Comparison of Post Isometric Relaxation and Post Facilitation Stretching on Hamstring Muscle Flexibility

August 11, 2023 updated by: Waseem Javaid, Sehat Medical Complex

Comparison of Post Isometric Relaxation and Post Facilitation Stretching on Hamstring Muscle Flexibility in Collegiate Athletes

The goal of this randomized clinical trial is to check the effectiveness of post isometric relaxation and post facilitation stretching on hamstring muscle flexibility in collegiate athletes.

The main question it aims to answer is:

  • To compare the post isometric relaxation and post facilitation stretching techniques on hamstring muscle flexibility in collegiate athletes Participants were divided in two groups,
  • Group-A was treated with baseline treatment of heating for 15min and rehab protocol post isometric relaxation in which 3-5 repetitions for 7-10 seconds hold in each session for three sessions per week in alternate days for four weeks.
  • Group-B was treated with baseline treatment of heating for 15min and rehab protocol post facilitation in which 3-5 repetitions for 7-10 seconds hold in each session for three sessions per week in alternate days for four weeks.

Study Overview

Detailed Description

Hamstring injuries are most common injuries in sports and there are many treatment methods and rehabilitation protocols available which are used according to the extent of injury. The main purpose of this study was to check the effectiveness of two treatment techniques on the hamstring muscle flexibility in collegiate athletes. Muscle Energy Techniques (MET) and their related post-isometric relaxation and post facilitation stretching techniques have demonstrated better results in improving flexibility of the tightened muscles. The study was a randomized clinical trial at Pakistan sports board and coaching center Lahore in which convenience sampling technique was used. This study included total 48 participants and for this purpose Open Epi tool software was used as a sample size calculation. Participants falling in this category were recruited into the study, those were male athletes with ages 18 to 35 having bilateral hamstring muscle tightness and acute hamstring injuries. Participants failing to fall in this category were excluded of the study such as females and athletes with hip, buttock and low back pain radiating to back of thigh and history of fractures within 6 months. Universal goniometer, SLR, active knee extension test and sit to reach test would be used as a tool for pre and post assessment of athletes. In this study the subjects were assigned through convenience sampling into two groups. Group A was treated with post isometric relaxation technique and group B was treated with post facilitation technique. Data will analyze through SPSS version 25.0

Study Type

Interventional

Enrollment (Actual)

30

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

    • Punjab
      • Lahore, Punjab, Pakistan, 54000
        • Pakistan sports Board Lahore

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 35 years (Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • • Age 18 to 35

    • Male
    • Athletes with hamstring muscle tightness (bilateral) or Acute hamstring injuries

Exclusion Criteria:

  • • Athletes with hip, buttocks and low back pain radiating to back of thigh

    • History of fracture within 6 months

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: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Post isometric relaxation
This Group was treated with baseline treatment of heating for 15min and rehab protocol post isometric relaxation in which 3-5 repetitions for 7-10 seconds hold in each session for three sessions per week in alternate days for four weeks.
post isometric relaxation in which 3-5 repetitions for 7-10 seconds hold in each session for three sessions per week in alternate days for four weeks.
Active Comparator: Post facilitation stretching
This Group was treated with baseline treatment of heating for 15min and rehab protocol post facilitation stretching in which 3-5 repetitions for 7-10 seconds hold in each session for three sessions per week in alternate days for four weeks.
post facilitation stretching in which 3-5 repetitions for 7-10 seconds hold in each session for three sessions per week in alternate days for four weeks.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Straight leg raise test. ("change" is being assessed)
Time Frame: Change from Baseline range of motion at 4 weeks
Straight leg raise (SLR) is a fundamental maneuver during the physical examination of a patient with lower back pain. The straight leg raise test is performed with the patient in a supine position. The examiner gently raises the patient's leg by flexing the hip with the knee in extension, and the test is considered positive when the patient experiences pain along the lower limb in the same distribution of the lower radicular nerve roots (usually L5 or S1)
Change from Baseline range of motion at 4 weeks
The sit to reach test ("change" is being assessed)
Time Frame: Change from Baseline range of motion at 4 weeks
The sit and reach test is a common measure of flexibility, and specifically measures the flexibility of the lower back and hamstring muscles. The starting position for the SR test places the subject's feet against the box relative to the 38.1cm point. After the reach position of the test, the criterion score is 38.1cm plus or minus the distance reached during the test.
Change from Baseline range of motion at 4 weeks
The Active Knee Extension Test ("change" is being assessed)
Time Frame: Change from Baseline range of motion at 4 weeks
The Active Knee Extension Test is used to assess hamstring muscle length and the range of active knee extension in the position of hip flexion. The AKE test subjects were positioned so that the thigh was in contact with the crossbar on the wooden frame apparatus, and the thigh was a t a 90" angle (as measured with the universal goniometer) with the trunk. Subjects were told to extend their knee while maintaining contact with the crossbar.
Change from Baseline range of motion at 4 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Lower Extremity Functional Scale
Time Frame: 4 weeks of intervention
The Lower Extremity Functional Scale is a questionnaire containing 20 questions about a person's ability to perform everyday tasks. It is efficient to administer and score and is applicable for research purposes and clinical decision making for individual patients. Its maximum score is 80. The lower the score the greater the disability.
4 weeks of intervention

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Hafiz Zohaib Ahmed, MS-SPT, Riphah International University

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 26, 2023

Primary Completion (Actual)

May 30, 2023

Study Completion (Actual)

July 25, 2023

Study Registration Dates

First Submitted

January 26, 2023

First Submitted That Met QC Criteria

February 4, 2023

First Posted (Actual)

February 14, 2023

Study Record Updates

Last Update Posted (Actual)

August 15, 2023

Last Update Submitted That Met QC Criteria

August 11, 2023

Last Verified

August 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • zohaibahmad0442

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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