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 @ 4:55 AM
Ignite Modification Date:
2025-12-25 @ 4:55 AM
NCT ID:
NCT07207018
Eligibility Criteria:
Inclusion Criteria:
* Children aged between 7 and 17 years living in the family home;
* Having been exposed to a traumatic event (TE) in the last 3 months;
* Exhibiting at least one symptom on the Child Post-Traumatic Stress Checklist (CPC);
* Having at least one of the two parents available to participate in the intervention; and
* Having a good command of French, both orally and in writing.
* No participation in other therapeutic interventions aimed at treating traumatic stress symptoms is allowed during the inclusion period.
Exclusion Criteria:
* Parents and/or children in acute and severe emotional distress and/or in a suicidal crisis. During the recruitment interview and signing of the consent letter, the principal investigator will ensure that the volunteer participants are not in acute suicidal crisis or in severe emotional distress requiring urgent care, which would prevent them from participating in a five-session intervention (CFTSI). This emotional distress assessment will be a clinical evaluation based on the clinician's judgment.
* Child in foster care or in the process of being placed.
* Suspected maltreatment or abuse of any kind by the parents.
* Child and/or parent with a known and/or documented intellectual disability.
* Absence of consent from either of the child's parents or the child's non-agreement to participate (appropriately obtained according to the child's developmental age, taking the time to explain the procedure and intervention to the child).
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
7 Years
Maximum Age:
17 Years
Study:
NCT07207018
Study Brief:
Protocol Section:
NCT07207018