About this trial
It is a comparative monocentric study with longitudinal follow-up at 6 months in adolescents aged between 11 years and 17 years inclusive admitted to complete hospitalization either for suicidal behaviors or for other psychiatric causes. The objective is to explore the experiences of hospitalized adolescents regarding hospitalization, as well as their perceptions of the factors involved in their remission and their experience of the traumatic event(s) if they have been exposed.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age between 11 and 17 years inclusive
Admitted for full-time psychiatric hospitalization
Obtaining consent from at least one of the adolescent's legal representatives and the adolescent's personal assent
Disqualifiers
None
Trial design
Parallel
Treatments tested in this trial
Blood samples
Biological/VaccineA blood test will be carried out during the inclusion visit, on site, with collection of the time of completion, the last food samples and tobacco consumption. A 2.5 mL Paxgene® tube for whole blood RNA and a 5 mL dry tube for serum will be collected.
genetic analysis
GeneticIf consent for genetic analyses is obtained, a 4.5 mL EDTA tube to collect native DNA will be taken during the blood test
Questionnaires and scales
Other intervention* Child Posttraumatic Checklist (CPC) * Life Event Checklist (LEC-5) * Posttraumatic CheckList-5 * K-SADS * Affective Reactivity Index (ARI) * Child Youth Resilience Measure * Adverse Childhood Experiences International Questionnaire (ACE-IQ) * Metacognitions Questionnaire (MCQ-A) * Cognitive Emotion Regulation Questionnaire (CERQ) * Adolescent Dissociative Experience Scale (A-DES) * Behavioral Rating Inventory of Executive Function Self-Report (BRIEF-2)
Treatment groups
Trial outcomes
Primary outcomes
CPC Questionnaire child version
This questionnaire evaluates the symptoms of PTSD and their frequency in children aged 7 to 18 years, following a traumatic event. Completion time is 15-20 minutes and the total score can range from 0 (no symptoms) to 84 (maximum symptoms) for symptom intensity and from 0 (no functional impact) to 24 (maximum functional impact) for functional impairment. The scale will be administered by a clinician (psychologist or psychiatrist for children and adolescents).
Secondary outcomes
CPC questionnaire parents version
This questionnaire evaluates by parents the symptoms of their children in PTSD and their frequency in children aged 7 to 18 years, following a traumatic event. Completion time is 15-20 minutes and the total score can range from 0 (no symptoms) to 84 (maximum symptoms) for symptom intensity and from 0 (no functional impact) to 24 (maximum functional impact) for functional impairment. The scale will be administered by a clinician or self-administered (psychologist or psychiatrist for children and adolescents).
Questionnaire Life Event Checklist (LEC-5)
The Life Event Checklist version of DSM-5 (19) consists of a list of 16 potentially trauma events in reference to criterion 1 of PTSD from DSM-5. It does not generate a total score but allows for a record of trauma events if they have occurred or not.
Schedule for Affective Disorders and Schizophrenia for school-age children (KSADS) full-life version
It is a hetero-administered questionnaire that allows for the screening and diagnosis of psychiatric and neurodevelopmental disorders in children and adolescents.
Post-traumatic Stress Disorder Checklist for DSM-5 (PCL-5)
The PCL-5 (23) is composed of 20 items that correspond to the 20 PTSD criteria detailed in the DSM-5, and contains four subscales corresponding to the four clusters of symptoms in the DSM-5: intrusion phenomena, avoidance, negative alterations of cognition and mood, and increase in hyperactivity and reactivity. The score can range from 0 (no symptoms) to 80 (maximum symptoms). PCL-5 is a self-administered questionnaire that can also be administered with the help of a clinician.
Locations
Sponsors and contacts
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