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

37 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 aged 25 to 50 years who have piriformis syndrome. The study aims to compare the impact of these treatments on hip range of motion and related functional measures. This randomized control trial focuses on women experiencing piriformis syndrome with pain lasting at least 2 months. Participants are divided into two groups: the treatment group receives five repetitions of FPRT, which involves applying pressure over a tender muscle area while holding a specific position. The control group undergoes three to five repetitions of Manual Myofascial Release, applying ischemic pressure directly to the piriformis muscle for 90 seconds before release. Both interventions target the piriformis muscle. Before treatment, baseline measurements of hip range of motion including abduction, adduction, internal and external rotation, along with pain levels and lower extremity function, are recorded. After two weeks of treatment, these measures are repeated to assess changes. The main outcome measured is the change in range of motion after two weeks of therapy, helping to determine the comparative effects of the two techniques.

CONDITIONS

Official 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...

  • Female patients aged 25 to 50 years
  • Diagnosed with piriformis syndrome
  • Experiencing pain for at least 2 months
Not Eligible

You will not qualify if you...

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

AI-Screening

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Trial Site Locations

Total: 1 location

1

Foundation University College of Physical Therapy

Rawalpindi, Punjab Province, Pakistan, 46000

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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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