NCT01707576

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
346

participants targeted

Target at P75+ for not_applicable depression

Timeline
Completed

Started Feb 2010

Typical duration for not_applicable depression

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2010

Completed
1.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2011

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2012

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

October 12, 2012

Completed
4 days until next milestone

First Posted

Study publicly available on registry

October 16, 2012

Completed
Last Updated

April 4, 2016

Status Verified

January 1, 2010

Enrollment Period

1.8 years

First QC Date

October 12, 2012

Last Update Submit

April 1, 2016

Conditions

Keywords

Follow-Up StudiesAdolescentDepressive Disorder, Major/diagnosisAttempted/prevention & controlSelf-report questionnaireemmergency departmentparental perceptionEmergency

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

OTHER

screening of adolescent mental suffering consultant to emergencies. Management and later monitoring

Behavioral: consultation 10 days later

Interventions

new depression screening

screening of adolescent mental suffering. Management

Eligibility Criteria

Age13 Years - 17 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

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

Study Sites (1)

Department of paediatric emergencies, Ambroise Paré universitary hospital

Boulogne-Billancourt, Île-de-France Region, 92100, France

Location

MeSH Terms

Conditions

DepressionDepressive DisorderDiseaseEmergencies

Interventions

Referral and Consultation

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehaviorMood DisordersMental DisordersPathologic ProcessesPathological Conditions, Signs and SymptomsDisease Attributes

Intervention Hierarchy (Ancestors)

Professional PracticeOrganization and AdministrationHealth Services Administration

Study Officials

  • Chantal Stheneur, MD

    Ambroise Paré University Hospital

    PRINCIPAL INVESTIGATOR

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

Locations