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

N/ACompletedNCT04820699

Riphah International University28 enrolled

Overview

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

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

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

SINGLE

Enrollment

Conditions

Hamstring Injury Hamstring Tendon Injury

Interventions

post isometric relaxation and muligan bent leg raiseOTHER

6 week intervention

muligan bent leg raiseOTHER

muligan bent leg raise

Eligibility

Sex: ALLMin age: 13 YearsMax age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

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

Locations (1)

Riphah IU

Lahore, Punjab Province, Pakistan

Outcomes

Primary Outcomes

NUMERIC PAIN RATING SCALE for pain

0-10 Rating,0 means no pain and 10 severe pain

Time frame: 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.

Time frame: 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.

Time frame: 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

Time frame: 2 months

Data from ClinicalTrials.gov

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