Clinical Trial

Foam Rolling and Dynamic Stretching in Piriformis Syndrome

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Record status
This record was last updated December 11, 2025 (before its estimated December 25, 2025 completion). Its status may not reflect the trial's current state.
Summary
To compare the combined effects of foam rolling and dynamic stretching in patients with piriformis syndrome. 1. Warm-Up (2-3 minutes) Objective: Increase blood flow and prepare muscles for stretching. * Marching in Place - 30 seconds * Pelvic Tilts - 10 reps * Gentle Hip Circles - 10 reps each direction 2. Intervention Phase (8-10 minutes) Group 1: Foam Rolling Alone (FR) (\~10 minutes) * Piriformis Foam Rolling: 30-60 sec per side (2-3 sets) * Glutes \& Lower Back Foam Rolling: 30 sec each (2-3 sets) * Hamstrings \& IT Band Foam Rolling: 30 sec each (2-3 sets) Focus: Slow, controlled rolling with sustained pressure on tender spots. Group 2: Foam Rolling + Dynamic Stretching (FR+DS) (\~10-12 minutes) Step 1: Foam Rolling (\~5-6 minutes, same as Group 1) Step 2: Dynamic Stretching (\~5-6 minutes) * Dynamic Piriformis Stretch: Standing knee-to-opposite-shoulder pull (10 reps per leg) * Leg Swings: Forward and sideways (10 reps each leg) * Walking Lunges with Rotation: 10 reps per leg * Hip Circles \& Controlled Butt Kicks: 10 reps each 3. Cool-Down (2-3 minutes) Objective: Reduce muscle tension and promote recovery. * Seated Piriformis Stretch: 30 sec hold per side (2 sets) * Hamstring Stretch: 30 sec hold per leg * Lower Back Stretch (Child's Pose): 30 sec Progression \& Adjustments * Gradual increase in duration or intensity as tolerated. * Modify exercises if discomfort or pain occurs. * After week 4, increase dynamic stretch duration if flexibility improves. Outcome Measures The effectiveness of the intervention will be assessed through the following key outcome measures: 1. Pain Level - Evaluating changes in discomfort intensity during daily activities and movement. 2. Range of Motion (ROM) - Measuring improvements in hip flexibility and mobility.
Trial Details
NCT Number NCT07278193
Lead Sponsor University of Lahore
Conditions Piriformis Syndrome
Enrollment 40 participants
Start Date 2025-10-31
Primary Completion 2025-12-25 (estimated)
Study Completion 2026-01-02 (estimated)
Updated on ClinicalTrials.gov 2025-12-11