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Testing an ear-worn device to detect seizures in people with epilepsy

Tests an ear-worn device that detects seizures, compared with EEG, in adults with epilepsy.

Plain-language title generated from the registry record
Registry title: Ear-Seizure Detection (EarSD) Study

Key facts

Where
Worcester, United StatesSee the 2 sites

Where in United States

  • Ummmc-Memorial CampusWorcester, United StatesTaking people
  • Ummmc-University CampusWorcester, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Felicia Chu
Trial code
NCT06598189
Record updated
14 October 2026
Original description
The proposed study is an investigator-initiated study that aims to measure the accuracy of a wearable seizure detection and prediction device (Ear-Seizure Detection Device (EarSD)) by simultaneous recording with conventional video-EEG (Electroencephalogram) on patients with epileptic seizures in the Epilepsy Monitoring Unit of the hospital.Read full original descriptionShow less

Real-time Seizure Detection, Classification, and Prediction Using a Low-Cost Low-Burden Ear-worn System

The proposed study is an investigator-initiated study that aims to measure the accuracy of a wearable seizure detection and prediction device (Ear-Seizure Detection Device (EarSD)) by simultaneous recording with conventional video-EEG (Electroencephalogram) on patients with epileptic seizures in the Epilepsy Monitoring Unit of the hospital.

Inclusion: Age ≥ 18 years; Patients admitted to UMass Memorial Epilepsy Monitoring Unit (EMU) for long term video-EEG monitoring as part of standard care of both focal and generalized epilepsy; Willing to wear the wearable device; Ability to provide informed consent.

Exclusion: Children (Age 0-17); Subjects wearing other ear devices such as hearing aids; Inability or unwillingness to provide informed consent; Irritation of the skin where the device is to be placed; Patients with intracranial electrodes placement; Prisoners; Cognitive impaired individuals; Pregnant Women.

ClinicalTrials.gov NCT06598189