Effects of sensorimotor training with and without myofascial release for sciatica
Official title: Effects of Somatosensory Motor Control With and Without Myofascial Release on Pain, Lumbar Range of Motion and Functional Disability in Patients With Sciatica
Run by Riphah International University · NCT06696898 · Data updated 2026-11-12
This study is testing whether adding myofascial release to sensorimotor training can help people with sciatica feel less pain and move better.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 25 Years to 50 Years |
| Sex | All |
| Enrollment | 74 (estimated) |
| Sponsor | Riphah International University Academic / other |
| Locations | 1 site (Lahore, Punjab Province) |
| Status | Recruiting |
| Started | September 1, 2024 |
| Main results expected | February 28, 2025 |
| Study ends | May 30, 2025 |
| Registry record updated | November 20, 2024 |
| Trial ID | NCT06696898 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients diagnosed with unilateral sciatica pain lasting at least three months and experiencing significant disability.
✕Probably not a fit
Patients with recent lumbar spine surgery, severe comorbidities, or contraindications to physical therapy may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study evaluates the effectiveness of sensorimotor control training combined with myofascial release techniques in patients suffering from sciatica. Participants diagnosed with unilateral sciatica pain will be randomly assigned to two groups: one receiving sensorimotor training with routine physical therapy and the other receiving the same training with added myofascial release. The study aims to assess improvements in pain levels, lumbar range of motion, and functional disability. By comparing these two approaches, the research seeks to fill gaps in understanding the best therapeutic strategies for managing sciatica.
Why it matters
Potential benefit: If successful, this study could provide a more effective treatment option for patients suffering from sciatica, potentially reducing pain and improving mobility.
How similar studies have gone: Previous studies have shown promising results for similar approaches, indicating potential effectiveness in managing sciatica.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patient Diagnosed with sciatica (confirmed by clinical examination and imaging) * Patient with Unilateral sciatica pain * Patient Experiencing symptoms for at least 3 months * Pain (VAS) score ≥ 5) in the lumbar and/or lower extremity region in patients. * The disability with a score of at least 20% by the Oswestry Disability Index ( * Stable patient , no recent changes in treatment regimen for sciatica within the past 4 weeks Exclusion Criteria: * Patients with Lumbar spine surgery history within the past 6 months (11) * Patients who have been Another clinical trial participant within the past 3 months (1). * Patients with Physical therapy interventions contraindicated like in Severe cardiovascular disease and Uncontrolled hypertension Acute disc herniation requiring urgent surgical intervention (10). * Patients with Significant comorbidities like malignancy, spinal infection and Severe osteoporosis affecting spine stability (14). * Inability in patients to communicate effectively in Urdu or English, hindering comprehension of study instructions and assessments.
Where it's running
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Well Versed Physio clinic
Lahore, Punjab Province, Pakistan Recruiting
Study contacts
- Principal investigator: Aruba Saeed, Phd — Riphah International University
- Study coordinator: Imran amjad, Phd
- Email: imran.amjad@riphah.edu.pk
- Phone: 03324390125
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.