Actively Recruiting

Phase Not Applicable
Age: 20Years - 50Years
All Genders
NCT06534788

Effects of Reciprocal Inhibition Versus Post Facilitation Muscle Energy Technique Along With Conventional Physical Therapy in Patients With Piriformis Syndrome: a Randomized Controlled Trial

Led by Foundation University Islamabad · Updated on 2024-08-02

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Participants Needed

1

Research Sites

34 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study is a randomized controlled trial and the purpose of this study is to compare the effects of reciprocal inhibition versus post facilitation muscle energy technique along with conventional physical therapy in patients with piriformis syndrome in terms of pain, range of motion at hip joint and functional disability.

CONDITIONS

Official Title

Effects of Reciprocal Inhibition Versus Post Facilitation Muscle Energy Technique Along With Conventional Physical Therapy in Patients With Piriformis Syndrome: a Randomized Controlled Trial

Who Can Participate

Age: 20Years - 50Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 20 to 50 years
  • Both genders
  • Chronic buttock and hip pain with a score of 3 or higher on NPRS lasting more than 3 months
  • Shortened piriformis muscle with internal rotation less than 30 degrees
  • Score of 8 or more on a 12-point clinical scoring system
  • At least two positive screening tests for piriformis syndrome
Not Eligible

You will not qualify if you...

  • Active infection
  • Lower lumbar radiculopathy
  • Sacroiliac joint dysfunction
  • Malignancies
  • History of trauma
  • Hip arthroplasty
  • Rheumatoid arthritis or osteoarthritis
  • Any neurological dysfunction

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Foundation University College of Physical Therapy

Rawalpindi, Punjab Province, Pakistan, 46000

Actively Recruiting

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Research Team

N

Nimrah Haq, MS-MSKPT*

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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