- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02932709
Effect of Telephone Follow-up on Repeated Suicide Attempt in Patients (EXBRAYAT)
Effect of Telephone Follow-up on Repeated Suicide Attempt in Patients Discharged From an Emergency Psychiatry Department: a Controlled Study
Attempted suicide is a major public health problem, and the efficacies of current postvention protocols vary. The investigators evaluated the effectiveness of telephone follow-up of patients referred to an emergency psychiatric unit for attempted suicide on any further attempt/s over the following year.
In a single-center, controlled study with intent to treat, they evaluated the efficacy of a protocol of telephone follow-up of patients at 8, 30, and 60 days after they had been treated for attempted suicide. For comparison, they evaluated as controls patients with similar social and demographic characteristics referred to their emergency psychiatric unit in the year prior to the study who did not receive telephone follow-up after their initial hospitalization. Data were analyzed using logistic regression.
Study Overview
Detailed Description
The importance of suicide and suicidal attempts recurrence is a major public health problem. Indeed, the suicide attempt is one of the most important predictors of suicide, as well as suicidal relapse is considered a suicide risk factor. It is therefore essential to establish the suicidal relapse prevention devices.
Moreover, the consensus conference on suicidal crisis (6) in particular stresses the importance of organizing continuity of care and foster a therapeutic alliance to avoid a break in continuity of care.
This study aims to evaluate the effectiveness of telephone Callback patients on suicide rate of recurrence at 6 months of suicidal gesture. A secondary objective is to assess and promote compliance.
Patients were included after a psychiatric interview following a suicide attempt in the North hospital's emergency unit no emergency hospitalization or indication in the interview before the release of the psychiatric emergency service. The interview provides an assessment of suicide risk and oral information about the protocol. A map showing the coordinates of the psychiatric emergency service and a reminder of the protocol is given. A consent form is signed. This protocol does not replace the usual care.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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SAINt-ETIENNE, France, 42055
- CHU Saint-Etienne
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patient affiliated or entitled to a social security scheme
- Patient who have attempted suicide regardless of the medium
- Patient falling 4 psychiatric sectors covered by the CHU of Saint-Etienne
- Major and minor Patient (with parental permission)
- Patient for which there is no evidence of psychiatric hospitalization sector or clinic immediately after switching to the suicidal act
Exclusion Criteria:
- Homeless Patient
- Patients for whom Callback is not possible (no phone, incarceration ...)
- Patient who do not speak French
- Patient admitted sector or clinic following the psychiatric interview inclusion
- Patient Refusal
- Medical Reason
- Deleterious character of recontact by a doctor of the psychiatric emergency after passing the act
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Patients admitted of Psychiatry
Only patients who had a suicide attempt admitted to the Department of Emergency Psychiatry.
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suicide attempt : We evaluated the effectiveness of telephone follow-up of patients who had referred to an emergency psychiatric unit for attempted suicide on any further attempt/s over the following year.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Comparison of suicidal recurrence rate
Time Frame: 6 months
|
Number of relapses of suicide attempts per patient over a period of 6 months.
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assess the impact of the device on the number of deaths by suicide
Time Frame: 6 months
|
Number of deaths by suicide
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6 months
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assess the impact on adherence to treatments
Time Frame: 6 months
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The rate of adherence to treatments
|
6 months
|
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Measuring the time between the TS and the first recurrence
Time Frame: 6 months
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Time of recurrence compared to the suicide attempt
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6 months
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Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Catherine Massoubre, PhD, CHU Saint-Etienne
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1008071
- 2010-A00804-35 (Other Identifier: ANSM)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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