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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03904784
Other study ID # DESCOL
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date March 21, 2019
Est. completion date February 12, 2021

Study information

Verified date June 2021
Source Centre Hospitalier Intercommunal Creteil
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical 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.


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.


Recruitment information / eligibility

Status Terminated
Enrollment 8
Est. completion date February 12, 2021
Est. primary completion date February 12, 2021
Accepts healthy volunteers
Gender All
Age group 12 Years to 17 Years
Eligibility Inclusion Criteria: - 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 Exclusion Criteria: - 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

Study Design


Intervention

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

Locations

Country Name City State
France 1er secteur de psychopathologie de l'enfant et de l'adolescent du Val de Marne Champigny-sur-Marne

Sponsors (2)

Lead Sponsor Collaborator
Centre Hospitalier Intercommunal Creteil University of Paris 5 - Rene Descartes

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary psychological assessment interview of the teenager with a psychologist 18 months
Secondary school report change in school level 18 months
Secondary familly questionnary interview of the family with a psychologist 18 months
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