt to Clarify Previous Caveats. Front Physiol. 2019;10: 1468 10.3389/fphys.2019.01468 [DOI] [PMC free article] [PubMed] [Google Scholar]