NCT07724704 McGill Versus Sahrmann's Exercises for Chronic Non-Specific Low Back Pain
| NCT ID | NCT07724704 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Riphah International University |
| Condition | Chronic Non-specific Low Back Pain |
| Study Type | INTERVENTIONAL |
| Enrollment | 40 participants |
| Start Date | 2026-07-16 |
| Primary Completion | 2026-09-16 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 40 participants in total. It began in 2026-07-16 with a primary completion date of 2026-09-16.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The goal of this clinical trial is to compare the effects of McGill stabilization exercises and Sahrmann's movement-based exercise protocol in adults with chronic non-specific low back pain. The study aims to determine which exercise program is more effective in reducing pain, improving lumbar range of motion, and decreasing functional disability. The main questions it aims to answer are: Do McGill stabilization exercises reduce pain, improve lumbar range of motion, and decrease disability in individuals with chronic non-specific low back pain? Are McGill stabilization exercises more effective than Sahrmann's movement-based exercise protocol in improving pain, lumbar range of motion, and functional disability? Researchers will compare the McGill stabilization exercise group with the Sahrmann exercise group to determine which intervention provides greater improvements in clinical outcomes. Participants will: Be randomly assigned to either the McGill stabilization exercise group or the Sahrmann exercise group. Receive baseline physiotherapy, including hot pack application, Transcutaneous Electrical Nerve Stimulation (TENS), lumbar isometric exercises, pelvic tilts, knee-to-chest exercises, and manual therapy. Attend supervised treatment sessions 2-3 times per week for 6 weeks. Complete outcome assessments before and after treatment using the Numeric Pain Rating Scale (NPRS) for pain, the Oswestry Disability Index (ODI) for disability, and a bubble inclinometer to measure lumbar range of motion. This study will provide evidence on the comparative effectiveness of two commonly used physiotherapy exercise protocols and help identify the most effective rehabilitation approach for managing chronic non-specific low back pain.
Eligibility Criteria
Inclusion Criteria * Adults aged 20-50 years. * Male and female participants. * Diagnosed with chronic non-specific low back pain lasting more than 12 weeks. * Pain intensity of 3-4 on the Numeric Pain Rating Scale (NPRS) at baseline. * Able and willing to participate in the exercise program and attend all treatment sessions. * Willing to provide written informed consent. Exclusion Criteria * History of spinal surgery. * Presence of neurological deficits. * Structural spinal deformities. * Pregnancy or within 6 months postpartum. * Presence of red flag signs or systemic illness (e.g., fracture, infection, malignancy, inflammatory disorders). * Individuals unable or unwilling to participate in the exercise program or complete the study protocol.
Contact & Investigator
Annum Manzoor, MS OMPT
PRINCIPAL INVESTIGATOR
Gulab Devi Teaching institute
Frequently Asked Questions
Who can join the NCT07724704 clinical trial?
This trial is open to participants of all sexes, aged 20 Years or older, up to 50 Years, studying Chronic Non-specific Low Back Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07724704 currently recruiting?
Yes, NCT07724704 is actively recruiting participants. Contact the research team at imran.amjad@riphah.edu.pk for enrollment information.
Where is the NCT07724704 trial being conducted?
This trial is being conducted at Lahore, Pakistan.
Who is sponsoring the NCT07724704 clinical trial?
NCT07724704 is sponsored by Riphah International University. The principal investigator is Annum Manzoor, MS OMPT at Gulab Devi Teaching institute. The trial plans to enroll 40 participants.