Post Isometric Relaxation and Mulligan Bent Leg Raise on Hamstring Tightness in High School Students

Comparative Study of Post Isometric Relaxation and Mulligan Bent Leg Raise on Hamstring Tightness in High School Students

This project was a Randomized clinical trial conducted COMPARATIVE STUDY OF POST ISOMETRIC RELAXATION AND MULLIGAN BENT LEG RAISE ON HAMSTRING TIGHTNESS IN HIGH SCHOOL STUDENTS

Study Overview

• Status: Completed
• Conditions: Hamstring Injury; Hamstring Tendon Injury
• Intervention / Treatment: Other: post isometric relaxation and muligan bent leg raise; Other: muligan bent leg raise

Detailed Description

Non Probability Convenient sampling was done. Patients following eligibility criteria from high schools located in vicinity of Jhang district were considered. Sample size was calculated with Epitool calculator. 28 Participants were randomly allocated in two groups equally via convenient sampling method. Baseline assessment was done initially. Group A was given post isometric relaxation and Group B was given mulligan bent leg raise Duration of research was almost 6 months. All 28 involved subjects were given 12 treatment sessions over a six-week period, which consisted of 02 treatment sessions per week . Then tightness of hamstrings was assessed by AKET, SLR and FTF test. The baseline outcome measures consisted of pain assessment using Numeric rating scale (NPRS), knee joint goniometry in active knee extension test (AKET) and straight leg raise (SLR), modified finger to floor test (FTF) to assess the flexibility of hamstring muscles. . All participants were provided written informed consent prior to commencement of the procedures. Data was analyzed by using SPSS version 23.

• Study Type: Interventional
• Enrollment (Actual): 28
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Pakistan
  • Punjab
    • Lahore, Punjab, Pakistan, 54000
      • Riphah IU

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 13 years to 18 years (ADULT, CHILD)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

Inclusion Criteria:

Asymptomatic Individuals of both gender, aged 13 to 18 years were evaluated for unilateral or bilateral Hamstring tightness. Those who were unable to reach more than 160 degree of knee extension with hip held at 90 degree of flexion, as measured with the thigh held at 90 degrees of hip flexion), unable to complete SLR and meet the criteria of finger to floor test

were included.

Exclusion Criteria:

Individuals were excluded who presented with previous injury of lower limb or pain duration of one year. Also any deformities related to spine, hip and knees or any neurological disorder or with history of lower limb fracture or surgery were also excluded.Subjects with hamstring tightness associated with muscle soreness or with Inflammatory condition that could affect motion were also exluded from the study

Study Plan

How is the study designed?

Design Details

• Primary Purpose: TREATMENT
• Allocation: RANDOMIZED
• Interventional Model: PARALLEL
• Masking: SINGLE

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
EXPERIMENTAL: post isometric relaxation; Group A received Post isometric relaxation technique (MET).The participants performed isometric contractions using 20% of their strength, 5 second holds with 5 seconds rest time in between each contraction	Other: post isometric relaxation and muligan bent leg raise; 6 week intervention
EXPERIMENTAL: mulligan bent leg raise; Group B: Mulligan bent leg raise technique. Isometric contraction of hamstring muscle for progressively five greater position of hip flexion; three pain-free repetitions with 5 second hold was performed by participants	Other: muligan bent leg raise; muligan bent leg raise

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
NUMERIC PAIN RATING SCALE for pain	0-10 Rating,0 means no pain and 10 severe pain	2 months
Knee joint goniometry in active knee extension test (AKET)	The 90/90 test, also known as the Active Knee Extension (AKE) Hamstring Flexibility Test, measures hamstring flexibility, particularly when the hip is flexed. purpose: to assess the range of active knee extension in a position of hip flexion, as required in running and kicking.	2 months
straight leg raise (SLR) test	If symptoms are primarily back pain, it is most likely the result of a disc herniation applying pressure on the anterior theca of the spinal cord, or the pathology causing the pressure is more central. "Back pain only" patients who have a disc prolapse have smaller, more central prolapses.[1] If pain is primarily in the leg, it is more likely that the pathology causing the pressure on neurological tissue(s) is more lateral.[1] Disc herniations or pathology causing pressure between the two extremes are more likely to cause pain in both areas.	2 months
modified finger to floor test (FTF)	If the FTF test is limited by pain, the location and pain score out of 10 should be should be documented. If the FTF test is 0cm or the patient is able to place their palms to the floor with no pain, 10 with maximum pain	2 months

Collaborators and Investigators

• Sponsor: Riphah International University
• Investigators: Principal Investigator: warda saleem, MS, Riphah International University

Publications and helpful links

General Publications

• Kalanekar TA, Koley S. A Comparative Study of Mulligans Bent Leg Raise versus Muscle Energy Technique in Asymptomatic Individuals with Hamstring Tightness.

Study record dates

Study Major Dates

• Study Start (ACTUAL): January 15, 2019
• Primary Completion (ACTUAL): June 15, 2019
• Study Completion (ACTUAL): August 15, 2019

Study Registration Dates

• First Submitted: March 26, 2021
• First Submitted That Met QC Criteria: March 26, 2021
• First Posted (ACTUAL): March 29, 2021

Study Record Updates

• Last Update Posted (ACTUAL): May 11, 2021
• Last Update Submitted That Met QC Criteria: May 7, 2021
• Last Verified: May 1, 2021

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Wounds and Injuries; Tendon Injuries
• Other Study ID Numbers: REC/Lhr/18/1008

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