The goal of this prospective study is to validate a wearable EEG seizure detection solution compared to video EEG. Subjects that undergo a clinical video EEG are asked to additionally wear a wearable EEG headband for up to 2 periods of 4h during the video EEG.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
102
Subjects wear epihunter during routine video EEG
Boston Children's Hospital
Boston, Massachusetts, United States
UZ Leuven
Leuven, Belgium
Danish Epilepsy Center
Dianalund, Denmark
Institute of Neurology and Neuropsychology
Tbilisi, Georgia
Sensitivity for electrographic seizures of study device compared to video EEG
The sensitivity for electrographic seizures by the study device compared to manually annotated electrographic seizures on non-video EEG is \> 0.90 (median sensitivity per patient)
Time frame: 9 months
Number of false alarms by study device per hour
The number of false alarms by the study device \< 0.1 per hour (median false detection rate per recording)
Time frame: 9 months
Feasibility testing of automated behavioral testing triggered by automated detection
Assess if automated behavioral testing triggered by automated detection can be used to automatically assess awareness during an absence seizure. Successful if subjects DO NOT react to the testing during an unaware seizure, and DO react during an aware seizure.
Time frame: 3 months
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