- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06197945
Effects of Mulligan Bent Leg Raise With and Without Bowen Therapy on Hamstring Tightness in Asymptomatic Adults
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
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Ali Raza, Masters
- Phone Number: 03326099065
- Email: araza.frahs@riphah.edu.pk
Study Locations
-
-
Punjab
-
Lahore, Punjab, Pakistan
- Recruiting
- Physiogic Physiotherapy Clinic
-
Contact:
- Dr. M Hashim
- Phone Number: 03234071564
- Email: info@physiogic.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
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
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
Sponsor
Investigators
- Principal Investigator: Ali Raza, Masters, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR&AHS/23/0152
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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