- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06489912
Overview of the Mental Health of Adolescents in Therapeutci, Educational and Pedagogical Facilities in France (PsyPreDi)
June 8, 2026 updated by: University Hospital, Rouen
Etat Des Lieux de la santé Mentale Des Adolescents Suivis Par Les Dispositifs ITEP en France
Assess the prevalence of various psychiatric disorders in adolescents aged 12 to 16 receiving support from therapeutic, educational and pedagogical institutes.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
200
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Priscille Gerardin, Pr
- Phone Number: 02.32.88.56.96
- Email: priscille.gerardin@chu-roue.fr
Study Locations
-
-
-
Besançon, France
- Recruiting
- CHU Bourgogne Franche Comté
-
Contact:
- Lauriane VUILLIEZ
- Phone Number: 0232888990
- Email: cecile.pourcher@chu-rouen.fr
-
Rouen, France
- Recruiting
- CHU Rouen
-
Contact:
- Priscille GERARDIN
- Phone Number: +33 0232888990
- Email: cecile.pourcher@chu-rouen.fr
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
This is a prospective, multicentric, national cohort, including adolescents aged 12 to 16 consecutively, who have been in a French-speaking, voluntary DITEP for at least 15 days, and whose parents have given their consent.
This choice was motivated by the fact that this is the age group most represented in Therapeutic, Educatuional and Pedagogical Institutes
Description
Inclusion Criteria:
- Adolescent aged 12 to 16
- In a DITEP for at least 15 days
- Minor who has been informed and has not objected to the research (according to his/her capacity)
- At least one person exercising parental authority who has read and understood the information note and has not objected to the research OR
- For a minor under guardianship: legal representative who has read and understood the information note and has not objected to the research.
Exclusion Criteria:
- Minor and/or person(s) exercising parental authority who do not understand French
- Holder of parental authority opposed to the search
- Minor opposed to search
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Presence of psychiatric disorders
Time Frame: Inclusion
|
assessed according to DSM-5 by K- SADS-PL
|
Inclusion
|
|
nature of psychiatric disorders
Time Frame: Inclusion
|
assessed according to DSM-5 by K- SADS-PL
|
Inclusion
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Describe the psychological characteristics of adolescents aged 12 to 16
Time Frame: Inclusion
|
Traumatisms
|
Inclusion
|
|
Describe the psychological characteristics of adolescents aged 12 to 16
Time Frame: Inclusion
|
Attachement
|
Inclusion
|
|
Describe the psychological characteristics of adolescents aged 12 to 16
Time Frame: Inclusion
|
Toronto Alexithymia Scale
|
Inclusion
|
|
Describe the psychological characteristics of adolescents aged 12 to 16
Time Frame: Inclusion
|
Empathy scale
|
Inclusion
|
|
Describe the psychological characteristics of adolescents aged 12 to 16
Time Frame: Inclusion
|
Impulsivity scale
|
Inclusion
|
|
Describe the psychological characteristics of adolescents aged 12 to 16
Time Frame: Inclusion
|
Reflective self esteem scale
|
Inclusion
|
|
Describe the psychological characteristics of adolescents aged 12 to 16
Time Frame: Inclusion
|
Abbreviated-diagnostic interview for borderlines
|
Inclusion
|
|
Describe the psychological characteristics of adolescents aged 12 to 16
Time Frame: Inclusion
|
Hostility
|
Inclusion
|
|
Describe the psychological characteristics of adolescents aged 12 to 16
Time Frame: Inclusion
|
Buss Durkee Hostility Inventory
|
Inclusion
|
|
Describe the psychological characteristics of adolescents aged 12 to 16
Time Frame: Inclusion
|
Mentoring assessed by Reflective Functioning Questionnaire
|
Inclusion
|
|
Describe the psychological characteristics of adolescents aged 12 to 16
Time Frame: Inclusion
|
Coping strategies assessed by Adolescent Coping Scale
|
Inclusion
|
|
Describe the psychological characteristics of adolescents aged 12 to 16
Time Frame: Inclusion
|
Risk behaviour assessed by COLUMBIA-SUICIDE SEVERITY RATING SCALE
|
Inclusion
|
|
cognitive abilities
Time Frame: Inclusion
|
Raven's Matrix
|
Inclusion
|
|
Adverse exepriences
Time Frame: Inclusion
|
Adverse Child Experiences
|
Inclusion
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 20, 2024
Primary Completion (Estimated)
December 31, 2026
Study Completion (Estimated)
December 31, 2026
Study Registration Dates
First Submitted
June 28, 2024
First Submitted That Met QC Criteria
June 28, 2024
First Posted (Actual)
July 8, 2024
Study Record Updates
Last Update Posted (Actual)
June 10, 2026
Last Update Submitted That Met QC Criteria
June 8, 2026
Last Verified
June 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2022/0282/OB
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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