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Regular stretch does not increase muscle extensibility: a randomized controlled trial
M. Ben1,2, L. A Harvey1,2
Rehabilitation Studies Unit, Northern Clinical School, Faculty of Medicine, University of Sydney, Sydney, Australia, 2Physiotherapy Department, Royal Rehabilitation Centre Sydney, Sydney, Australia
1
Corresponding author: Dr Lisa Harvey, Rehabilitation Studies Unit, University of Sydney, PO Box 6, Ryde, NSW, Australia 1680. E-mail: l.harvey@usyd.edu.au
Accepted for publication 8 January 2009
The purpose of this randomized controlled trial was to determine whether regular stretch increases hamstring muscle extensibility. Sixty healthy individuals were randomly allocated to an experimental or a control group. The experimental group attended supervised stretch sessions where they stretched the hamstring muscles of a randomly allocated leg for 30 min ve times a week for 6 weeks. The control group did not attend any stretch sessions during this period. No participants withdrew from the study. A purpose built device was used to measure passive hip exion during a straight leg-raise manoeuvre with the application of a standardized and non-standardized stretch torque. The
stretch intervention did not increase passive hip exion when measured with a standardized stretch torque [mean treatment eect 5 11; 95% condence interval (CI) 5 3 to 21]. It did, however, increase passive hip exion when measured without a standardized stretch torque (mean treatment eect 5 101, 95% CI 5 6141). Six weeks of sustained 30-min daily stretch does not increase the extensibility of the hamstring muscle of healthy individuals. It does, however, improve stretch tolerance leading to increased joint range of motion without any actual improvements in muscle extensibility.
Stretches are routinely incorporated into physical training programs (Bandy & Irion, 1994; Bandy et al., 1997, 1998; Chan et al., 2001; Gajdosik et al., 2005). There is good evidence from animal studies to support the widespread use of stretch. These studies indicate that the muscles of rabbits, cats, guinea pigs and rats are adaptable and remodel in response to prolonged sustained stretch (Tabary et al., 1972; Tardieu et al., 1977; Huet de laTour et al., 1979; Spector et al., 1982; Herbert & Balnave, 1993). In these studies, stretch is typically administered continuously through the application of plaster casts for days and even weeks, although in one notable study stretch was administered for as little as 15 min a day (Williams, 1990). These studies indicate that sustained stretch increases the number of sarcomeres in series and stimulates rearrangement of collagen (Goldspink et al., 1974; Huet de laTour et al., 1979). These changes demonstrate the adaptable nature of muscle tissue necessary for optimal force production and usually reverse once the stimulus is removed (Timson, 1990). Associated with the structural and morphological adaptations are changes in the passive mechanical properties of muscles, notably changes in extensibility (Tabary et al., 1972; Goldspink et al., 1974). Changes in muscle extensibility are reected
by changes in joint angle with the application of a standardized torque. It is not clear whether the muscles of humans respond similarly to the muscles of small animals to the application of continuous sustained stretch. Several studies on humans provide initial evidence about the eectiveness of stretch (Gajdosik, 1991; Lentell et al., 1992; Bandy & Irion, 1994; Bandy et al., 1997, 1998; Chan et al., 2001; Draper et al., 2004; Gajdosik et al., 2005). Interestingly, unlike the animal trials, the majority of studies in humans administer stretch for as little as 30 s a day. However, these ndings need to be interpreted with caution. Often changes in extensibility are measured immediately upon removal of stretch and may primarily reect viscoelastic deformation (Bohannon, 1984; Kirsch et al., 1995; Magnusson et al., 1996c). These studies do not provide evidence about the lasting eects of stretch. In addition, the majority of trials in this area do not blind assessors nor adhere to the design features of clinical trials important for minimizing bias (Schulz et al., 1995; Schulz & Grimes, 2006). Perhaps of more concern though is the failure of trials to measure joint angle with a known torque (Starring et al., 1988; Godges et al., 1993; Bandy & Irion, 1994; Bandy et al., 1997). It is important to
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Study design
A single-blind randomized controlled trial using a combination of a within- and between-subjects design was undertaken. The participants were randomly allocated to a control or experimental group (between-subject component of the trial). Participants in the control group received no stretch intervention to either leg. Those in the experimental group, however, had each of their legs further randomized to either a stretch or nonstretch group (within-subject component of the trial). Thus, three groups were formed which for simplicity will be referred to as (i) control group, (ii) experimental-stretch group and (iii) experimental-non-stretch group (see Fig. 1). A computer-generated randomization schedule was produced by a person independent of the study. The allocation was concealed by sequentially numbered opaque envelopes which were opened by the principal investigator following initial measurements. Participants were considered to have entered the trial at this point. The within-subject component of the trial examined the eectiveness of stretch on passive hip exion with and without a standardized stretch torque. Each subject acted as their own control thereby minimizing between-group variability due to personal factors such as sport participation. However, a limitation of a within-subject design is that it does not account for the possibility of contralateral treatment eects. That is, stretch applied to one leg may increase passive hip exion in the untreated contralateral leg. In this scenario, a within-subjects design would fail to detect a treatment eect because both legs would improve with the intervention. The between-subject component of the trial was used to check for this possibility.
