Clinical Trial

Post Facilitatiion Stretch and Dry Needling on Hamstring Tightness in Chronic Low Back Pain

Recruiting
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Record status
This record was last updated July 20, 2026 (before its estimated July 31, 2026 completion). Its status may not reflect the trial's current state.
Summary
The aim of this research is to compare the effects of post-facilitation stretch and dry needling on hamstring flexibility, pain, lumbar range of motion, pelvic tilt, and functional status in patients with chronic low back pain. This randomized clinical trial will be conducted at Spine Care Physical Therapy and Rehabilitation Centre (SPRC), Peshawar. The sample size will be 36 participants, who will be randomly divided into two groups: 18 participants in the post-facilitation stretch group and 18 participants in the dry needling group. The study duration will be 3 weeks, with interventions applied three times per week. The sampling technique used will be non-probability purposive sampling, followed by random allocation using the sealed opaque envelope method. Participants aged 20-50 years diagnosed with chronic nonspecific low back pain and having hamstring tightness will be included. Outcome measures used in the study will be Active Knee Extension Test (goniometer) for hamstring flexibility, Numeric Pain Rating Scale (NPRS) for pain, goniometer for lumbar flexion and extension, pelvic inclinometer for pelvic tilt, and Modified Oswestry Disability Index (MODI) for functional disability.
Protocol Amendment History 1 change
critical Recruitment opened 2026-07-21
Trial Details
NCT Number NCT07426562
Lead Sponsor Riphah International University
Conditions Low Back Pain
Enrollment 36 participants
Start Date 2026-02-02
Primary Completion 2026-07-31 (estimated)
Study Completion 2026-08-31 (estimated)
Updated on ClinicalTrials.gov 2026-07-20