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Effects of Facilitated Positional Release Technique ( FPRT) Vs Manual Myofascial Release Technique in Female Patients With Piriformis Syndrome.

Not Applicable
Recruiting
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
Inclusion Criteria
  • • 25-50 years Only females Diagnosed piriformis syndrome Pain from 2 months
Exclusion Criteria
  • Lumbar Radiculopathy Fracture trauma to lumbar spine surgery/ total hip replacement hip OA

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Lower Extremity Functional ScaleBefore 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 PainBefore 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 MotionBefore 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
NameTimeMethod

Trial Locations

Locations (1)

Foundation University College of Physical Therapy

🇵🇰

Islamabad, Pakistan

Foundation University College of Physical Therapy
🇵🇰Islamabad, Pakistan
Ruqia Begum, MS-OMPT
Contact
+92311-5532544
ruqia@fui.edu.pk

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