Assessing Spinal Pain With an Artificial Intelligence-assisted Whole Body Electrical Stimulation Device
CompletedNCT07244237
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
The goal of this observational study is to investigate the correlation between self-reported pain and the measurements obtained using an artificial intelligence-assisted whole-body electrical stimulation device (StimaWELL 120MTRS system) in individuals with chronic back pain. The main question it aims to answer is: Is there any correlation between the pain intensity assessed with StimaWELL 120MTRS system, dolorimeter and self-report in adults with chronic back pain? The patients who have back pain for the duration longer than 3 months and have been eximaned by a medical doctor will be assessed with StimaWELL 120MTRS system, dolorimeter, and will be asked to rate their pain intensity in Numerical Pain Rating Scale.
Study details
- Official title
- Validity of an AI-Supported Whole-Body Electrical Stimulation Device for Spinal Pain Assessment: A Comparison With Self-Reported Pain Scores
- Conditions
- Sponsor
- Amasya University
- Start date
- 2025-11-15
- Primary completion
- 2026-01-15
- Sex
- All
- Age range
- from 18 Years to 60 Years
- Results posted
- No results posted in this snapshot
- Countries
- Turkey (Türkiye)
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Experiencing back pain for more than three months * Experiencing recurrent back pain over the last week * Not having used analgesic or muscle relaxant medications in the last week * Aged between 18 and 60 years * Diagnosed with chronic low back pain by a medical doctor * Literate and able to cooperate with study procedures * Willing to participate in the study Exclusion Criteria: * Having neurological, inflammatory, radiculopathy, vertebral fracture, or similar conditions * Experiencing acute-onset pain * Being pregnant or at risk of pregnancy * Having a psychiatric diagnosis and currently taking medication * Having a skin disease or lesion in the area where electrodes will be applied * Currently undergoing physical therapy * Having vestibular, auditory, or cognitive impairments * Possessing an electronic implant * Having a cardiac arrhythmia * Having a coronary or carotid stent * Being diagnosed with epilepsy * Having severe osteoporosis of the spine
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT07244237