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Randomized Controlled and Prospective Trial of a Cohort of People Who Made a Suicide Attempt

Not Applicable
Completed
Conditions
Suicide, Attempted
Interventions
Other: Usual treatment and Prevention program
Other: Usual Treatment
Registration Number
NCT01176929
Lead Sponsor
Assistance Publique - Hôpitaux de Paris
Brief Summary

The prevention of recurrent suicidal about people who have made a suicide attempt is a major strand in the prevention of suicide. It is estimated that 10-15 % of people who made a suicide attempt die by suicide. Recidivism rate of suicide increases even faster than the subject is close to the index suicide attempt. A one month recurrence rate is 5 %, 12-25 % at one year. Most people who made a suicide attempt receive ambulatory monitoring. On this population, there is a low adherence to care.

The main objective of the study is to test the effectiveness of a prevention program of recurrent suicidal acts for people who made a suicide attempt.

The secondary objectives of this study are the assessment of adherence to care; the identification of sub - populations benefiting most from this program; the evaluation of the possible generalization level of the program (eligibles persons rate) and its feasibility level.

Detailed Description

This is a randomized, controlled and prospective trial comparing an experimental group (usual treatment + interventions) to a control group (usual treatment only). All participants are evaluated after one year of monitoring. The search duration is 2 years (one inclusion year and one year of follow-up). It is planned to include 330 patients, 165 patients in each group.

The program (experimental group) includes three interventions:

* A series of three telephone calls ( the second week , one month and three months after discharge from hospital )

* A systematic telephone contact with the referring physician

* A telephone helpline for people who made a suicide attempt and referring physicians.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
320
Inclusion Criteria
  • Adults ≥ 18 years.
  • Patients admitted to the emergency department for a suicide attempt.
  • Patients referred to outpatient care.
  • Patients who have given their written consent.
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Exclusion Criteria
  • Patients not affiliated to social security.
  • Patients do not have the faculties needed to be evaluated (cognitive or delusional disorder).
  • Patients hospitalized for longer than 72 hours.
  • Patients can not be recalled by phone (no phone, homeless, incarcerated)
  • Patients who do not speak French.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Interventional groupUsual treatment and Prevention programUsual treatment + prevention program of recurrent suicidal acts
Control groupUsual TreatmentUsual treatment
Primary Outcome Measures
NameTimeMethod
suicidal act frequency12 months

The primary endpoint is the occurrence of a suicidal act (occurrence or not). The suicidal act includes suicide and suicide attempt.

Secondary Outcome Measures
NameTimeMethod
suicide attempts frequency12 months

Number of occurrence of suicide attempts.

Adherence to health care12 months

Adherence to health care:

Defined by:

* The Initialization of outpatient care proposed by the suicidology's team at the initial interview or during telephone contacts.

* The number of consultations within 3 months after the first appointment with the referring doctor.

Number of eligibles persons12 months

Number of eligibles persons:

Number of people (among all people admitted to the emergency department fo a suicide attempt) meeting the criteria of selection.

Number of participants responding to telephone calls12 months

Number of participants responding to telephone calls:

We consider the failure to call after three unsuccessful telephone calls to three different days.

Number of people lost sight of12 months

Number of people lost sight of:

A person is considered lost sight if no information can be obtained after contact with the person himself, a third (nearest designated), a doctor (general practitioner and / or psychiatrist) and the nearest emergency department.

Trial Locations

Locations (1)

Assistance Publique - Hôpitaux de Paris : BICETRE Hospital

🇫🇷

Le Kremlin Bicetre, France

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