NCT07026058 Sound Sine Wave And Standard Physiotherapy In Mechanical Low Back Pain
| NCT ID | NCT07026058 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Riphah International University |
| Condition | Low Back Pain |
| Study Type | INTERVENTIONAL |
| Enrollment | 40 participants |
| Start Date | 2025-05-01 |
| Primary Completion | 2025-08-30 |
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 2025-05-01 with a primary completion date of 2025-08-30.
⚠ 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 study design will be a randomized clinical trial (RCT). Sampling technique will be nonprobability convenience sampling. Data will be collected from KKT orthopedic spine center Lahore. Participants will be divided into 2 groups. Group A will receive Sound wave treatment protocol and standard physiotherapy treatment protocol , Group B will receive only Standard Physiotherapy treatment .Both groups will receive TENS and hot pack for 10 minutes. The inclusion and exclusion criteria will be Both gender , aged 18-45 years , Minimum 03 months chronicity of lower back pain , Clinically diagnosed with the help of tests SLR test to rule out nerve root compression or disc herniation, FABER test to rule out SI joint dysfunction ,Scobber Test to assess lumbar flexibility and mobility, Lumber quadrant test to identify pain from facet joints, Lumber extension test and Pain localized to the lumbar region, potentially radiating to the buttocks or thighs but not below the knee. The Exclusion Criteria will be Chronic systemic soft tissue and bony diseases , History of spinal trauma or fractures , Severe spinal stenosis or spondylolisthesis and Pain radiating to one or both legs, consistent with lumbar radiculopathy. The outcome measure tools will be NPRS, inclinometer, x-rays and Oswestry Disability Index (ODI) . Data will be analyzed using SPSS . Ethical Committee of Riphah International University, and informed consent will be secured from all participants.
Eligibility Criteria
Inclusion Criteria: * Both gender Aged 18-45 years * Minimum 03 months chronicity of lower back pain * Clinically diagnosed with the help of tests * SLR test to rule out nerve root compression or disc herniation * FABER test to rule out SI joint dysfunction * Scobber Test to assess lumbar flexibility and mobility * Lumber quadrant test to identify pain from facet joints * Lumber extension test * Pain localized to the lumbar region, potentially radiating to the buttocks or thighs but not below the knee Exclusion Criteria: * Chronic systemic soft tissue and bony diseases * History of spinal trauma or fractures * Severe spinal stenosis or spondylolisthesis * Pain radiating to one or both legs, consistent with lumbar radiculopathy * Participants with a known history of cervical myelopathy, characterized by symptoms of spinal cord compression in the cervical spine (e.g., neck pain with neurological deficits such as weakness, numbness, or abnormal reflexes)
Contact & Investigator
Syed Shakil ur Rehman, PhD
PRINCIPAL INVESTIGATOR
Riphah International University
Frequently Asked Questions
Who can join the NCT07026058 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 45 Years, studying 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 NCT07026058 currently recruiting?
Yes, NCT07026058 is actively recruiting participants. Contact the research team at shakil.urrehman@riphah.edu.pk for enrollment information.
Where is the NCT07026058 trial being conducted?
This trial is being conducted at Lahore, Pakistan.
Who is sponsoring the NCT07026058 clinical trial?
NCT07026058 is sponsored by Riphah International University. The principal investigator is Syed Shakil ur Rehman, PhD at Riphah International University. The trial plans to enroll 40 participants.