- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05285059
Implicit Learning in Epileptic Children (IMPLICIT)
Study Overview
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Marcastel Agathe, PhD
- Phone Number: +33 4 27 85 60 40
- Email: Agathe.marcastel@chu-lyon.fr
Study Contact Backup
- Name: Nemeth Dezso, Pr
- Phone Number: +33 4 81 10 66 04
- Email: dezso.nemeth@univ-lyon1.fr
Study Locations
-
-
-
Bron, France, 69675
- Recruiting
- Agathe Marcastel, PhD
-
Contact:
- Marcastel Agathe, PhD
- Phone Number: +33 4 27 85 60 40
- Email: Agathe.marcastel@chu-lyon.fr
-
Bron, France, 69675
- Not yet recruiting
- Dezso Nemeth
-
Contact:
- Nemeth Dezso, Pr
- Phone Number: +33 4 81 10 66 04
- Email: dezso.nemeth@univ-lyon1.fr
-
Bron, France
- Recruiting
- Service d'Epileptologie Clinique, des Troubles du sommeil et de Neurologie fonctionnelle de l'enfant, à Hôpital Femme Mère et Enfant,
-
Contact:
- MARCASTEL Agathe
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- For Patient group only: Children with epilepsy
- 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:
- Neurological impairments unrelated to epilepsy
- Psychiatric impairments unrelated to epilepsy
- Developmental impairments unrelated to epilepsy
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Patients
8- to 14-years-old children with epilepsy
|
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
|
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. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Response time
Time Frame: The day of the inclusion
|
Response time (in milliseconds) recorded during the ASRT task
|
The day of the inclusion
|
Response accuracy recorded during the ASRT task
Time Frame: The day of the inclusion
|
Response accuracy (percentage of correct answers)
|
The day of the inclusion
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Marcastel Agathe, PhD, Service d'Epileptologie Clinique, des Troubles du sommeil et de Neurologie fonctionnelle de l'enfant - Hôpital Femme Mère Enfant
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 69HCL21_1190
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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