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NCT06978842Recruiting

Seizure Prediction Using Wearable EEG

A Multicenter Prospective Non-Interventional Pilot Feasibility Trial for Seizure Prediction Using Wearable Electroencephalogram Among Patients With Confirmed Epilepsy

Source: ClinicalTrials.gov · Last updated 26 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This study is a non-interventional clinical trial analyzing EEG recordings from people with epilepsy. Participants wear a comfortable EEG headband at home for several weeks. The goal is to study changes in brain activity that occur before seizures (called "pre-ictal patterns") and to test whether a software algorithm can predict seizures in real-time based on these patterns. No treatments or medications are being tested. The study will help evaluate whether seizure prediction is possible using wearable EEG devices and can support the development of future tools that give patients early warnings before seizures occur.

Status (registry)
Recruiting
Study type
Observational
Enrollment
150 (estimated)
First submitted
30 Apr 2025
Start date
19 Jun 2025
Primary completion date
Mar 2026
Lead sponsor
Dux Healthcare Inc.
Diseases
Epilepsy
NCT number
NCT06978842

What you commit to

  • Study type: Observational
  • Planned participants: 150
  • From 19 Jun 2025 to the primary completion date, Mar 2026
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Scalp conditions or physical characteristics preventing proper device fit.

Other

  • Any technical or logistical challenges that would prevent reliable EEG data collection or compliance with the study protocol.
  • Pregnant or planning a pregnancy during the study.

Who the study is looking for

  • Age: 12 years and older.
  • Diagnosis of epilepsy confirmed by EEG, with at least one seizure captured during EEG monitoring by a trained expert.
  • Seizure frequency ranging from once per day to two over the last three months preceding inclusion.
  • Sufficient cognitive and physical ability (of the participant or caregiver) to comply with the protocol, including device management and data reporting.
  • Access to and familiarity with a smartphone capable of running the study application as tested during screening.
  • Willingness to provide informed consent and adhere to study procedures.

Age in the registry: 12 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Rambam Medical Center
Coordinator of this site? Confirm its status
HaifaIsraelRecruiting
Sheba medical center
Coordinator of this site? Confirm its status
Ramat GanIsraelNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.