"Effects of Passive Static Stretching of 30 Seconds Versus 60 Seconds on the Hamstring Flexibility in Adults With Hamstring Tightness.

May 27, 2024 updated by: Foundation University Islamabad

This study is a randomised controlled trial and the purpose of this study is to determine the effects of Passive Static Stretching of 30 seconds versus 60 seconds on the Hamstring Flexibility in adults with Hamstring Tightness.

The study is conducted in Rehabilitation department of Fauji Foundation Hospital on the sample of 38 participants. Hamstring flexibility will be evaluated at the beginning by Active knee extension test.

The subjects will be randomized into two group by sealed envelope method. Baseline assessment would be done by using tools of SLR and modified knee extension test and then final assessment will be done after 4 weeks.

Study Overview

Detailed Description

The purpose of this study is to determine the effects of passive static stretching on hamstring flexibility in adults with hamstring tightness" adults (age : 18-45 years ) by using

  1. Goniometer
  2. Straight leg raise (SLR)
  3. Passive Hip Flexion Test(PHFT)
  4. Active Knee Extension Test( AKET)
  5. Modified Knee Extension Test(MKET) Data will be collected before and after the intervention protocol for each participant.

Data collection procedure:The subjects will be advised of the training session schedule following the baseline assessment. Pre and post intervention scores will be recorded.

Study Type

Interventional

Enrollment (Estimated)

32

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 Contact

Study Locations

    • Punjab
      • Rawalpindi, Punjab, Pakistan, 4000
        • Recruiting
        • Foundation University College of Physical Therapy
        • Contact:

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

  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion criteria:

  • Adults age ranging from 18-45 years
  • Both males and females are included in the study
  • Individuals with 90 degree hip flexion having a minimum reduction of 15 degrees in knee extension position.

Exclusion criteria :

  • Old adults
  • Individuals suffering from any acute or chronic co-morbidities of musculoskeletal, neurologic, cardiovascular or systemic origin
  • Post-surgical cases
  • Hamstring strain or any other dysfunction in past two years.

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group 1

Week 1 Passive Hip Flexion Test Straight leg Raise Modified Knee Extension Test Passive Static Stretching 3-4 reps 3-5 second hold in each activity Week 2 Passive Hip Flexion Test Straight leg Raise Modified Knee Extension Test Passive Static Stretching 3-4 reps 3-5 second hold in each activity

Week 3 Passive Hip Flexion Test Straight leg Raise Modified Knee Extension Test Passive Static Stretching 3-4 reps 3-5 second hold in each activity

Week 4 Passive Hip Flexion Test Straight leg Raise Modified Knee Extension Test Passive Static Stretching 3-4 reps 3-5 second hold in each activity

Intervention includes Following Tests

  1. Passive Hip Flexion Test(PHFT)
  2. Straight Leg Raises(SLR)
  3. Modified Knee Extension Test(MKET)
Experimental: Group 2

Week 1 Passive Hip Flexion Test Straight leg Raise Modified Knee Extension Test Passive Static Stretching 3-4 reps 3-5 second hold in each activity Week 2 Passive Hip Flexion Test Straight leg Raise Modified Knee Extension Test Passive Static Stretching 3-4 reps 3-5 second hold in each activity Week 3 Passive Hip Flexion Test Straight leg Raise Modified Knee Extension Test Passive Static Stretching 3-4 reps 3-5 second hold in each activity

Week 4 Passive Hip Flexion Test Straight leg Raise Modified Knee Extension Test Passive Static Stretching 3-4 reps 3-5 second hold in each activity

Intervention includes Following Tests

  1. Passive Hip Flexion Test(PHFT)
  2. Straight Leg Raises(SLR)
  3. Modified Knee Extension Test(MKET)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain intensity
Time Frame: 4 weeks
Numeric Pain Rating Scale has a scale of 0-10 or 0-100 points and can be given verbally or in writing.
4 weeks
Range of motion
Time Frame: 4 weeks
Goniometer will be used
4 weeks
Physical Function
Time Frame: 4 weeks
Physical Function will be assessed using Oswestry disability Questionairre
4 weeks
Lumbar range of motion
Time Frame: 4 Weeks
Using Inclinometer
4 Weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this 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)

July 15, 2023

Primary Completion (Actual)

November 20, 2023

Study Completion (Estimated)

June 20, 2024

Study Registration Dates

First Submitted

May 27, 2024

First Submitted That Met QC Criteria

May 27, 2024

First Posted (Actual)

May 31, 2024

Study Record Updates

Last Update Posted (Actual)

May 31, 2024

Last Update Submitted That Met QC Criteria

May 27, 2024

Last Verified

May 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • FUI/CTR/2024/9

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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