Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
40 participants
OBSERVATIONAL
2023-03-21
2026-03-21
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patients
8- to 14-years-old children with epilepsy
ASRT task
The ASRT (Alternating Serial Reaction Time) task is a computerized behavioral task measuring implicit learning. This task consists of 20 series of trials lasting 2 minutes each.
In each trial, a stimulus is displayed on the screen in one of the four possible predefined locations. The participant must press a button to indicate the position of the stimulus on the screen. Response content and response time are recorded.
At the end of every trial, the participant can take a break and resume the task whenever ready. The task lasts about 45 to 50 minutes.
Control
8- to 14-years-old children without neurological, psychiatric, or developmental impairments
ASRT task
The ASRT (Alternating Serial Reaction Time) task is a computerized behavioral task measuring implicit learning. This task consists of 20 series of trials lasting 2 minutes each.
In each trial, a stimulus is displayed on the screen in one of the four possible predefined locations. The participant must press a button to indicate the position of the stimulus on the screen. Response content and response time are recorded.
At the end of every trial, the participant can take a break and resume the task whenever ready. The task lasts about 45 to 50 minutes.
Interventions
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ASRT task
The ASRT (Alternating Serial Reaction Time) task is a computerized behavioral task measuring implicit learning. This task consists of 20 series of trials lasting 2 minutes each.
In each trial, a stimulus is displayed on the screen in one of the four possible predefined locations. The participant must press a button to indicate the position of the stimulus on the screen. Response content and response time are recorded.
At the end of every trial, the participant can take a break and resume the task whenever ready. The task lasts about 45 to 50 minutes.
Eligibility Criteria
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Inclusion Criteria
* For Control group only: Children without neurological, psychiatric or developmental impairments
* For both groups: Parent or tutors agreement
* For both groups: Affiliated to French social security
Exclusion Criteria
* Psychiatric impairments unrelated to epilepsy
* Developmental impairments unrelated to epilepsy
8 Years
14 Years
ALL
Yes
Sponsors
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Hospices Civils de Lyon
OTHER
Responsible Party
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Principal Investigators
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Marcastel Agathe, PhD
Role: PRINCIPAL_INVESTIGATOR
Service d'Epileptologie Clinique, des Troubles du sommeil et de Neurologie fonctionnelle de l'enfant - Hôpital Femme Mère Enfant
Locations
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Agathe Marcastel, PhD
Bron, , France
Dezso Nemeth
Bron, , France
Service d'Epileptologie Clinique, des Troubles du sommeil et de Neurologie fonctionnelle de l'enfant, à Hôpital Femme Mère et Enfant,
Bron, , France
Countries
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Central Contacts
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Facility Contacts
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MARCASTEL Agathe
Role: primary
Other Identifiers
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69HCL21_1190
Identifier Type: -
Identifier Source: org_study_id
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