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Suicide Prevention Algorithm in the French Overseas Territories

Assessment of Preventive Efficacy of an Algorithm Taking Place After Suicide Attempts Among Attempters Admitted to Hospital in the French Overseas Territories

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03427190
Acronym
APSOM
Enrollment
259
Registered
2018-02-09
Start date
2017-10-09
Completion date
2020-10-16
Last updated
2021-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Suicide Attempt

Keywords

Suicide, Suicide attempted, Secondary Prevention, Relapse prevention, Case Management, Intervention Study

Brief summary

In France, suicide behaviours are a major public health concern that triggered the creation in 2013 of a National Observatory of Suicide. In continental France, the Algos protocol was found to be effective for the prevention of suicide attempts reiterations. This protocol is based on a procedure that keeps telephone and postal contacts with the suicide attempter and allows, via an algorithm, to assess the risk of suicide attempt recurrence, in order to intervene if necessary. Nevertheless, Algos does not involve primary care health practitioners, who could add a substantial additional efficacy, especially if they intervene downstream and in supplement to Algos. In addition, this kind of protocol has never been evaluated in the French overseas territories.

Detailed description

Since (1) Algos was never implemented in the French overseas departments (FOD) and does not involve primary care practitioners (PCP), (2) the additional effect of PCP involvement over and beyond Algos alone in unknown, and (3) little research on suicide behaviours has been conducted in the FOD, this proposal has the following main aim: to assess the effectiveness and the efficacy of the intervention, in supplement and downstream to Algos, of a healthcare professional, on the recurrence of suicide attempts in the FOD; the healthcare professional will be the patient's general practitioner, whenever possible.

Interventions

OTHERAPSOM vs Control

In complement to actions described in the control arm, the patient's general practitioner (GP) and the patient him/herself will be contacted within 21 days of hospital discharge in order to organize an appointment between them two; this consultation is expected to take place between day 22 and day 45 after hospital discharge. If the patient does not have a GP, a health-care professional (HCP) will be provided. .GP (or HCP) will also be contacted at 6 and 13 months.

Sponsors

Centre Hospitalier de Monteran, Guadeloupe
CollaboratorUNKNOWN
Centre Hospitalier Universitaire de la Guadeloupe
CollaboratorOTHER
Centre Hospitalier de Cayenne
CollaboratorOTHER
Centre Hospitalier de Ouest Guyanais Franck Joly
CollaboratorUNKNOWN
Centre d Accueil Psychiatrique Ouest-Centre, La Réunion
CollaboratorUNKNOWN
Centre d Accueil d Urgences Médico Psychologique, La Réunion
CollaboratorUNKNOWN
Centre d Accueil Psychiatrique Nord, La Réunion
CollaboratorUNKNOWN
Etablissement Publique de Santé Mentale de la Réunion
CollaboratorUNKNOWN
University Hospital Center of Martinique
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Man or woman over 16 years of age * Leaving the hospital within 15 days of the suicide attempt * Giving (him/herself or his/her legal representative)an oral consent to participate in the study * Having healthcare insurance * Reachable by phone, with possibility of confidential conversation, and by mail * Resident of Guadeloupe, French Guyana, Martinique, or Reunion Island * Able to understand and speak French

Exclusion criteria

* Homeless person * Disabled adult, person under judicial/court protection, legally incompetent adult * Participant unable to understand the study protocol, its risks and side effects, or declining to participate

Design outcomes

Primary

MeasureTime frameDescription
Existence of a suicide6 monthsReiteration of suicidal attempt after hospital discharge

Secondary

MeasureTime frameDescription
Number of suicide attempts6 and 13 months after hospital dischargeTo know total number of suicide
Number of deaths by suicide6 and 13 months after hospital dischargeTo know number of deaths by suicide
Scores at the Hospital Anxiety and Depression Scale (HADS)6 and 13 months after hospital dischargePass the scale HADS
Assessment of suicidal risk by the Sad Persons Scale and the Columbia Suicide Severity Rating Scale (C-SSRS).6 and 13 months after hospital dischargePass the scale Columbia

Countries

French Guiana, Guadeloupe, Martinique, Reunion

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026