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

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07044869
Enrollment
38
Registered
2025-07-01
Start date
2024-07-26
Completion date
2025-08-20
Last updated
2025-07-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Piriformis Syndrome

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.

Interventions

Participants in experimental group A receive FPRT as a main intervention along with piriformis stretches. 30 minutes' session starts with application of 10 minutes hot pack, followed by FPRT and stretches respectively. For FPRT, the patient position was prone with the hip flexion approximately (60°-90°) and abduction. The therapist was seated on the side that was affected, and the treated leg was hanging off the table with the knee bent resting on the therapist thigh. The painful tender area was felt in the piriformis muscle's belly around midway between the greater trochanter and the inferior lateral angle of sacrum. At the point when tender area was palpated, therapist applied ischemic pressure over the area with finger pads. Pressure hold for 1 minute and two repetitions were performed (2 minutes' pressure for whole was given). After that piriformis stretches were performed with 5reps\*5 sec hold\*1set.

Experimental Group B participants received MFRT as a main intervention along with application of hot pack and piriformis stretches. They also received 30 min session started with application of hot pack for 10 minutes followed by MFRT and piriformis stretches. For application of MFRT patient was in prone lying position. The therapist was standing at the affected/unaffected side of the patient. Myofascial release was provided, using the therapist's palm, finger pads or elbow directly on the piriformis muscle, pressure was provided on the tender area directly and held for a while (60 seconds approx.) and 3 repetitions were performed. Back and forth little kneading motions were applied in accordance with the muscle fiber's direction. After MFRT piriformis stretches were performed with frequency of 5 repetitions \*5 second hold\* 1 set.

Sponsors

Foundation University Islamabad
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

Randomized Control Trial

Eligibility

Sex/Gender
FEMALE
Age
25 Years to 50 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Piriformis PainBefore and after every 2 sessions for a total of 2 weeksThe 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.
Lower Extremity Functional ScaleBefore and after every 2 sessions for a total of 2 weeksLower 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.
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.

Countries

Pakistan

Contacts

Primary ContactFariya Maryam, DPT
fariyamaryam9@gmail.com+923102541357

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026