Pain monitoring with wearable electroencephalography.

Pain monitoring using wearable electroencephalography with healthy people.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-jRCT1052230045

Enrollment

Registered

2023-06-20

Start date

2023-06-20

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Painful orthopaedic disease

Interventions

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 tourn

D063189

Eligibility

Sex/Gender

All

Inclusion criteria

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

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.

Design outcomes

Primary

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

Secondary

Measure	Time frame
Visual analog scale and Numerical Rating Scale during stimulation	—

Contacts

Public ContactYuya Kanie

Osaka University Hospital

ykanie@ort.med.osaka-u.ac.jp+81-6-6879-3552

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026