Non-surgical treatment for chronic low back pain
Research on Effectiveness of Non-surgical Spinal Decompression Therapy and Outcomes With Radiographic Evaluation
This study is testing a non-surgical treatment for chronic low back pain to see if it can help people feel better without needing surgery or strong pain medications.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 42 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | University of South Florida Academic / other |
| Locations | 2 sites (Stanford, California and 1 other locations) |
| Trial ID | NCT06525896 on ClinicalTrials.gov |
What this trial studies
This project aims to evaluate the effectiveness of non-surgical spinal decompression therapy for patients suffering from chronic low back pain (LBP) caused by intervertebral disc issues. The study will involve a double-blinded, randomized design where participants will receive either the active treatment or a placebo over a 12-week period. Comprehensive assessments, including biomechanical evaluations and MRI scans, will be conducted to objectively measure outcomes. The goal is to provide a safer alternative to invasive procedures and reduce reliance on opioids for pain management.
Who should consider this trial
Good fit: Ideal candidates are individuals diagnosed with chronic low back pain for at least three months due to intervertebral disc pathology or related conditions.
Not a fit: Patients with serious spinal pathologies, other chronic pain conditions, or those unable to comply with treatment schedules may not benefit from this study.
Why it matters
Potential benefit: If successful, this treatment could offer a non-invasive solution for chronic low back pain, improving patients' quality of life and reducing dependence on opioids.
How similar studies have performed: Other studies have shown promise with non-surgical spinal decompression therapies, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: \- Diagnosis of chronic LBP for a minimum of 3 months caused by pathological intervertebral disc, degenerative disc disease, posterior facet syndrome, and/or sciatica. Exclusion Criteria: * Known serious spinal pathology (e.g., vertebral fracture, tumor, osteoporosis) * Evidence of central nervous system involvement of pain * Other chronic pain conditions * Pregnancy * Spinal fusion * Inability to comply with treatment schedule * Inability to complete MRIs (e.g., claustrophobia, pacemaker, ferromagnetic implants)
Where this trial is running
Stanford, California and 1 other locations
- Stanford University — Stanford, California, United States (Active_not_recruiting)
- University of South Florida — Tampa, Florida, United States (Recruiting)
Study contacts
- Principal investigator: Nathan D Schilaty, DC, PhD — University of South Florida
- Study coordinator: Nathan D Schilaty, DC, PhD
- Email: MCOM-SchilatyNeubacLab@usf.edu
- Phone: (813) 974-1377
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.