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NCT Number: NCT05773898

Contribution of Psychological Autopsy to the Understanding of Suicidal Behaviors in French Overseas Territories

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Centre Hospitalier Universitaire de Martinique - Hôpital Pierre ZOBDA QUITMAN

Fort-de-France, France, 97261, Martinique

Location status: Recruiting

Location contact

SEBASTIEN CAVALINI

CONTACT

[email protected]

+596 596 592 696

About this study

Epidemiological studies on suicide are rare in Overseas France. Nevertheless, studies conducted independently in New Caledonia (NC) and French Guiana were able to highlight a high prevalence of suicides in minority indigenous populations (Kanaks and Amerindians). These data therefore suggest a socio-cultural variability of suicides within the different territories. Psychological autopsies (used in NC) are an innovative approach that has already proven worldwilde its effectiveness in researching socio-cultural factors and prevalence of mental disorders in suicide subjects (Inserm). However, the qualitative analysis of psychological autopsies, even if it is very complete, is limited to known factors of suicide risk. Given the ethnic specificities of suicidal behavior and the socio-cultural richness of each overseas territory, an exploratory anthropologic approach will make it possible to complete identification of risk factors for suicide or combinations of these specific factors (profiles).

Our project will improve the data collection of suicide cases with the implementation of a network in each site (Public Health Department, Emergency units, Coroner offices, GP, associations, families…). Then interview with proxies of subjects deceased by suicide will allow psychological autopsy (questionnaires SCID to detect mental disorders, Life Trajectories, to detect life events and their burden, Anthropologic for socio-cultural aspects and Psycholinguistic analysis).

The total duration of the project will be 24 months with the recruitment of a maximum of 30 cases per site. Duration of the inclusion period will be 23 months, duration of follow-up per participant 1 month. The follow-up interview will be carried out one month after the inclusion interview. It will make it possible to establish a post-vention of suicide among the bereaved and an evaluation of the impact of the psychological autopsy interviews and the life trajectories of the bereaved.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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.

Treatment and study plan

other

Other

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.

Primary outcomes

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

    Time frame: 1 month

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

Secondary outcomes

  1. Assessment and comparison of risk factors and mental disorders

    Time frame: 1 month

    The number of risk factors identified and the number of mental disorders detected will be compared between the overseas territories and the Somme department.

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

    Time frame: 1 month

    The variables related to childhood violence will be presented with the number of subjects "n" expressed as a percentage.

  3. Score of adversity by the Life Trajectory Questionnaire

    Time frame: 6 month

    Once the interviews have been completed, the recordings will be transcribed semi-automatically via the HappyScribe® online platform. The resulting verbatim recordings will then be used as data for psycholinguistic and anthropological analyses.

    The qualitative data will then be transformed into quantitative data following the methodology developed by Brown and Harris, in which a panel of experts (researchers from our team and clinicians) assigns an overall rating for each five-year period, according to the severity of the burden of adversity carried by the person. This rating, from 1 to 6, makes it possible to determine the burden of adversity in the development of the individual (detailed description Séguin et al, 2007). It is the ratings of adversity that will form the curve of these trajectories.

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

    Time frame: 6 month

    an audio-recording will record responses to semi-structured interview using anthropological approach. After transcription, the qualitative data gained from these questions will be analyzed using thematic analysis to understand the main themes (Representations of mental illness and suicidal commitment. Religious beliefs and cultural practices. Use of traditional methods to treat mental illness).

    A part of the transcription will also be analyzed using psycholinguistic approach. The words will be defined according to their frequency of occurrence and the most frequent grouped according to several "reference universes" associated with central notions (e.g. feeling, sensation, behavior, time, family, crisis, suicide, etc.). The visualization of the reference universes will summarize the frequency and proximity of key words and will make it possible to obtain a cognitive and mental representation of the speech.

Study contacts

Contact information is provided by the study sponsor or research team.

SEBASTIEN CAVALINI

CONTACT

[email protected]

+596 596 592 696

VERONIQUE ERDUAL

CONTACT

[email protected]

+596 596 553 554

Sponsors and collaborators

Lead sponsor

University Hospital Center of Martinique

Other

Collaborators

  • Amiens University Hospital, France
  • Cayenne Hospital Center, French Guiana
  • Clinical research and Innovation Office, Martinique
  • Department for Research, Studies, Evaluation and Statistics, French Health and Social Affairs Ministry, France
  • French National Institute for Health and Medical Research, MOODS Unit
  • Regional Health Agency, French Guiana
  • Regional Health Agency, La Réunion
  • Regional Health Agency, La Somme
  • Regional Health Agency, Martinique
  • SOS KRIZ, Martinique
  • Suicide Prevention Resource Center, French Guiana
  • Tahiti Hospital Center, French Polynesia
  • University Hospital, La Réunion

Registry information

Acronym: AUTOPSOM

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Mar 17, 2023
Registry last updated
Sep 26, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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