Adolescent Depression Associated With Parental Depression
NCT ID: NCT03811041
Last Updated: 2022-04-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
TERMINATED
NA
80 participants
INTERVENTIONAL
2019-03-28
2021-03-11
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
In children the existence of a parental depression is a significant and recognized risk factor for the development of a depression. It is regularly reported that 30% of adolescents of depressed parents have depression themselves. General Practitioners (GP) have significant access to the depression of adults, potentially parents of teenagers. In fact, 20% of patients in the regular active file of one GP have depression. The primary health care system could provide indirect but voluminous and unprecedented access to the identification of adolescent depression at an early stage from the encounter of depressed parents.
The difficulties of articulation between primary care (PC) and mental health devices are demonstrated. They disrupt the care pathways of adolescents detected in PC, prevention, and may even disturb early detection of depression. An organized joint between the PC and a specialized mental health service for adolescents ("Maison Des Adolescents" MDA) could promote the process of screening and preventing depression of adolescents of depressed parents encountered in PC.
In addition, if the effects of parental depression on adolescents are established, they remain complex and interactive. They vary by age and sex of the child but also the sex of the parent. A concomitant study of adolescent and parent depression will provide data to analyze the prevalence of depressed parent adolescent depression and to define risk or protection factors.
AdoDesP study is a cluster randomised trial (randomisation of the GPs) which compare a group of adolescent with PC articulated with mental health service (MDA) and an other group without articulation (routine cares).
A third group of depressed adolescents will be constituted to analyse parental depression of depressed adolescents.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Paternal Involvement in Psychiatric Care of Adolescents Managed for Depression or Suicide Attempt
NCT03661008
PRimary Prevention Of Depression in Offspring of Depressed Parents
NCT02115880
Efficacity of Psychological Intervention on Reducing the Suicidal Ideations, Depression Level and Improving Reinsertion
NCT03655730
Reaching Out to Adolescents With Depression
NCT01140464
Preventing Depression in the Children of Depressed African American Mothers
NCT00904917
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
DIAGNOSTIC
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
PC articulated with MDA
Depressed parent encountered in PC for confirmation of depression with Hopkins Symptom Checklist-25 (HSCL25) scale. If confirmed, the adolescent will also be encountered by the GP for a screening test of depression (Adolescent Depression Rating Scale - ADRS). If negative, the patient will go out of the study. If positive, 2 others tests will be performed to study the intensity of the depression (Child depressionInventory - CDI) and the quality of life (Pediatric Quality of Life InventoryTM).Finally, the patient will be oriented to the MDA of Brest and will meet again the GP at 6 and 12 month to answers the same tests.
MDA
Depressed adolescents of depressed parents will be oriented to the MDA of Brest for depression cares.
Routine cares
Depressed parent encountered in PC for confirmation of depression with Hopkins Symptom Checklist-25 (HSCL25) scale. If confirmed, the adolescent will also be encountered by the GP for a screening test of depression (Adolescent Depression Rating Scale - ADRS). If negative, the patient will go out of the study. If positive, 2 others tests will be performed to study the intensity of the depression (Child depressionInventory - CDI) and the quality of life (Pediatric Quality of Life InventoryTM). Finally, the patient will be oriented to the routine cares and will meet again the GP at 6 and 12 month to answers the same tests.
Routine Cares
Depressed adolescents of depressed parents will be oriented to routine cares for depression cares.
Parental depression
Parental depression will be studied. Depressed adolescent encountered in MDA of Marseille for confirmation of depression with 3 tests : ADRS, CDI and PedsQL. If positive, the parent will come to the MDA for a screening test of depression (HSCL25). Parents and adolescent are seen only once.
Parental depression
Parents of depressed adolescents will be met for a screening test of depression.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
MDA
Depressed adolescents of depressed parents will be oriented to the MDA of Brest for depression cares.
Routine Cares
Depressed adolescents of depressed parents will be oriented to routine cares for depression cares.
Parental depression
Parents of depressed adolescents will be met for a screening test of depression.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Major patient consulting his GP
* Depressed patient
* Parent of adolescent aged between 11 and 18 years old
* Adolescents of groups 1 and 2 :
* Aged more than 11 and less than 18 years old
* Parent included in the study
* Parents of group 3 :
* Parent of depressed adolescent under care at the MDA of Marseille, included in the study and whose depression is confirmed by HSCL25 scale
* Adolescents of group 3 :
* Aged more than 11 and less than 18 years old
* Depressed patient
* Under care at the MDA of Marseille since less than 1 month
Exclusion Criteria
* Minor patient
* Enable to give his consent
* Patient with guardianship or curatorship
* Non consenting patient
* Pregnant or nursing mother
* Adolescents of groups 1 and 2 :
* Aged \< 11 or ≥18
* Parent whose depression isn't confirmed by HSCL25 scale
* Non consenting adolescent
* Pregnant or nursing mother
* Adolescent of group 3 :
* Aged \< 11 or ≥18
* Non depressed adolescent
* Non consenting patient
* Pregnant or nursing mother
11 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University Hospital, Brest
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Dr Phan
Brest, , France
Dr Volant-Le-Berre
Brest, , France
Dr Wauters
Brest, , France
Dr AUGUSTIN
Guilers, , France
Dr Le Grignou
Guissény, , France
Dr Ac'h
Landerneau, , France
Dr PITMAN
Landivisiau, , France
Dr CHIRON
Le Relecq-Kerhuon, , France
Dr CONNAN
Le Relecq-Kerhuon, , France
Dr Cazuguel
Locmaria-Plouzané, , France
Dr Coat-Gourio
Plougastel-Daoulas, , France
Dr NABBE
Plounéour-Trez, , France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
29BRC18.0221
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.