About this trial
The mains objectives of our project are to coordinate the monitoring of suicides and to identify common or specific suicide risk factors in four overseas DROM-COM (French Polynesia, La Reunion, French Guiana and Martinique) by comparing to a site in mainland France (Amiens). A mixed approach (quantitative and qualitative) will be used, based on semi-directed interviews of the psychological autopsy type.
Eligibility criteria
Qualifiers
Persons close of the deceased
Persons who knew about his/her childhood
Age 18 or over
Interviewed for the study between 2 and 11 months after the suicide
Disqualifiers
People with neuropsychiatric disorders that may affect the quality of the information collected, cognitive (memory and expression) and judgmental functions
People who refuses to participate
Persons referred to articles L.1121-6, L.1121-7, L. 1121-8 L.1121-1-2 of the French Public Health Code.
Trial design
Treatments tested in this trial
- other
Treatment groups
Sponsors and collaborators
University Hospital Center of Martinique
Lead sponsor
Department for Research, Studies, Evaluation and Statistics, French Health and Social Affairs Ministry, France
Collaborator
French National Institute for Health and Medical Research, MOODS Unit
Collaborator
Clinical research and Innovation Office, Martinique
Collaborator
SOS KRIZ, Martinique
Collaborator
Amiens University Hospital, France
Collaborator
Suicide Prevention Resource Center, French Guiana
Collaborator
Cayenne Hospital Center, French Guiana
Collaborator
University Hospital, La Réunion
Collaborator
Tahiti Hospital Center, French Polynesia
Collaborator
Regional Health Agency, Martinique
Collaborator
Regional Health Agency, French Guiana
Collaborator
Regional Health Agency, La Somme
Collaborator
Regional Health Agency, La Réunion
Collaborator