NCT05069363 Whole-Body Photobiomodulation and Chronic Pain Trial

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 20 participants in total. It began in 2022-01-12 with a primary completion date of 2022-09.

Brief Summary

Chronic pain is a common long-term condition that can affect any area throughout the body. Individuals suffering with chronic pain often have associated fatigue, sleep and mood disturbances. Current treatments for chronic pain include a variety of both medicine-based approaches and non-medical approaches such as exercise and psychology treatments. Patients often take a combination of medications such as antidepressants and strong medications like morphine - which are not always effective, and often associated with several troublesome side effects. Despite physical activity being a common and helpful treatment, evidence shows that patients with chronic pain can find it difficult to engage for a variety of reasons. It would be helpful to see if other non-medication based approaches will be an acceptable treatment to those suffering with chronic pain. Photobiomodulation (PBM) therapy describes a safe, non-invasive low-energy light therapy that has been successful in treating a variety of chronic pain conditions. Cells absorb light to produce a series of reactions that culminate in pain relief, reduced inflammation, and tissue repair. Most studies examining effects of PBM have consisted of a small hand-held probe focused on specific painful areas. There are a cohort of chronic pain conditions that encompass widespread throughout the back, neck and joints, such as fibromyalgia (FM). Whole-body PBM therapy is able to treat a large area of the body in a short space of time. The main purpose of the study is to determine feasibility, with a view to guiding a definitive Randomised Controlled Trial (RCT), in terms of: feasibility of eligibility criteria, recruitment rates, acceptability of trial device in the chronic pain population, and acceptability of outcome measures.

Eligibility Criteria

Inclusion Criteria: Patients eligible for the trial must comply with all of the following: 1. Currently diagnosed or receiving treatment for a widespread chronic pain condition, including but not limited to: 1. Axial pain of any origin 2. Polyathralgia of any origin 3. Myofascial pain of any origin 4. A diagnosis of chronic widespread pain or FM 2. Able to provide informed written consent 3. ≥18 years 4. Able to commit time to the trial treatment schedule of 6 weeks 5. Score as low or moderate risk on the COVID-19 risk stratification tool - applicable for the duration of the pandemic Exclusion Criteria: 1. Pregnancy 2. Severe skin diseases (e.g. skin cancer, severe eczema, dermatitis, or psoriasis) 3. Body weight ≥136kg, as per manufacturer instructions \[see Appendix 3\] 4. Uncontrolled co-morbidities (e.g. uncontrolled diabetes defined as HbA1c \>69mmol/mol, decompensated heart failure, major psychiatric disturbance such as acute psychosis or suicidal ideation) 5. Use of systemic corticosteroid therapy including oral prednisolone or corticosteroid injections within the preceding 6 months as recommended by the manufacturer; steroids are thought to inhibit the anti-inflammatory effect of photobiomodulation therapy 6. Known active malignancy 7. Inability to enter the NovoTHOR device or lie flat for 20 minutes (either due to physical reasons or other e.g. claustrophobia) 8. Patients speaking a language for which an interpreter cannot be sought

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