Effects of Facilitated Positional Release Technique ( FPRT) Vs Manual Myofascial Release Technique in Female Patients With Piriformis Syndrome.
- Conditions
- Piriformis Syndrome
- Registration Number
- NCT07044869
- Lead Sponsor
- Foundation University Islamabad
- Brief Summary
This study is a randomized control trial, and the purpose of this study is to determine the "Effects of Facilitated Positional Release Technique ( FPRT) Vs Manual Myofascial Release Technique in Female Patients with Piriformis Syndrome.
- Detailed Description
The purpose of this study is to determine the "Effects of Facilitated positional release technique vs manual myofascial release technique in female patietns with piriformis syndrome.
we make 2 groups control and treatment group . we give FPRT technique to treatment group and manual release technique to control group in patients with piriformis syndrome.
first we take base line readings of HIP ROMS( abduction, adduction, internal rotation, external rotation),NPRS and LEFS(lower extremity functional scale)..
after 2 weeks of treatment again we take same readings and compare both readings.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- Female
- Target Recruitment
- 38
- • 25-50 years Only females Diagnosed piriformis syndrome Pain from 2 months
- Lumbar Radiculopathy Fracture trauma to lumbar spine surgery/ total hip replacement hip OA
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Lower Extremity Functional Scale Before and after every 2 sessions for a total of 2 weeks Lower extremity functional scale consisting of 20 questions about lower extremity function is used. The highest possible count is 80 points, indicating greatest function. The least possible count is 0 points, indicating poor function.
Piriformis Pain Before and after every 2 sessions for a total of 2 weeks The NPRS which has eleven points ranging from zero (0) to ten (10) is used to quantify the degree of pain before and after. A score of 0 denotes "no pain", while score of 10 denotes: maximally felt pain".
Range of Motion Before and after every 2 sessions for a total of 2 weeks. The ranges of hip abduction, hip adduction, hip internal and external rotations are measured using goniometer.
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (1)
Foundation University College of Physical Therapy
🇵🇰Islamabad, Pakistan
Foundation University College of Physical Therapy🇵🇰Islamabad, PakistanRuqia Begum, MS-OMPTContact+92311-5532544ruqia@fui.edu.pk