- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06397183
Mulligan Stretch With Traction Versus Post Isometric Relaxtion on Hamstring Flexibility
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
Status
Conditions
Intervention / Treatment
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab
-
Lahore, Punjab, Pakistan, 54000
- Shapes Executive Gym Lahore
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
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
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
Sponsor
Investigators
- Principal Investigator: Muhammad Hassan, MSPT, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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