Proof-of-Concept Study for Home-Based EEG as an Alternative to Hospital-Grade Brainwave Recording Devices.
Not Applicable
- Conditions
- epilepsy
- Registration Number
- JPRN-UMIN000053101
- Lead Sponsor
- Tohoku University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Male
- Target Recruitment
- 6
Inclusion Criteria
Not provided
Exclusion Criteria
(1) Patients who cannot give consent to participate in the study. (2) Patients with severe intellectual disabilities or neurodevelopmental disorders. (3) Patients exhibiting severe psychiatric symptoms due to depression, bipolar disorder, etc. (4) Patients with a history of status epilepticus. (5) Others whom the principal investigator deems inappropriate for the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Evaluation of whether EEG data acquired with the at-home EEG device is of equivalent quality to existing long-term simultaneous EEG-video recordings for distinguishing the EEG of epilepsy patients.
- Secondary Outcome Measures
Name Time Method Evaluation of whether it can be worn and measured by individuals other than clinical laboratory technicians.