Comparing dry needling and IASTM for hamstring tightness in pelvic tilt
Comparative Effects of Dry Needling and Instrument Assisted Soft Tissue Mobilization on Hamstring Tightness in Patients With Posterior Pelvic Tilt.
This study is testing whether dry needling or a special massage technique can help people with tight hamstrings and pelvic tilt feel better and move more easily.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 30 (estimated) |
| Ages | 18 Years to 40 Years |
| Sex | All |
| Sponsor | Riphah International University Academic / other |
| Locations | 1 site (Nankana sahib, Punjab) |
| Trial ID | NCT05931120 on ClinicalTrials.gov |
What this trial studies
This study aims to compare the effects of dry needling (DN) and instrument-assisted soft tissue mobilization (IASTM) on pain, range of motion, and lower extremity functional status in patients experiencing hamstring tightness associated with posterior pelvic tilt. Participants will undergo either DN or IASTM treatment over a specified period, with outcomes measured to assess improvements in their condition. The study addresses a gap in existing literature regarding effective interventions for this specific patient population.
Who should consider this trial
Good fit: Ideal candidates include individuals with hamstring tightness and posterior pelvic tilt who meet specific inclusion criteria related to knee extension and pain duration.
Not a fit: Patients with a history of herniated discs, prior surgeries in the hip, knee, or back, or those with active infections may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide effective treatment options for patients suffering from hamstring tightness and improve their functional mobility.
How similar studies have performed: While there have been successful studies on dry needling and IASTM for other conditions, this specific comparison for hamstring tightness in posterior pelvic tilt is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Lack of greater or equal to 20 degrees of supine active knee extension * Passive SLR less or equal to 75 degrees * Atraumatic back or knee pain greater or equal to 2 weeks * Individuals willing to participate in the required treatment sessions and follow-up assessments * Posterior pelvic tilt 8.9 standard deviation of 4.5 degree Exclusion Criteria: * History of herniated lumbar disc/radiculopathy * Prior surgery in the hip, knee, or back * Self-reported pregnancy * History of blood borne pathogens/infectious disease/active infection * Metal allergy * Positive instability tests indicative of ligamentous tear * Positive meniscal tests
Where this trial is running
Nankana sahib, Punjab
- DHQ Nankana sahib — Nankana sahib, Punjab, Pakistan (Recruiting)
Study contacts
- Principal investigator: Saba Rafique, phD — Riphah International University
- Study coordinator: imran amjad, phD
- Email: imran.amjad@riphah.edu.pk
- Phone: 03324390125
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.