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

Hamstring Injury Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05727501
• Other study ID #: zohaibahmad0442
• Status: Completed
• Phase: N/A
• Start date: January 26, 2023
• Est. completion date: July 25, 2023

Study information

• Verified date: August 2023
• Source: Sehat Medical Complex
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

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

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: July 25, 2023
• Est. primary completion date: May 30, 2023
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years to 35 Years

Eligibility

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

Related Conditions & MeSH terms

• Hamstring Injury

Intervention

Other:
• Post isometric relaxation
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 facilitation stretching
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.

Locations

Country	Name	City	State
Pakistan	Pakistan sports board Lahore	Lahore	Punjab

Sponsors (1)

Lead Sponsor	Collaborator
Sehat Medical Complex

Country where clinical trial is conducted

Pakistan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Straight leg raise test. ("change" is being assessed)	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
Primary	The sit to reach test ("change" is being assessed)	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
Primary	The Active Knee Extension Test ("change" is being assessed)	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	The Lower Extremity Functional Scale	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