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DepressionDESCOLNCT03904784

School Withdrawal in Adolescents

An observational study of Depression and Anxiety Disorders, run by Centre Hospitalier Intercommunal Creteil at 1 site in France.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

The aim of the study is to evaluate the impact of the outpatient ambulatory child psychiatric care system on the functioning of anxio-depressive adolescents in school retreat by describing the modalities of individual psychic functioning. Read more about this study

Who is it for?
Ages 12 to 17 years
What is being tested?
school withdrawal teenagers
How many people
8 participants
Where
1 siteFrance
Study dates
21 Mar 2019to 12 Feb 2021
Phase
Observational
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 12 to 17 years
  • All sexes
  • Child

Study population: teenagers between 12 and 17 years who are anxio-depressive and school retreat

Who may be able to join

  • New patients in the sector with a problem of school withdrawal previously educated in ordinary medium without MDPH file (Departmental House of Disabled People).
  • Young people out of school: school attendance less than 50% of school time for one month (absent at least half of school time)
  • Clinical diagnosis according to the International Classification of Diseases 10 (ICD 10): F32 (depressive episodes), F33 (recurrent depressive disorder), F40 (phobic anxiety disorders), F41 (other anxiety disorders), F42 (obsessive-compulsive disorders), F43 (reaction to severe stressor, and adjustment disorders), F45 (somatoform disorder), F48 (other neurotic disorders), F90 to F98 Behavioral and emotional disorders usually occurring during childhood and adolescence
  • Accepting to participate in the clinical research device

Who cannot join

  • Other psychiatric diagnoses (schizophrenia, BDA (acute delirious puff), TED (Invasive Disorder of Development)).
  • Intellectual deficit proved
  • Education in SEGPA (Section of General and Adapted Professional Education) and ULIS (Localized Unit for School Inclusion)
  • Somatic illness preventing attendance at a school
  • Refusal to participate in the study

Trial locations and contacts

1 site in 1 country.

France1 site
  • 1er secteur de psychopathologie de l'enfant et de l'adolescent du Val de Marne

    Champigny-sur-Marne, 94500

Other trials in France

About this study

Official title: School Withdrawal in Adolescents: Impact of the Ambulatory Child Psychiatry Therapeutic Device. Prospective Study

The aim of the study is to evaluate the impact of the outpatient ambulatory child psychiatric care system on the functioning of anxio-depressive adolescents in school retreat by describing the modalities of individual psychic functioning.

Read the detailed description

This research project concerns adolescent patients aged 12 to 17, a period of life towards psychic individualization and autonomy. It is part of an outpatient child psychiatry sector that is concerned with the multidisciplinary and institutional dimension of the care provided. These are part of a long-term patient care dynamic. It is a therapeutic accompaniment of the young person and his entourage, especially parents.

The care is integrative and multidisciplinary (psychiatrist, psychologist, educator, psychomotor, nurse). The care project is done after team discussion, several points are taken into account (clinical evaluation, demand analysis, transfer, study of different psychic movements, family dynamics). The eyes are crossed and the various references (psychodynamic, psychoanalytic, systemic). The family consultations that are always present can be associated with the individual care of the young person, and always link with the analysis of the different institutional movements. This takes place especially at the time of the weekly clinical summaries where the clinical situations of concern are evoked to allow a cross reading and multidisciplinary.

The reflection, the exchange between the various stakeholders allow to weave an institutional mesh containing. Thanks to this system, young people and their families can experience a continuous and solid relationship.

The sector is also part of a very valuable network work with the various partners involved in the daily life of the young person and their family (school institution, social services ...).

This research is intended to be as close as possible to the care we provide and is integrated into a global work whose main interest is that of the patient.

Being tested
school withdrawal teenagers
Medical subject headings
Depression, Anxiety Disorders, Obsessive-Compulsive Disorder, Mental Disorders, Somatoform Disorders, Neurotic Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • school withdrawal teenagersBehavioural

    The teenagers will have 4 interview with medical team alone or with his familly in order to have questionnaries, schools reports, psychological evaluation.

Study groups in NCT03904784
Study groupRoleWhat they receive
School withdrawal teenagersThe study is based on questionnaries, interview with teenagers and/or their familly
Receives: Behavioral: school withdrawal teenagers

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. psychological assessment

    interview of the teenager with a psychologist

    Measured: 18 months

Secondary outcomes (2)
  1. school report

    change in school level

    Measured: 18 months

  2. familly questionnary

    interview of the family with a psychologist

    Measured: 18 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Apr 2019
  2. Study start21 Mar 2019
  3. Primary completion12 Feb 2021
  4. Study completion12 Feb 2021

Why it stopped: During the pandemic covid-19 the school is not in the classroom The study cannot continue

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
8 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03904784
Sponsor's protocol ID
DESCOL
Acronym
DESCOL
Status last verified
Jun 2021
First submitted
4 Apr 2019
Last updated
20 Sep 2021
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Depression and Anxiety Disorders, run by Centre Hospitalier Intercommunal Creteil 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 4 inclusion and 5 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: stopped early, as of the sponsor's last update on 20 Sep 2021. 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 was stopped early (reason given: During the pandemic covid-19 the school is not in the classroom The study cannot continue). Results are not available in the source record.

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?

psychological assessment (time frame: 18 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 20 Sep 2021.

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