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Study on the Effect of Personalized Exercise Programs on Pain and Nerve Function in People with Piriformis Syndrome.

The Role of Tailored Exercise Interventions on Clinical and Neural Outcomes in Patients with Piriformis Syndrome: A Randomized Controlled Trial - NO

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/088259
Enrollment
60
Registered
2025-06-04
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Health Condition 1: M00-M99- Diseases of the musculoskeletal system and connective tissue

Interventions

Intervention1: Tailored Exercise Program (TEP) for Piriformis Syndrome: In randomized controlled trials (RCTs) investigating the role of tailored exercise interventions on clinical and neural outcomes

Sponsors

None
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. A participants aged between 20 to 60 with a clinical diagnosis of Piriformis Syndrome (based on symptoms and physical examination). 2. Evidence of sciatic nerve involvement (positive nerve tension signs and imaging confirmation). 3. Patients with moderate-to-severe pain (e.g., 4-10 on the VAS scale) and functional disability (e.g., score more than 20 on the Oswestry Disability Index). 4. Patients who have not undergone previous invasive treatments (e.g., surgery, corticosteroid injections) within the last 3 months.

Exclusion criteria

Exclusion criteria: 1. The patients had a previous surgical history involving the lumbar and/or hip region, abdominal cavity tumors, anatomic variations of the sciatic nerve. 2. A history of buttock or hip infection, active psychiatric diseases, vascular disease, malignancy, or diabetic neuropathy. and examination of the lumbar spine, pelvis, hips, and sacroiliac joint were used to rule out other causes of sciatica. 3. Pregnancy or conditions that contraindicate physical activity 4. Previous surgery on the hip or pelvis in the last 6 months. 5. Patients with cognitive impairments or who are unable to follow exercise instructions.

Design outcomes

Primary

MeasureTime frame
Ultrasound (US): For muscle thickness (piriformis muscle) Pain: Measuring throughvisual analog scale (VAS) Hip range of motion (ROM): Measuring through Goniometer Muscle Strength: through Manual muscle testing (MMT)Timepoint: At baseline and after 18 session

Secondary

MeasureTime frame
Disability: Measure by Disability Oswestry Disability Index (ODI) Neural Tension: Measuring through Lower Limb Tention Test (LLTT)Timepoint: At baseline and after 18 session

Countries

India

Contacts

Public ContactDr Sajjan Pal

SGT University

Sajjanpal_fpt@sgtuniversity.org9468324923

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026