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:
2025-12-25 @ 4:23 AM
Ignite Modification Date:
2025-12-25 @ 4:23 AM
NCT ID:
NCT05396820
Eligibility Criteria:
Inclusion Criteria:
* Healthy subjects (who do not have self-reported neurological disorders)
* Subjects who have signed an informed consent (who have a good command of French)
* Subjects affiliated with or receiving social security benefits
Exclusion Criteria:
* Psychiatric history obtained through physician questioning: individuals with mental retardation or severe impairment of cognitive, behavioral, or emotional function that precludes understanding the protocol and signing informed consent
* Neurological history (epilepsy, stroke, surgeries performed on the brain or spinal cord, and history of neurological diseases affecting motor skills and sensation)
* Subjects who are unable to receive informed information (dementia, hearing problems, poor French proficiency, etc.)
* Contraindications to MST (epilepsy, intracranial metal foreign bodies, hearing aids or cochlear implants)
* Taking psychotropic medications
* Persons under guardianship or conservatorship
* Pregnant and nursing women
* Subjects with pacemakers
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT05396820
Study Brief:
Protocol Section:
NCT05396820