The ECEALT Chronic Low Back Pain Study
Unknown statusNot applicableNCT05040633
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
Brief summary (from the registry)
The primary objective of this double-blind randomized control trial (RCT) is to evaluate the clinical effectiveness of LLLT as adjunctive therapy to standard exercise treatment in patients with non-specific chronic LBP. Specifically, the study will aim to evaluate the effectiveness of adjunct LLLT in the reduction of pain in patients as well as determine its long-term functional outcomes.
Study details
- Official title
- Evaluating the Clinical Effectiveness of Adjunct Low-level Laser Therapy (ECEALT) in the Management of Chronic Low-Back Pain: A Long-Term, Double-Blind, Randomized Control Trial in Physiotherapy Clinics in Ontario, Canada
- Conditions
- Interventions
- Device: BTL 4110 Smart Laser Therapy Equipment (BTL Industries Ltd, United Kingdom (UK))
- Other: Standard Exercise Therapy
- Sponsor
- Health Rehab and Research Clinic
- Start date
- 2022-10-01
- Primary completion
- 2024-04-30
- Sex
- All
- Age range
- from 18 Years to 65 Years
- Healthy volunteers
- true
- Results posted
- No results posted in this snapshot
- Countries
- Canada
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * are 18-65 years with the ability to give informed consent * report with non - specific chronic low back pain, which is defined as pain of \>3 months duration that occurs in the lumbosacral area of the spine, which may or not have the characteristics of limiting the patient's range of movements, and is not attributable to a recognizable, known pathology (e.g., infection, tumor, osteoporosis, lumbar spine fracture, structural deformity, inflammatory disorder, radicular syndrome, or cauda equina syndrome). * are experiencing pain measured using the Quadruple Visual Analogue Scale between 4 and 7 at the time of assessment will be included to keep homogeneity of pain. Exclusion Criteria: * are under 18 years, and those over 65 years of age * have had past fractures of the bone structures of the spine * have had previous surgery of the spine * have a history of previous surgery of the spine or vertebra; spondylosis, spinal stenosis, lumbar disc herniation * use pacemakers (cardiac or brain) * are pregnant, or those who plan to become pregnant during the course of the study * have acute and/or chronic cardiovascular diseases * have dermatological conditions in the area of irradiation and/or inflammatory skin lesions * have tattoo/tattoos around the area of irradiation * have any sensory deficits as defined by the World Health Organization's working definition * are sensitive/allergic to phototherapy * have neurological disorders as defined by the World Health Organization's working definition * are taking anti-inflammatories or analgesic or psychotropic medications * have any current infections * have a history of drug abuse, either recreational, over the counter or prescription over the last 3 months
Canadian sites (1)
| Facility | City | Province |
|---|---|---|
| Health and Rehab Research Inc. | Mississauga | Ontario |
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT05040633