Outcome measures
The two primary outcome measures were passive hip exion with and without the application of a standardized hip exor torque. The standardized torque was 18 Nm and was selected because it was the largest torque all participants were likely to
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Baseline measurements
BETWEEN-SUBJECT COMPONENT
WITHIN-SUBJECT COMPONENT
tolerate (Folpp et al., 2006). It was important to select a torque that all participants could tolerate so results between participants could be compared. The non-standardized torque was determined by participants. That is, passive hip exion was measured with the highest torque participants were willing to tolerate as is commonly done in clinical practice and clinical trials (Halbertsma et al., 1996; Magnusson et al., 1996b; Folpp et al., 2006). The secondary outcome measure was pain intensity at the point of the highest tolerated stretch torque and was used to determine participants perceptions of discomfort. Participants were asked to rate their pain on an 11-point visual analogue scale (VAS), with zero indicating no pain and ten indicating the worst possible pain (Bijur et al., 2001). Passive hip exion was measured during a straight leg raise manoeuvre with a device previously described and tested for reliability (ICC 5 0.98; see Fig. 2) (Harvey et al., 2003b). The device has three important features, namely it provides a way of stabilizing the knee in extension, ensures the hip moves in a sagittal plane and provides a way of quantifying the applied hip exor torque. Furthermore, the device negates the torque due to the mass of the leg by a counterweight system. In this way, the applied hip exor torque is solely directed at stretching the hamstring muscles and not inuenced by the mass of a participants leg.
Measurement procedure
Assessors, blinded to group allocation, tested the participants on two occasions at a physiotherapy gymnasium within a
Sydney hospital. Initial measurements were taken 17 days before the beginning of the study. The nal measurements were taken at the completion of the 6-week study period. All experimental participants were tested at least 24 h and not more than 4 days (mean 5 2 days, SD 5 1 day) after the last stretch intervention. This was important for ensuring measurements reected the lasting and not transient eects of the stretch intervention. Measurement procedures always followed the same protocol. Participants were prevented from seeing their legs during testing by a screen placed across their chests. This helped ensure that participants responded to sensation rather than visual cues of leg position. The right leg was measured before the left leg. Initially a standardized hip exor torque of 18 Nm was applied for 3 min to exhaust viscoelastic tissue deformation (Bohannon, 1984; Kirsch et al., 1995; Magnusson et al., 1996c). Following measurements with the standardized 18 Nm torque, passive hip exion was again measured but with a non-standardized torque. For this part of the test, the stretch torque was increased from the original 18 Nm by 6 Nm increments every 30 s. However, between each 6 Nm increment, small random increases and decreases in torque were applied. These were included to minimize participants ability to predict the testing protocol. Once participants indicated that they were not willing to tolerate further increases in torque, the last 6 Nm increment was removed and the torque was increased by 1.5 Nm every 10 s. Participants were again requested to indicate when they had reached their maximal stretch tolerance at which point passive hip exion and the
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Fig. 2. Device used to assess passive hip exion with and without a standardized stretch torque. A wheel with an attached leg splint (S) was secured to the side of the bed. Weights (W) were hung from the rim of the wheel to produce a hip exion torque. The torque due to weight of the splinted leg was eliminated by using a counterweight (CW) (image reproduced with permission from http://www.physiothera pyexercises.com.au).
