Assessing Spinal Pain With an Artificial Intelligence-assisted Whole Body Electrical Stimulation Device
Validity of an AI-Supported Whole-Body Electrical Stimulation Device for Spinal Pain Assessment: A Comparison With Self-Reported Pain Scores
Amasya University
200 participants
Nov 15, 2025
OBSERVATIONAL
Conditions
Summary
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.
Eligibility
Inclusion Criteria7
- 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 Criteria12
- 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
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Locations(1)
View Full Details on ClinicalTrials.gov
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NCT07244237