DepressionDESPERADOSNCT01707576
Screening of Adolescent Mental Suffering
A study testing consultation 10 days later in people with Depression and Adolescent, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.
Trial 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… Read more about this study
- Who is it for?
- Ages 13 to 17 years
- Conditions the study is for
- Depression, Adolescent, Self-report Questionnaire
- What is being tested?
- consultation 10 days later
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 346 participants
- Where
- 1 siteFrance
- Study dates
- Feb 2010to Jun 2012
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 13 to 17 years
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- 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)
Who cannot join
- Young people not reading French.
Trial locations and contacts
1 site in 1 country.
France1 site
Department of paediatric emergencies, Ambroise Paré universitary hospital
Boulogne-Billancourt, Île-de-France Region, 92100
About this study
Official title: SCREENING OF ADOLESCENT MENTAL SUFFERING CONSULTANT TO EMERGENCIES, MANAGEMENT AND Later MONITORING
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.
Read the 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.
- Conditions
- Depression, Adolescent, Self-report Questionnaire
- Being tested
- consultation 10 days later
- Keywords
- Follow-Up Studies, Adolescent, Depressive Disorder, Major/diagnosis, Attempted/prevention & control, Self-report questionnaire, emmergency department, parental perception, Emergency
- Medical subject headings
- Depression, Depressive Disorder, Disease, Emergencies
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
consultation 10 days laterBehavioural
new depression screening
| Study group | Role | What they receive |
|---|---|---|
| screening of adolescent mental suffering. Management | Other | screening of adolescent mental suffering consultant to emergencies. Management and later monitoring Receives: Behavioral: consultation 10 days later |
What is being measured
The primary outcome is the main question the study is designed to answer.
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.
Measured: 10 months
Secondary outcomes (1)
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.
Measured: 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Oct 2012 (estimated)
- Study startFeb 2010
- Primary completionDec 2011
- Study completionJun 2012
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for DepressionStudies of the same condition, open and under way.
- More trials run by Assistance Publique - Hôpitaux de ParisThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Diagnosis
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 346 participants (actual)
Sponsor and investigators
- Lead sponsor
- Assistance Publique - Hôpitaux de Paris
- Sponsor type
- University, hospital or other
- Collaborators
- Pfizer, Fondation de France
- Responsible party
- Sponsor
- Investigators
- Chantal Stheneur, MD, Principal investigator, Ambroise Paré University Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01707576
- Sponsor's protocol ID
- P090103
- Acronym
- DESPERADOS
- Status last verified
- Jan 2010
- First submitted
- 12 Oct 2012
- Last updated
- 4 Apr 2016
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 4 Apr 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- SCREENING OF ADOLESCENT MENTAL SUFFERING CONSULTANT TO EMERGENCIES, MANAGEMENT AND Later MONITORING
- ClinicalTrials.gov ID
- NCT01707576
- Acronym / sponsor ID
- DESPERADOS / P090103
- Conditions
- 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
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 346 participants (actual)
- Lead sponsor
- Assistance Publique - Hôpitaux de ParisUniversity, hospital or other
- Collaborators
- Pfizer, Fondation de France
- Study start
- Feb 2010
- Primary completion
- Dec 2011 (actual)
- Study completion
- Jun 2012 (actual)
- First posted
- 16 Oct 2012 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Diagnosis
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| screening of adolescent mental suffering. Management | Other | Behavioral: consultation 10 days laterscreening of adolescent mental suffering consultant to emergencies. Management and later monitoring |
Who may qualify
- Ages
- 13 to 17 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (1 listed)
- 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)
Key exclusion criteria (1 listed)
- Young people not reading French.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| consultation 10 days laternew depression screening | Behavioural | screening of adolescent mental suffering. Management |
Primary outcome
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.
1 secondary outcome
Post-emergency consultation and reassessment of hetero-ADRS clinician questionnaire
Time frame: 6 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Apr 2016.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Chantal Stheneur, MD principal investigator
Ambroise Paré University Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing consultation 10 days later in people with Depression and Adolescent, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 4 Apr 2016. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Responses to Self-reported questionnaire on risk behaviors, somatic complaints by adolescents and parents (time frame: 10 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Apr 2016; AzTrials last refreshed its copy on 5 Nov 2026.