NCT05773898

Brief Summary

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.

Trial Health

57
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
150

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jan 2024

Geographic Reach
1 country

1 active site

Status
recruiting

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

First Submitted

Initial submission to the registry

March 7, 2023

Completed
10 days until next milestone

First Posted

Study publicly available on registry

March 17, 2023

Completed
10 months until next milestone

Study Start

First participant enrolled

January 25, 2024

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2025

Completed
Last Updated

September 26, 2024

Status Verified

September 1, 2024

Enrollment Period

1 year

First QC Date

March 7, 2023

Last Update Submit

September 24, 2024

Conditions

Keywords

SuicidePsychological autopsiesepidemiologyrisk factorspsycholinguistic approachFrench overseas territories

Outcome Measures

Primary Outcomes (1)

  • Existence of risk factors and mental disorders evaluated by Structured Clinical Interview for Diagnostic (SCID)

    Number and percentage of mental disorders presented by the deceased and identified on the basis of data collected during DSM 5 diagnostic interviews.

    1 month

Secondary Outcomes (4)

  • Assessment and comparison of risk factors and mental disorders

    1 month

  • Existence or not of violence in childhood or during life among suicide cases

    1 month

  • Score of adversity by the Life Trajectory Questionnaire

    6 month

  • Existence of language, social and anthropological elements associated with suicide risk factors

    6 month

Study Arms (1)

person close to the deceased

Relatives will be invited to participate in two semi-structured research interviews in the form of a storytelling interview with an interviewer. All interviews will be conducted after obtaining the participants' non-objection. The interviews will be recorded and, once transcribed, will be analysed.

Other: other

Interventions

otherOTHER

The interviewers will collect data from relatives using questionnaires and evaluation grids based on an identification form, a Life Trajectory questionnaire, an anthropological evaluation grid, a retrospective psychiatric diagnosis questionnaire (SCID), a socio-demographic questionnaire, a questionnaire on suicide risks and a questionnaire on emotional state.

person close to the deceased

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study population corresponds to the relatives of a person who died by suicide. The deceased had been living for at least two years in one of the five study territories and information on cause of death information was obtained from potential sources on suicide victims.

You may qualify if:

  • 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

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre Hospitalier Universitaire de Martinique - Hôpital Pierre ZOBDA QUITMAN

Fort-de-France, France, 97261, Martinique

RECRUITING

Related Publications (1)

  • Amiot M, Amadeo S, Merle S, Guidere M, Jehel L, Seguin M, Spodenkiewicz M. Identifying suicidal risk factors in the French Overseas Territories with multimethod psychological autopsy (AUTOPSOM): a mixed-methods study protocol. BMJ Open. 2024 Jul 16;14(7):e079405. doi: 10.1136/bmjopen-2023-079405.

MeSH Terms

Conditions

SuicideMental Disorders

Condition Hierarchy (Ancestors)

Self-Injurious BehaviorBehavioral SymptomsBehavior

Study Officials

  • STEPHANE AMADEO, Pr

    University hospital, Martinique

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 7, 2023

First Posted

March 17, 2023

Study Start

January 25, 2024

Primary Completion

February 1, 2025

Study Completion

April 1, 2025

Last Updated

September 26, 2024

Record last verified: 2024-09

Locations