- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05154110
Comparison of Two Techniques for Maintaining Range of Motion
October 11, 2022 updated by: Seyyada Tahniat Ali, Bahria University
Comparison of Static Stretching on Whole Body Vibration and Strength Training for Improving and Maintaining Hamstring Range of Motion
Flexibility is a measurable physical capacity considered a key component of physical fitness.
Poor flexibility is usually attributed to excessive tension exerted by the antagonist muscles of the movement and supported by weak scientific evidence, static stretching is considered as the most effective intervention in the promotion of muscle extensibility, in attempting to improve mobility.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Flexibility is a measurable physical capacity considered as a key component of physical fitness thereby contributing to the health and performance of joints and the musculoskeletal system.
In recent years, there has been increasing evidence that muscle weakness is a major factor behind reduced mobility.
Consequently, training muscle contractility is likely to improve mobility .
Regardless of terminology and of the quality of supporting evidence, stretching emerges as an intervention that elongates the tissues in attempting to improve mobility .
Shortening lengthens the tissue on two out of three axes, while stretching only lengthens the tissue on one axis out of three .
All training, including movement, is, by definition, training of shortening and stretching cycles (SSCs).
Ergo, resistance training is also, inherently, one way to elongate .
Strength training is an active, voluntary, dynamic form of stretching.
Indeed, strength training is dynamic stretching.
Often, strength training is performed against external resistances, but this is not mandatory.
Moreover, strength training has been shown to improve mobility in sedentary adults , .
Study Type
Interventional
Enrollment (Actual)
22
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Sindh
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Karachi, Sindh, Pakistan, 75500
- Seyyada Tahniat Ali
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 25 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Both male and female
- Age between 18-25
- Recreationally active individuals (all kind of sports, gym, and outdoor leisure activities)
Exclusion Criteria:
- Individuals with any physiological or pathological problem
- Older age individuals
- Individuals that had hamstring injury in past 6 months
- Individuals that had quadriceps injury in past 6 months
- Individuals that had any lower limb injury in past 6 months
- Individuals involved in any other studies.
- Individuals involved in other WBV related study.
- Sedentary lifestyle individuals
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: strength training group
the group will receive strength training
|
In second group, strength training will be done for 4 days per week for 4 days.
Subjects will have 5 minutes warm up.
In 1st week, the protocol will be Nordic hamstring curl (NHC) with bend (3 sets of 8 reps), Prone hamstrings curl (4 sets of 12 reps/leg), Physio-ball leg curl (3 sets of 8 reps), Glute bridge (2 sets of 50 s/leg).
In 2nd to 4th week, the protocol will be NHC with bend (3 sets of 12 reps) Prone hamstrings curl (3 sets of 14 reps/leg) Physio-ball leg curl (3 sets of 10 reps) Glute bridge (2 sets of 50 s/leg).
There will be 30 seconds rest between each set and 1 minute rest between each exercise .
Pre and post AROM and PROM will be measured.
Active hamstring ROM will be measured via active knee extension using a goniometer with the leg in 90° of hip flexion, with the opposite leg extended.
Passive ROM will be measured via clinician-assisted knee extension with the leg in 90° of hip flexion.
|
|
Experimental: whole body vibration stretching group
the group will receive stretching on whole-body vibration
|
SSubjects will be refrained from maximum-effort or new routines for exercise the day before each treatment.Static stretching of hamstring on whole body vibration will include Pre- and post-test active and passive ROM for the both legs, with subjects first undergoing a 5-minute warm-up on a stationary bicycle.
The traditional static stretch consisted of a supine active knee extension on whole body vibration (WBV) at 30 Hz at the "high" amplitude setting will be performed.
The stretch will be held at the point of the onset of discomfort 3 times each for 30 seconds, with a 20-second rest period between each stretch.
Participants will stretch for 4 days per week for 4 weeks.
Active hamstring ROM will be measured via active knee extension using a goniometer with the leg in 90° of hip flexion, with the opposite leg extended.
Passive ROM will be measured via clinician-assist ted knee extension with the leg in 90° of hip flexion.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
change in hamstring range of motion
Time Frame: measurements will be recoded at baseline and end of 4th week
|
pre and post-change in hamstring range of motion will be assessed using a universal goniometer
|
measurements will be recoded at baseline and end of 4th week
|
|
maintenance of change in hamstring range of motion
Time Frame: measurements will be recorded after 15 days of protocol termination
|
hamstring range of motion will be reassessed after 15 days using a universal goniometer
|
measurements will be recorded after 15 days of protocol termination
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Seyyada T Ali, Bahria University Medical and Dental College
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Thompson PD, Arena R, Riebe D, Pescatello LS; American College of Sports Medicine. ACSM's new preparticipation health screening recommendations from ACSM's guidelines for exercise testing and prescription, ninth edition. Curr Sports Med Rep. 2013 Jul-Aug;12(4):215-7. doi: 10.1249/JSR.0b013e31829a68cf. No abstract available.
- Haff, G. (2006). Roundtable Discussion: Flexibility Training. Strength and Conditioning Journal, 28(2).
- Kay AD, Blazevich AJ. Effect of acute static stretch on maximal muscle performance: a systematic review. Med Sci Sports Exerc. 2012 Jan;44(1):154-64. doi: 10.1249/MSS.0b013e318225cb27.
- Wan X, Li S, Best TM, Liu H, Li H, Yu B. Effects of flexibility and strength training on peak hamstring musculotendinous strains during sprinting. J Sport Health Sci. 2021 Mar;10(2):222-229. doi: 10.1016/j.jshs.2020.08.001. Epub 2020 Aug 11.
- Bourne AE. Stretching with whole body vibration versus traditional static stretches to increase acute hamstring range of motion.
- Kokkonen J, Nelson AG, Tarawhiti T, Buckingham P, Winchester JB. Early-phase resistance training strength gains in novice lifters are enhanced by doing static stretching. J Strength Cond Res. 2010 Feb;24(2):502-6. doi: 10.1519/JSC.0b013e3181c06ca0.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 20, 2022
Primary Completion (Actual)
February 20, 2022
Study Completion (Actual)
March 30, 2022
Study Registration Dates
First Submitted
November 4, 2021
First Submitted That Met QC Criteria
December 9, 2021
First Posted (Actual)
December 10, 2021
Study Record Updates
Last Update Posted (Actual)
October 13, 2022
Last Update Submitted That Met QC Criteria
October 11, 2022
Last Verified
October 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- FRC-BUMDC 21/ 2021
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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