Last reviewed · How we verify
NCT06749912
Effects of a Lower Back Wrap Device on Lower Back Pain, Physical Function, and Quality of Life
NA trial testing Low back pain wrap in Lower Back Pain in 153 participants. Completed in 23 May 2025.
23 May 2025
Quick facts
| Lead sponsor | State University of New York at Buffalo |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | crossover |
| Masking | none |
| Primary purpose | supportive care |
| Enrollment | 153 |
| Start date | 2 December 2024 |
| Primary completion | 23 May 2025 |
| Estimated completion | 23 May 2025 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Low back pain wrap
Conditions studied
- Lower Back Pain — all drugs for Lower Back Pain →
- Lower Back Pain Chronic — all drugs for Lower Back Pain Chronic →
- Acute Low Back Pain — all drugs for Acute Low Back Pain →
Sponsor
State University of New York at Buffalo
Who can join
Adults 20 to 65, any sex, with Lower Back Pain or Lower Back Pain Chronic. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The goal of this counterbalanced cross-over study is to determine whether a recovery lumbar wrap effectively reduces lower back pain and improves outcomes related to physical function and quality of life in adults with LBP in adults 20-65 years old. This study will also explore whether improvements in other health metrics that are typically related to, or seen in, lower back pain research (i.e. stiffness, mobility, physical activity, validated clinical scoring methods, etc.) are improved with the use of the product. The main question this study aims to answer is: • Does the lumbar wrap effectively reduce low back pain symptoms and improve outcomes related to physical function and quality of life in adults with lower back pain. Participants experiencing lower back pain will be asked to use the lower back wrap for at least 20-minutes per day for a 2-week period, counterbalanced with a 2-week period of no device use. Participants will fill out small daily surveys about their symptoms and complete a pre-, middle-, and post- survey and functional screening to determine efficacy of the device.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT06749912
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other State University of New York at Buffalo trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06749912 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by State University of New York at Buffalo
- Last refreshed: 13 August 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06749912.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing