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 @ 10:55 PM
Ignite Modification Date:
2025-12-24 @ 10:55 PM
NCT ID:
NCT04547569
Eligibility Criteria:
Inclusion Criteria:
* Right-handed subjects
* Subjects fluent in French
* Signed informed consent
* Affiliation to or beneficiary of a Social Security scheme
Exclusion Criteria:
* Left-handed subjects
* Criteria for contraindications to protocol fMRI scans
* Existence of a severe general condition: cardiac, respiratory, hematological, renal, hepatic, cancerous.
* Hearing, language (including dyslexia), neurological or psychiatric disorders.
* Participation in other ongoing intervention research protocols with exclusionary period or within the previous week
* Drug treatment likely to modulate brain activity: benzodiazepines, antidepressants, neuroleptics, lithium, etc.
* Protected persons referred to in articles L1121 5 to L1121 8 of the French CSP:
* Pregnant women, parturients, nursing mothers,
* Persons deprived of liberty by a judicial or administrative decision,
* Persons under psychiatric care,
* Individuals admitted to a health or social institution for purposes other than research,
* Minors,
* Persons over the age of majority who are subject to a legal protection measure or who are unable to express their consent
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
35 Years
Study:
NCT04547569
Study Brief:
Protocol Section:
NCT04547569