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EpilepsyIMPLICITNCT05285059

Implicit Learning in Epileptic Children

An observational study of Epilepsy, run by Hospices Civils de Lyon at 3 sites in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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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. Read more about this study

Who is it for?
Ages 8 to 14 yearsHealthy volunteers can take part
Conditions the study is for
Epilepsy
What is being tested?
ASRT task
How many people
40 participants
Where
3 sitesFrance
Study dates
21 Mar 2023to 21 Mar 2027
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 8 to 14 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Study population: This study focuses on children with epilepsy.

Who may be able to join

  • 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

Who cannot join

  • Neurological impairments unrelated to epilepsy
  • Psychiatric impairments unrelated to epilepsy
  • Developmental impairments unrelated to epilepsy

Trial locations and contacts

3 sites in 1 country. Contact the study team or a site near you to ask about taking part.

France3 sites, 3 recruiting
  • Agathe Marcastel, PhD

    Bron, Bron, 69675

    Marcastel Agathe, PhD, +33 4 27 85 60 40, Agathe.marcastel@chu-lyon.fr

    Recruiting
  • Dezso Nemeth

    Bron, Bron, 69675

    Nemeth Dezso, Pr, +33 4 81 10 66 04, dezso.nemeth@univ-lyon1.fr

    Not yet recruiting
  • Service d'Epileptologie Clinique, des Troubles du sommeil et de Neurologie fonctionnelle de l'enfant, à Hôpital Femme Mère et Enfant,

    Bron

    MARCASTEL Agathe

    Recruiting

Other trials in France

About this study

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.

Conditions
Epilepsy
Being tested
ASRT task
Keywords
Epilepsy,, children,, implicit learning
Medical subject headings
Epilepsy

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ASRT taskBehavioural

    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.

Study groups in NCT05285059
Study groupRoleWhat they receive
Patients8- to 14-years-old children with epilepsy
Receives: Behavioral: ASRT task
Control8- to 14-years-old children without neurological, psychiatric, or developmental impairments
Receives: Behavioral: ASRT task

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Response time

    Response time (in milliseconds) recorded during the ASRT task

    Measured: The day of the inclusion

  2. Response accuracy recorded during the ASRT task

    Response accuracy (percentage of correct answers)

    Measured: The day of the inclusion

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Mar 2022
  2. Study start21 Mar 2023
  3. Primary completion21 Mar 2027 (estimated)
  4. Study completion21 Mar 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
40 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05285059
Sponsor's protocol ID
69HCL21_1190
Acronym
IMPLICIT
Status last verified
May 2026
First submitted
7 Mar 2022
Last updated
7 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Epilepsy, run by Hospices Civils de Lyon at 3 sites in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 7 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Marcastel Agathe, PhD (+33 4 27 85 60 40, Agathe.marcastel@chu-lyon.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Response time (time frame: The day of the inclusion). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 May 2026.

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