Pain monitoring with wearable electroencephalography.

JRCT ID: jRCT1052230045

Registered date:20/06/2023

Basic Information

• Recruitment status: Pending
• Health condition(s) or Problem(s) studied: Painful orthopaedic disease
• Date of first enrollment: 20/06/2023
• Target sample size: 30
• Study type: Interventional

Intervention(s)

Cold stimulation with cold water or pain stimulation with a tourniquet
Cold stimulation pain of immersing hands in cold water at 0,12, and 15 degrees
200 mmHg and 300 mmHg hemodynamic pain using tourniquet

Outcome(s)

Primary Outcome

AI analysis accuracy of EEG changes caused by painful stimuli (AUROC)
EEG is measured with a telemetric electroencephalograph (304AFBZX00012000)

• Secondary Outcome: Visual analog scale and Numerical Rating Scale during stimulation

Key inclusion & exclusion criteria

• Age minimum: >= 20age old
• Age maximum: < 50age old
• Gender: Both

Include 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.

Exclude criteria

Persons suffering from epilepsy, dementia, or other diseases that affect the EEG
Other subjects deemed unsuitable by the Principal Investigator or Principal Investigator.

Related Information

• Primary Sponsor: Kanie Yuya