Effects of Mulligan Bent Leg Raise With and Without Bowen Therapy on Hamstring Tightness in Asymptomatic Adults

January 8, 2024 updated by: Riphah International University

Hamstring tightness is a common problem caused by a sedentary lifestyle and can have negative effects on posture and musculoskeletal function. It can lead to postural misalignment, increasing loading on the lumbar spine, increased pressure on inter-vertebral disc and potentially resulting in low back problems. Bowen technique and Mulligan Bent leg raise is used to treat conditions including hamstring tightness.

The goal of this clinical trial is to compare the effects of mulligan bent leg raise with and without Bowen therapy on hamstring tightness in asymptomatic adults.

Study Overview

Detailed Description

A randomized control trial will be conducted at Riphah Rehabilitation Center and Physiogic Physiotherapy clinic on 50 asymptomatic adults who meet the inclusion criteria will be recruited using non probability purposive sampling and randomly allocated using Random Allocation Software 2.0. Informed consent will be obtained from all participants. They will be divided into two groups which will contain 25 participants in each group. Group A will receive three alternate sessions of Mulligan Bent Leg Raise with Bowen therapy and Group B will receive three alternate sessions of Mulligan Bent leg Raise. The Mulligan Bent Leg Raise technique will be performed with 3 repetition, 3-4 times with 20 sec hold and one minute rest between each repetition.

Study Type

Interventional

Enrollment (Estimated)

50

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 Contact

Study Locations

    • Punjab
      • Lahore, Punjab, Pakistan
        • Recruiting
        • Physiogic Physiotherapy Clinic
        • Contact:

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:

  • Male/Female
  • Age group between 18-40 years
  • Unilateral limitation of SLR less than 75 degrees
  • Asymptomatic, active knee extension less than 160 degrees

Exclusion Criteria:

  • Fracture of Lower limb
  • Individuals with soft tissue injury
  • Chronic back pain
  • Prolapsed Intervertebral disc
  • Any surgery was done for back, pelvis hip or knee.
  • Spinal deformity

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 bent leg raise
The Mulligan Bent Leg Raise technique will be performed with 3 repetition, 3-4 times with 20 sec hold and one minute rest between each repetition.
Mulligan bent leg raise
Experimental: Mulligan bent leg raise with Bowen therapy
The Mulligan Bent Leg Raise technique will be performed with 3 repetition, 3-4 times with 20 sec hold and one minute rest between each repetition. After that Bowen therapy will be applied on hamstring bilateral.
Mulligan bent leg raise with Bowen therapy

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Active Knee Extension Test
Time Frame: 1 week
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. A knee flexion angle of 20 ° or less is considered normal ROM on the AKE. The AKE has been found to have high reliability for intra-rater agreement (ICC = .86-.99) and moderate inter-rater reliability (ICC = .76-.89)
1 week
Sit and Reach Test
Time Frame: 1 week
The Sit and reach test is one of the linear flexibility tests which helps to measure the extensibility of the hamstrings and lower back. Previous studies indicated that reliability estimate for Sit and reach test are consistently higher (.96 < R < .99)
1 week
Straight Leg Raise Test
Time Frame: 1 week
also called the Lasegue test, Normal ROM for the PSLR has been reported as 80 ° of hip flexion. The PSLR has been reported to have high intra-rater (r = .91) and inter-rater (r = .93) reliability
1 week

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Ali Raza, Masters, 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)

August 3, 2023

Primary Completion (Estimated)

January 10, 2024

Study Completion (Estimated)

February 10, 2024

Study Registration Dates

First Submitted

December 26, 2023

First Submitted That Met QC Criteria

January 8, 2024

First Posted (Actual)

January 9, 2024

Study Record Updates

Last Update Posted (Actual)

January 9, 2024

Last Update Submitted That Met QC Criteria

January 8, 2024

Last Verified

December 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • REC/RCR&AHS/23/0152

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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