Assessment of Transcultural Psychotherapy in Child Major Depressive Disorder (EDPT-ADOS)
Major Depressive Disorder
About this trial
This is an interventional supportive care trial for Major Depressive Disorder focused on measuring Transcultural psychotherapy, migrant, child, adolescent, Depressive Disorder, psychiatric care, mixed studies, bayesian design, qualitative study, Randomized Controlled Trial
Eligibility Criteria
Inclusion Criteria:
- Be a child aged or an adolescent aged 6-20 years-old (this may be a declaratory age at the time of the consultation or based on a document for a residence request if no other identity documents are available)
- Be a first or second-generation migrant (born abroad or born from at least one parent who is born abroad)
- Have a psychological and/or psychiatric follow-up by a first-line care
- Have been referred for transcultural psychotherapy by their first line care to treat depression resistant to standard management.
Present a depression according to the clinician who proposes the transcultural treatment (first line therapist), based on usual as well as cultural symptoms criteria of the below list:
- Sadness
- Diminish interest or pleasure in most of the usual activities
- Insomnia or hypersomnia
- Psychomotor agitation
- Asthenia, loss of energy
- Feeling of worthlessness or excessive guilt
- Recurrent throughs of death
- School problems (school failure, drop in grades, aggressivity with adult, school refusal…)
- Mutism, and selective mutism
- Runaways
- Aggressivity
- Impulsivity
- Violence and delinquency
- Conflicts with parents and adults from the community
- Exclusion from family
- Somatic pains
- Massive separation anxiety
- Regressive symptoms - loosing of an already acquired function such as speech, walk, stay alone for a sufficient time in relation to age, manage stress or anxiety for reasonable situations…
- Denial of medical care for a chronic disease with no evident reasons
- Cultural designation such as possessed by a spirit, being a child witch, or other cultural designations
- State of trance The list is not exhaustive, and some other symptoms may be accepted if the first line clinician as well as the referent agree. The patients will be well characterized after inclusion.
- Present a score >= 4 on the iCGI - Severity at inclusion.
- Present transcultural issues confirmed by the referent (usual procedure of indirect pre-selection based on the presentation of the situation by referring physician)
- Have an informed consent signed by both parents/ one parent / tutor / adult patient (cf. 14.1 paragraph)
Exclusion Criteria:
- Patient or family has previously had transcultural psychotherapy
- Patient presents an acute psychiatric disorder which hinders the realization of the transcultural therapy - for example, excited delirium with great psychic disorganization, or high suicidal risk patients. These situations will be excluded during the screening time based on the first line therapist evaluation
- Patient presents an acute somatic disease which may hinder the well organization of the therapy
- Patient addressed for a legal expertise
- Child's/Adolescent's refusal
- Pregnant or breastfeeding (for women for young women of childbearing age)
- Participation in another interventional study
- Patient under guardianship or curatorship
Sites / Locations
- Service de Psychopathologie de l'enfant, de l'adolescent, CHU Avicenne
- Service de médecine interne, unité de consultation transculturelle, CHRU Saint-André (CHU Bordeaux)
- Service de psychiatrie de l'enfant et de l'adolescent, CHRU Gabriel Montpied
- Maison de Solenn, Cochin Hospital
- Secteur 75G23, Centre Médico-psychologique (CMP), GHU PARIS, Maison blanche
- Centre Médico-psychologique, Service Universitaire de Psychiatrie de l'Enfant et de l'Adolescent, Hôpital La Grave, CHU Toulouse
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Transcultural psychotherapy
standard care
In addition to usual care, the participants in the treatment group receive transcultural psychotherapy in the inclusion centers, which consists of 5 sessions every 7 weeks (W6, W13, W20, W27, and W34). During all the research process, participants from both groups continue their usual care provided by the referent medical team outside the inclusion center.
usual care provided by the referent medical team