Results No participants withdrew from the study. The protocol dictated that participants receive 30 stretch interventions over 42 days and that at least 18 of the 30 stretch interventions be supervised. The overall compliance was excellent and the participants received a mean of 29 stretch interventions (SD 5 2) over 41 days (SD 5 9). An average of 24 stretches interventions (SD 5 5) were supervised, and 5 (SD 5 3) were unsupervised for each participant. Participants characteristics are provided in Table 1. There were no statistically signicant between group dierences in passive hip exion with or without a standardized torque at the beginning of the trial (Tables 2 and 3; Figs 3 and 4). Several participants from each group were involved in regular recreational or sporting activities such as walking, jogging, weight training, cycling and various team sports. The level of participation in sport was similar between groups with 23 of 30 participants regularly exercising in the control group, and 24 of 30 participants regularly exercising in the experimental group. The mean changes in passive hip exion angle and VAS scores measured with and without a standardized torque for the three groups are summarized in Tables 2 and 3. The within-subject analyses (Figs 3 and 4; Table 2) revealed that there was no between-group (i.e., between experimental-stretch and experimental-non-stretch
corresponding torque were recorded. At this point participants were also asked to rate intensity of their pain.
Intervention
Participants in the experimental group were required to stretch the hamstring muscles of the allocated leg continuously for 30 min a day, ve times a week for 6 weeks. At least three and often ve stretches were supervised by one of the study investigators. For this purpose, participants were required to attend a physiotherapy gymnasium within a hospital. The fourth and fth sessions were not always directly supervised. However, compliance with the stretch program was monitored with diaries to record the number of supervised and unsupervised sessions. Diaries were checked at each supervised stretching session. Stretches were self-administered by participants. They were instructed to sit on a chair in an upright position with their backs supported and one leg raised on a height-adjustable examination bed. The knee was extended and the height of the examination bed was adjusted by participants with a handheld electric control. Participants were encouraged to raise the bed as high as possible throughout each 30-min stretch session in order to induce the largest stretch they were willing to tolerate. If the participants became uncomfortable, they were instructed to lower the bed slightly to reduce the stretch, or reposition themselves in the chair. Torques applied during each stretch session were not measured or standardized, however this mimics clinical practice. Participants allocated
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Discussion Thirty minutes of sustained stretch administered daily for 6 weeks does not increase muscle extensibility in healthy, active, able-bodied individuals. It does, however, improve participants tolerance to the discomfort associated with stretch allowing them to tolerate larger stretch torques. There was no change in pain intensity scores at the point of highest tolerated torque for any group following the 6week trial period. This indicates that the stretch intervention did not simply enable participants to endure higher levels of pain. Rather, the stretch intervention enabled participants to tolerate higher levels of stretch torque for the same amount of perceived pain. The eects of the stretch intervention on tolerance are only evident in the treated leg with no improvements seen in the contralateral untreated leg. The failure to demonstrate a treatment eect on muscle extensibility cannot be explained by insucient subject numbers because the 95% CI is narrow (95% CI 5 3 to 21) and falls well short of the minimally worthwhile treatment eect (i.e. 51). Nor can the negative results be explained by poor compliance. Participants were directly supervised 80% of the time. Participants performed the remaining 20% of stretch sessions in their own time but
Table 1. Number of males and females and mean (SD) age (years), height (cm), weight (kg) and distance between ngers and oor in toetouch test (cm) of participants
Gender Males Females Age (years) Height (cm) Weight (kg) Toe-touch distance (cm) Participants involved in sport and recreational activities
35 168 74 5
Number of participants involved in regular sport and recreational activities is also included.
