Screening of Adolescent Mental Suffering
DESPERADOS
SCREENING OF ADOLESCENT MENTAL SUFFERING CONSULTANT TO EMERGENCIES, MANAGEMENT AND Later MONITORING
1 other identifier
interventional
346
1 country
1
Brief Summary
The primary purpose is to estimate the prevalence of depression and subsyndromal states among adolescents 13 to 17 years consulting to hospital emergency rooms for any reason, for they are another way of tracking this suffering, as they host many troubled teens at once for health problems and accidents sometimes iterative, reflecting their risk behaviour. Secondary purposes are to assess the feasibility and desirability of a post-emergency medical consultation for adolescents who scored high on a self-administered questionnaire, and to assess the impact of this approach by later monitoring.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable depression
Started Feb 2010
Typical duration for not_applicable depression
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2012
CompletedFirst Submitted
Initial submission to the registry
October 12, 2012
CompletedFirst Posted
Study publicly available on registry
October 16, 2012
CompletedApril 4, 2016
January 1, 2010
1.8 years
October 12, 2012
April 1, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Responses to Self-reported questionnaire on risk behaviors, somatic complaints by adolescents and parents
A self-questionnaire ADRS (Adolescent Depression Rating Scale) will be asked to all adolescents to complete. Also the other questions will be answered by them concenrning somatisations and risk behaviors. Parents respond in the same time a self questionnaire.
10 months
Secondary Outcomes (1)
Post-emergency consultation and reassessment of hetero-ADRS clinician questionnaire
6 months
Other Outcomes (1)
Revaluation after one year
6 months
Study Arms (1)
screening of adolescent mental suffering. Management
OTHERscreening of adolescent mental suffering consultant to emergencies. Management and later monitoring
Interventions
new depression screening
Eligibility Criteria
You may qualify if:
- Adolescents over the age of 13 to 17 years when passing emergency whatever the reason for consultation (surgical or medical, including attempted suicide or psychological problem)
You may not qualify if:
- Young people not reading French.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Assistance Publique - Hôpitaux de Parislead
- Pfizercollaborator
- Fondation de Francecollaborator
Study Sites (1)
Department of paediatric emergencies, Ambroise Paré universitary hospital
Boulogne-Billancourt, Île-de-France Region, 92100, France
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Chantal Stheneur, MD
Ambroise Paré University Hospital
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 12, 2012
First Posted
October 16, 2012
Study Start
February 1, 2010
Primary Completion
December 1, 2011
Study Completion
June 1, 2012
Last Updated
April 4, 2016
Record last verified: 2010-01