Screening of Adolescent Mental Suffering (DESPERADOS)
Primary Purpose
Depression, Adolescent, Self-report Questionnaire
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
consultation 10 days later
Sponsored by

About this trial
This is an interventional diagnostic trial for Depression focused on measuring Follow-Up Studies, Adolescent, Depressive Disorder, Major/diagnosis, Attempted/prevention & control, Self-report questionnaire, emmergency department, parental perception, Emergency
Eligibility Criteria
Inclusion Criteria:
- 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)
Exclusion Criteria:
- Young people not reading French.
Sites / Locations
- Department of paediatric emergencies, Ambroise Paré universitary hospital
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
screening of adolescent mental suffering. Management
Arm Description
screening of adolescent mental suffering consultant to emergencies. Management and later monitoring
Outcomes
Primary Outcome Measures
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.
Secondary Outcome Measures
Post-emergency consultation and reassessment of hetero-ADRS clinician questionnaire
Actual presence of adolescents suspected of depression at the post-emergency consultation and reassessment of their state using the hetero-ADRS-clinician questionnaire.
Full Information
NCT ID
NCT01707576
First Posted
October 12, 2012
Last Updated
April 1, 2016
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Pfizer, Fondation de France
1. Study Identification
Unique Protocol Identification Number
NCT01707576
Brief Title
Screening of Adolescent Mental Suffering
Acronym
DESPERADOS
Official Title
SCREENING OF ADOLESCENT MENTAL SUFFERING CONSULTANT TO EMERGENCIES, MANAGEMENT AND Later MONITORING
Study Type
Interventional
2. Study Status
Record Verification Date
January 2010
Overall Recruitment Status
Completed
Study Start Date
February 2010 (undefined)
Primary Completion Date
December 2011 (Actual)
Study Completion Date
June 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Pfizer, Fondation de France
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
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.
Detailed Description
This is a multicenter longitudinal survey in three emergency centers in Ile-de-France, with 2 periods of daily collection and comprehensive three weeks spread over one year, followed by a remote evaluation.
The project is as follows:
Phase A :
- Evaluation of the prevalence: systematic execution of self-administered questionnaire by all adolescents consulting, night and day in each center.
Phase B :
For adolescents whose outcome questionnaire exceed 4, a post-emergency consultation will be proposed within 15 days.
Telephone survey, 12 months after the passage of emergency every teenager who completed self-administered questionnaire and presenting himself to the post-emergency consultation. This survey will aim to assess the psychological status of adolescents and the impact of any specific treatment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Adolescent, Self-report Questionnaire
Keywords
Follow-Up Studies, Adolescent, Depressive Disorder, Major/diagnosis, Attempted/prevention & control, Self-report questionnaire, emmergency department, parental perception, Emergency
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
346 (Actual)
8. Arms, Groups, and Interventions
Arm Title
screening of adolescent mental suffering. Management
Arm Type
Other
Arm Description
screening of adolescent mental suffering consultant to emergencies. Management and later monitoring
Intervention Type
Behavioral
Intervention Name(s)
consultation 10 days later
Intervention Description
new depression screening
Primary Outcome Measure Information:
Title
Responses to Self-reported questionnaire on risk behaviors, somatic complaints by adolescents and parents
Description
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.
Time Frame
10 months
Secondary Outcome Measure Information:
Title
Post-emergency consultation and reassessment of hetero-ADRS clinician questionnaire
Description
Actual presence of adolescents suspected of depression at the post-emergency consultation and reassessment of their state using the hetero-ADRS-clinician questionnaire.
Time Frame
6 months
Other Pre-specified Outcome Measures:
Title
Revaluation after one year
Description
Revaluation after 1 year of the teenagers who come back to visit.
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
13 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
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)
Exclusion Criteria:
Young people not reading French.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chantal Stheneur, MD
Organizational Affiliation
Ambroise Paré University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of paediatric emergencies, Ambroise Paré universitary hospital
City
Boulogne Billancourt
State/Province
Ile de France
ZIP/Postal Code
92100
Country
France
12. IPD Sharing Statement
Learn more about this trial
Screening of Adolescent Mental Suffering
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