Pain monitoring with wearable electroencephalography.
Not Applicable
- Conditions
- Painful orthopaedic disease
- Registration Number
- JPRN-jRCT1052230045
- Lead Sponsor
- Kanie Yuya
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Persons who have given written consent to participate in the research
The age of consent must be between 20 and 50 years old at the time of consent acquisition.
Exclusion Criteria
Persons suffering from epilepsy, dementia, or other diseases that affect the EEG
Other subjects deemed unsuitable by the Principal Investigator or Principal Investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method AI analysis accuracy of EEG changes caused by painful stimuli (AUROC)<br>EEG is measured with a telemetric electroencephalograph (304AFBZX00012000)
- Secondary Outcome Measures
Name Time Method Visual analog scale and Numerical Rating Scale during stimulation