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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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8 February 2021 |
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Main ID: |
NCT03427190 |
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Date of registration:
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30/01/2017 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Suicide Prevention Algorithm in the French Overseas Territories
APSOM |
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Scientific title:
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Assessment of Preventive Efficacy of an Algorithm Taking Place After Suicide Attempts Among Attempters Admitted to Hospital in the French Overseas Territories |
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Date of first enrolment:
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October 9, 2017 |
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Target sample size:
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259 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03427190 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Prevention. Masking: None (Open Label).
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Phase:
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N/A
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Countries of recruitment
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French Guiana
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Guadeloupe
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Martinique
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Réunion
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Contacts
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Name:
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JEHEL Louis, MD-PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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CHU de Martinique |
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Key inclusion & exclusion criteria
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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
Age minimum:
16 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Suicide Attempt
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Intervention(s)
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Other: APSOM vs Control
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Primary Outcome(s)
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Existence of a suicide
[Time Frame: 13 months]
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Existence of a suicide
[Time Frame: 6 months]
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Secondary Outcome(s)
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Assessment of suicidal risk by the Sad Persons Scale and the Columbia Suicide Severity Rating Scale (C-SSRS).
[Time Frame: 6 and 13 months after hospital discharge]
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Number of suicide attempts
[Time Frame: 6 and 13 months after hospital discharge]
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Scores at the Hospital Anxiety and Depression Scale (HADS)
[Time Frame: 6 and 13 months after hospital discharge]
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Number of deaths by suicide
[Time Frame: 6 and 13 months after hospital discharge]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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