Actively Recruiting

Phase Not Applicable
Age: 25Years - 50Years
FEMALE
ID06753487

Effects of Facilitated Positional Release Technique versus Manual Myofascial Release Technique in Female Patients with Piriformis Syndrome

Led by Foundation University Islamabad · Updated on 2024-12-31

38

Participants Needed

1

Research Sites

2 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of two different techniques, Facilitated Positional Release Technique (FPRT) and Manual Myofascial Release Technique, in female patients with Piriformis Syndrome. This randomized control trial aims to compare these treatments to see how they impact hip range of motion and pain levels in affected individuals. The study focuses on women aged 25 to 50 who have experienced Piriformis Syndrome symptoms for at least two months. Participants are divided into two groups: a treatment group receiving the Facilitated Positional Release Technique and a control group receiving Manual Myofascial Release. The FPRT involves applying pressure over tender muscle areas while maintaining specific positions, with five repetitions. The control group undergoes 3 to 5 repetitions of manual myofascial release, applying ischemic pressure directly on the piriformis muscle for 90 seconds before release. At the start, baseline measurements of hip range of motion (including abduction, adduction, internal and external rotation), pain levels using the Numeric Pain Rating Scale (NPRS), and functional ability via the Lower Extremity Functional Scale (LEFS) are taken. After two weeks of treatment, these assessments are repeated to compare changes. The primary outcome measured is the change in range of motion after two weeks. The study is sponsored by Foundation University Islamabad and plans to conclude by April 2025.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 25Years - 50Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients diagnosed with Piriformis Syndrome
  • Female patients only
  • Age between 25 and 50 years
  • Pain lasting for at least 2 months
  • Diagnosed with Piriformis Syndrome
Not Eligible

You will not qualify if you...

  • Lumbar radiculopathy
  • Fracture
  • Trauma to the lumbar spine
  • Surgery or total hip replacement
  • Hip osteoarthritis

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - 2 weeks

Participants receive either Facilitated Positional Release Technique or Manual Myofascial Release Technique on the tight Piriformis muscle.

1 baseline visit and 1 follow-up visit

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

F

Fariya Maryam, MS-MSKPT*

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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