Pain, placebo, and test of treatment efficacy: a narrative review.
Lene Vase, Karolina Wartolowska
https://pubmed.ncbi.nlm.nih.gov/30915982/Actively Recruiting
Led by Hopital Foch · Updated on 2026-08-03
76
Participants Needed
1
Research Sites
N/A
Total Duration
Chronic neck pain, a common condition causing disability and reduced mobility, often relies on medication-based treatments. However, non-drug therapies are recommended but underused due to limited evidence and awareness. This trial evaluates the SCENAR device, an electrotherapy tool delivering electrical impulses through the skin, to assess its impact on pain, function, and disability in adults with chronic non-specific neck pain. Participants will receive either five sessions of active SCENAR therapy or sham therapy applied to the painful cervical area. Each session lasts about 20 minutes, with intensity adjusted by patient feedback in the active group, while the sham group receives the device without electrical stimulation. The study compares these two approaches over approximately 10 weeks, including treatment and follow-up. During the trial, participants will be assessed for changes in their Neck Disability Index score, pain intensity at rest and during movement, and overall impression of change. Researchers will also monitor treatment adherence and evaluate psychological and social factors at baseline. Follow-up occurs two weeks after the last treatment session, with total participation lasting around 10 weeks to measure outcomes and safety.
CONDITIONS
SCENAR Therapy in Chronic Non-specific Neck Pain
M
Mireille Michel-Cherqui, MD
M
Marjolaine Ngollo, PhD
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Hopital Foch
Lead Sponsor
Fondation Apicil
Collaborating Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Approximately 8 weeks
Participants receive five sessions of either active SCENAR therapy or sham therapy applied to the painful neck area over several weeks.
Five treatment visits
Duration - 2 weeks
Participants are assessed for changes in neck disability and pain two weeks after completing the last SCENAR session.
1 follow-up visit
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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https://pubmed.ncbi.nlm.nih.gov/11701584/Hopital Foch
Lead Sponsor
Fondation Apicil
Collaborating Sponsor