Table 2. Results of the within-subjects component of the study showing effects of stretch on muscle extensibility and stretch tolerance following the 6-week stretch program
Standardized torque (muscle extensibility) Hip exion angle (1) 53 (11) Non-standard torque (stretch tolerance) Hip exion angle (1) 86 (15) Highest tolerated torque (Nm) 54 (17) VAS score 7 (2)
3 to 2 614 515 01
Mean (SD) changes in hip flexion angle (1) with the application of a standardized and non-standardized torques are provided for the experimental -stretch and experimental-non-stretch groups. Mean (SD) change in highest tolerated torque (Nm) and in VAS scores is also provided for the two groups. *Mean and 95% CI data are rounded to the nearest integer. For this reason the 95% CIs do not appear to be perfectly symmetrical about the mean. CI, confidence interval; VAS, visual analogue scale.
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Standardized torque (muscle extensibility) Hip exion angle (1) 55 (15) Non-standard torque (stretch tolerance) Hip exion angle (1) 88 (14) Highest tolerated torque (Nm) 53 (18) VAS score 7 (2)
54 (11) 60 (13) 6 (8) 92 (15) 96 (16) 4 (7) 56 (16) 61 (19) 5 (11) 7 (2) 7 (2) 0(2)
5 to 3 8 to 0 10 to 2 1 to 1
Mean (SD) changes in hip flexion angle (1) with the application of a standardized and non-standardized torques are provided for the experimental-nonstretch and control groups. Mean (SD) change in highest tolerated torque (Nm) and in VAS scores is also provided for the two groups. *Mean and 95% CI data are rounded to the nearest integer. For this reason the 95% CIs do not appear to be perfectly symmetrical about the mean. CI, confidence interval; VAS, visual analogue scale.
exp-stretch
exp-non-stretch
control
Fig. 3. Mean (SD) dierences in hip exion angle with application of standardized torque for the experimentalstretch, experimental-non-stretch and control groups.
Fig. 4. Mean (SD) dierences in hip exion angle with application of non- standardized torque for the experimental-stretch, experimental-non-stretch and control groups.
compliance was monitored weekly with diaries by the investigators. Thus, compliance with the stretch program was excellent and probably better than what is typically achieved in the community setting. It is, however, possible that the failure to demonstrate a treatment eect reects the low torque used to test muscle extensibility. The low torque was used to ensure all participants would tolerate it and thereby enable between-group comparisons. However, the results may have been dierent if extensibility had been measured with a higher torque. Future studies could explore this possibility by restricting inclusion to those able to tolerate larger torques. The conclusions made from the results of this study are in stark contrast to the majority of previous studies in able-bodied individuals (Toft et al., 1989; Gajdosik, 1991; Bandy & Irion, 1994; Worrell et al., 1994; Bandy et al., 1997; Chan et al., 2001), which conclude that stretch administered for as little as 30 s a day increases muscle extensibility (Bandy & Irion,
1994; Bandy et al., 1997). This may merely reect a failure to standardize torque when measuring joint angle (Starring et al., 1988; Godges et al., 1993; Bandy & Irion, 1994; Bandy et al., 1997). That is, often joint angle is measured at what investigators deem to be end of range. However, end of range is commonly determined by participants feelings of discomfort at the time of testing and does not necessarily reect muscle extensibility. Studies reporting increases in end of range may therefore merely reect changes in participants willingness to tolerate discomfort. Several recent studies support this explanation and have highlighted the importance of making a distinction between stretch tolerance and muscle extensibility (Halbertsma et al., 1996; Magnusson et al., 1996a, b; Bjorklund et al., 2001; Folpp et al., 2006). The conicting results may be also be due to failure to use non-blinded assessors, a control group (Toft et al., 1989), and concealed allocation (Toft et al., 1989; Gajdosik, 1991; Lentell et al., 1992; Bandy et al., 1997; Chan et al., 2001;
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Acknowledgements
The Engineering Department of the Royal Rehabilitation Centre Sydney for assisting with the design of the testing device and for manufacturing the testing device.
References
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