Feasibility and Acceptability of an Educational Intervention to Improve the Management of Depression in Primary Care.
2 other identifiers
interventional
50
1 country
1
Brief Summary
Qualitative study based on interviews and questionnaires with patients participating to an educational intervention to improve the management of depression in primary care. Objective is to assess feasibility and acceptability of an educational intervention to improve the management of depression in primary care To elaborate an educational program for the management of depression in primary care.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Nov 2010
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 2010
CompletedFirst Submitted
Initial submission to the registry
January 26, 2011
CompletedFirst Posted
Study publicly available on registry
January 27, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2014
CompletedApril 21, 2015
April 1, 2015
3.6 years
January 26, 2011
April 20, 2015
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Qualitative study
It is a qualitative study based on interviews and questionnaires with patients participating to an educational intervention to improve the management of depression in primary care.
12 months
Study Arms (1)
experimental arm
EXPERIMENTALInterventions
To elaborate an educational program for the management of depression in primary care
Eligibility Criteria
You may qualify if:
- age between 18-65y
- moderate depression (CIM 10)
- first or second episode
- able to read and understand French language
You may not qualify if:
- psychotic symptoms
- severe depression
- bipolar disorder
- suicide risk
- substance abuse
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Assistance Publique - Hopitaux de Marseille
Marseille, France
Study Officials
- PRINCIPAL INVESTIGATOR
Christophe Lancon, Professor
APHM
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 26, 2011
First Posted
January 27, 2011
Study Start
November 1, 2010
Primary Completion
June 1, 2014
Study Completion
June 1, 2014
Last Updated
April 21, 2015
Record last verified: 2015-04