Development of a Seizure Detection Algorithm Based on Heart Rate and Movement Analysis
DetecTeppe
1 other identifier
observational
13
1 country
1
Brief Summary
Epilepsy is the 3rd neurological pathology after migraines and dementia syndromes with a high estimate of nearly 600,000 people affected in France. The disease is characterized by the repetition of epileptic seizures on the one hand, but also by the cognitive, behavioral, psychological and social consequences of this condition, especially when the epileptic disease is not stabilized. Epileptic patients feel a great deal of stress due to the unpredictability of the occurrence of seizures. Seizure detection is of great interest to bioinformatics researchers and to people with epilepsy and their caregivers. Recent advances in physiological sensor technologies and artificial intelligence have opened the possibility of developing systems capable of closely monitoring the frequency of epileptic seizures with a direct impact on therapeutic adaptations. This may eventually allow for seizure prediction and/or "seizure weather" (i.e., seizure forecasting) if there is a particular chronotype of seizure occurrence for a given individual. Currently, few devices have a sufficient level of evidence regarding their effectiveness to be recommended. Those that seem to be the most advanced are those that allow the identification of hypermotor seizures, including tonic-clonic generalized seizures and tonic-clonic secondary generalized focal seizures, mostly occurring at night. The latter represent only a small part of epileptic seizures. The objective of the present study is to build a real life database in order to develop a seizure detection algorithm. The recorded data will be heart rate via ECG and movement data via 9 variables measured on 3 axes x, y, z, with 3 sensors: accelerometer, gyroscope, magnetometer. These data will be collected using a connected patch available on the market (CE marking). At the same time, the patients will benefit from a long term video-EEG examination which will be annotated by the doctors and will be used as a gold standard for the identification of seizures in order to train the algorithm. This more complete base will be used to develop an algorithm previously developed from retrospective data.
Trial Health
Trial Health Score
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participants targeted
Target at below P25 for all trials
Started Jun 2023
1 active site
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 8, 2022
CompletedFirst Posted
Study publicly available on registry
December 5, 2022
CompletedStudy Start
First participant enrolled
June 5, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 24, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 24, 2025
CompletedDecember 17, 2025
February 1, 2025
1.9 years
November 8, 2022
December 9, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
To build a training database under physiological conditions allowing the development of a detection algorithm for generalized and focal epileptic seizures in adults with epilepsy.
Movements will be measured with accelerometer.
Day12
Interventions
The study consists of creating a database to develop an algorithm using machine learning methods.
Eligibility Criteria
The people with epilepsy will be recruited from among the patients/residents being followed for their epilepsy at the Institut La Teppe. Institut La Teppe is a medical and social institution that welcomes people suffering from epilepsy with cognitive deficiencies that can be severe.
You may qualify if:
- Person over 18 years of age - With drug-resistant epilepsy as defined by the International League Against Epilepsy
- Who has at least one recorded seizure with heart rate variation (i.e. tachycardia defined as an increase of 30 bpm or more than 50% over the interictal heart rate and/or bradycardia defined as a heart rate \< 40 bpm or ictal asystole defined as an R-R interval greater than 3 seconds and usually lasting less than 60 seconds)
- Informed about the study and signed a consent to participate in the study (and their legal representative for patients under guardianship)
- Affiliated or beneficiary of a social insurance plan
You may not qualify if:
- Pregnant or breastfeeding woman
- Persons with psychogenic non-epileptic seizures (PNES)
- Person with a history of severe heart disease (myocardial infarction, heart failure, rhythm disorder, severe hypertension)
- Persons with an implantable cardiac device (pacemaker, implantable defibrillator)
- Documented allergy to hydrogel and/or acrylate
- Person benefiting from a legal protection measure other than guardianship or curatorship
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Institut La Teppe
Tain-l'Hermitage, 26600, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- NETWORK
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 8, 2022
First Posted
December 5, 2022
Study Start
June 5, 2023
Primary Completion
April 24, 2025
Study Completion
April 24, 2025
Last Updated
December 17, 2025
Record last verified: 2025-02
Data Sharing
- IPD Sharing
- Will not share