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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05285059
Other study ID # 69HCL21_1190
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 21, 2023
Est. completion date March 21, 2026

Study information

Verified date March 2023
Source Hospices Civils de Lyon
Contact Marcastel Agathe, PhD
Phone +33 4 27 85 60 40
Email Agathe.marcastel@chu-lyon.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Epileptic children suffer from impairments in various learning and memory tasks. Yet, no study investigated implicit learning in epileptic children. Implicit learning is not only underlying motor skills acquisition, but also social and cognitive ones. Because acquisition of new skills is optimal during childhood, the study of implicit learning mechanism in children is of major importance. The present study will be the first to explore implicit learning mechanisms in children with epilepsy. Implicit learning mechanisms can be preserved or altered.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date March 21, 2026
Est. primary completion date March 21, 2026
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 8 Years to 14 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Behavioral:
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.

Locations

Country Name City State
France 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

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Response time Response time (in milliseconds) recorded during the ASRT task The day of the inclusion
Primary Response accuracy recorded during the ASRT task Response accuracy (percentage of correct answers) The day of the inclusion
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