Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 5:55 PM
Ignite Modification Date:
2025-12-24 @ 5:55 PM
NCT ID:
NCT02788968
Eligibility Criteria:
Inclusion Criteria:
* Healthy and educated adolescents aged 11-15 years
* boy or girl
* French mother tongue
* Handedness : right
* Having been informed by the teen booklet and given its written consent, and whose parents or legal guardian will be ( a) signed the informed consent sheet of the protocol
* Medical examinations , neurological, neuroradiological norma
or
* All healthy young adults aged 19-25 years at university level or in the workforce
* man or woman
* Level ≥ 12 years of study (bachelor level )
* Native language: French
* Handedness : right
* Signing of the informed consent of the protocol
* Medical examinations , neurological, neuroradiological norma
Exclusion Criteria:
* Does not meet the targeted age groups
* Presents against -indications to MRI (severe claustrophobia , foreign bodies cons -indicated )
* This chronic intake of alcohol or drugs
* Cognitive disorders who could testify sudden onset of a stroke ; a history of head injury with loss of consciousness for more than 1 hour , or encephalitis
* A neurological chronic condition , psychiatric, endocrine , hepatic and infectious
* Major disease history (diabetes, chronic lung disease, heart disorder, metabolic , hematologic , endocrine or immunological severe, cancer)
* A medication that may interfere with brain imaging measures ( psychotropics, hypnotics, anxiolytics , neuroleptics, anti -Parkinson , benzodiazepines, anti-inflammatory drugs , antiepileptics, antihistamines , analgesics and muscle relaxants central ) .
* Manual predominantly left (after the first phone call with the contact person of CYCERON ; see section 9.1)
* Color Blindness
* Inability to submit the study for geographical or psychiatric reasons
* Pregnant and lactating women
The following criteria are specific to the adolescent group :
* Has pervasive developmental disorders and / or acquisitions identified by parents or legal guardian and (or ) the teachers
* Parents or legal guardian are not affiliated to a system of social security
* Unaccompanied by parent (s) (s) or legal guardian during the visit to CYCERON center
The following criteria are specific to the group of young adults :
* Non- affiliated to a social security scheme
* Be protected adult
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
11 Years
Maximum Age:
25 Years
Study:
NCT02788968
Study Brief:
Protocol Section:
NCT02788968