Mulligan Stretch With Traction Versus Post Isometric Relaxtion on Hamstring Flexibility

November 12, 2024 updated by: Riphah International University

Comparison Of Mulligan Stretch With Traction Technique And Post Isometric Relaxation On Hamstring Flexibility In Athletes

The design of my study will be Randomized Control Trial (RCT) study. And the sampling technique will be non-probability convenience sampling. A sample of 32 (16 in each group) has been selected using 10% level of significance and 80% power of test.

Three groups will be made each containing 16 participants with inclusion criteria met. Group A will be given control group treatment with Muscle Energy Technique applied over the period of 4 weeks. Group B will be given control group treatment with Mulligan Stretch with Traction Technique applied over the period of 4 weeks.

Total 3 recordings of Hip Flexion ROMs shall be taken with manual goniometry as follows initial/first day, 3rd week, final week/last treatment. A sum of 8 treatments shall be given to the intervention group over the period of 4 weeks, 2 treatments per week.

Study Overview

Detailed Description

INTRODUCTION:

Mobility in human gait depends on flexibility of hamstring muscles. Hamstring muscles function is hip extension and knee flexion. In most of the population, tightness or shortening of hamstring muscles occur which limits hip flexion. To measure hamstring muscles flexibility simple passive SLR is performed and range is recorded by manual goniometer. To increase SLR, several techniques are used: MET's and TSLR. Effectiveness of these techniques depend on muscle flexibility.

OBJECTIVE:

The purpose of this study is to compare the effectiveness of mulligan stretch with traction technique and muscle energy technique to increase the SLR in athletes with hamstring tightness.

METHOD:

The data will be collected from Athletes in sports clubs, gyms, and sports fields of Lahore. The study will be completed in a period of six months after the approval of synopsis. The design of my study will be Randomized Control Trial (RCT) study. And the sampling technique will be non-probability convenience sampling. A sample of 32 (16 in each group) has been selected using 10% level of significance and 80% power of test.

Three groups will be made each containing 16 participants with inclusion criteria met. Group A will be given control group treatment with Muscle Energy Technique applied over the period of 4 weeks. Group B will be given control group treatment with Mulligan Stretch with Traction Technique applied over the period of 4 weeks.

Total 3 recordings of Hip Flexion ROMs shall be taken with manual goniometry as follows initial/first day, 3rd week, final week/last treatment. A sum of 8 treatments shall be given to the intervention group over the period of 4 weeks, 2 treatments per week.

Study Type

Interventional

Enrollment (Actual)

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 Locations

    • Punjab
      • Lahore, Punjab, Pakistan, 54000
        • Shapes Executive Gym 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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Both male and female
  • Negative Spring test
  • Asymptomatic
  • SLR < 80⸰

Exclusion Criteria:

  • Positive LBP
  • Lumbar Straightening
  • SI Joint Dysfunction
  • History of hamstring injury
  • Current musculoskeletal pain in hip region
  • Any other comorbidity limiting joint ROM

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
Experimental: Mulligan Strech with Traction Group
The Mulligan traction straight leg raise (TSLR) technique is a mobilization technique that can increase hamstring flexibility and range of motion.
Experimental: Post-Isometric Relaxation Group
Post-Isometric Relaxation Technique is a Muscle Energy Technique which increases hamstring flexibility and range of motion.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hip Flexion Range of Motion
Time Frame: Baseline, 3rd week and 6th week.
Hip Flexion ROM will be measured using SLR technique with manual goniometry.
Baseline, 3rd week and 6th week.

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Muhammad Hassan, MSPT, 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)

April 25, 2024

Primary Completion (Actual)

July 25, 2024

Study Completion (Actual)

August 1, 2024

Study Registration Dates

First Submitted

April 29, 2024

First Submitted That Met QC Criteria

April 29, 2024

First Posted (Actual)

May 2, 2024

Study Record Updates

Last Update Posted (Estimated)

November 14, 2024

Last Update Submitted That Met QC Criteria

November 12, 2024

Last Verified

November 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • REC/RCR&AHS/21/0419

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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