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Clinical Trials/NCT01707576
NCT01707576
Completed
N/A

SCREENING OF ADOLESCENT MENTAL SUFFERING CONSULTANT TO EMERGENCIES, MANAGEMENT AND Later MONITORING

Assistance Publique - Hôpitaux de Paris1 site in 1 country346 target enrollmentFebruary 2010

Overview

Phase
N/A
Intervention
Not specified
Conditions
Depression
Sponsor
Assistance Publique - Hôpitaux de Paris
Enrollment
346
Locations
1
Primary Endpoint
Responses to Self-reported questionnaire on risk behaviors, somatic complaints by adolescents and parents
Status
Completed
Last Updated
10 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
February 2010
End Date
June 2012
Last Updated
10 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

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.

Outcomes

Primary Outcomes

Responses to Self-reported questionnaire on risk behaviors, somatic complaints by adolescents and parents

Time Frame: 10 months

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 Outcomes

  • Post-emergency consultation and reassessment of hetero-ADRS clinician questionnaire(6 months)

Study Sites (1)

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