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

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
      • 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.

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.

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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