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 @ 3:29 AM
Ignite Modification Date:
2025-12-25 @ 3:29 AM
NCT ID:
NCT04948905
Eligibility Criteria:
Inclusion Criteria:
* Subject must have given written consent
* Subject affiliated or beneficiary of a health insurance plan.
* Adult subjects between 25 and 55 years of age
* Oral and written mastery of the French language
Inclusion criteria for the borderline group:
* Subject diagnosed as having borderline personality disorder according to the DSM IV classification
Exclusion criteria for the borderline group:
* Patients without diagnosis of borderline personality disorder according to the DSM IV classification after taking the SCID II (Structured Clinical Interview for DSM-III-R Axis II Disorders) test
Exclusion criteria for the control group:
* Subjects considered Borderline after taking the SCID II (Structured Clinical Interview for DSM-III-R Axis II Disorders) test
* Subjects with a score above 8 on the HADS questionnaire corresponding to questionable symptomatology for anxiety and depressive symptoms.
General exclusion Criteria:
* Subjects under court protection, guardianship or curatorship
* Subjects for whom it is impossible to give informed information
* Subjects participating in a Category 1 or 2 RIPH in the 3 months prior to the study
* Subject refusing to give written consent
* Presence of known neurological disease
* Pregnant or breastfeeding women
Healthy Volunteers:
True
Sex:
ALL
Study:
NCT04948905
Study Brief:
Protocol Section:
NCT04948905