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Clinical Trials/NCT03043040
NCT03043040
Completed
Not Applicable

Prevention of Suicidal Behaviour in High Risk Patients With Telemedicine Techniques

Osakidetza0 sites651 target enrollmentJuly 1, 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Suicide, Attempted
Sponsor
Osakidetza
Enrollment
651
Primary Endpoint
Percentage of participants in each group that make a second attempt
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

This is a multicenter controlled intervention study that aims to assess the efficacy of a telephone follow-up program for the prevention of suicidal behavior in adults discharged from general hospitals after a suicide attempt.

The hypothesis is that the implementation of this program is associated with reduced rates of suicide reattempts in these patients and also with delayed reattempts in them.

Detailed Description

Justification: Suicide is a global public health concern and is the leading cause of avoidable death in the Basque Country (Spain). The use of telemedicine techniques applied to high risk patients has shown to be useful in the prevention of suicide and suicidal behavior. Objectives: To assess the efficacy of a telephone follow-up program for the prevention of suicidal behavior in patients who recently attempted suicide. Design: This is a multicenter, prospective intervention study, non-randomized and with control group. Method: A sample of adults discharged from 2 general hospitals after a suicide attempt are enrolled in a telephone follow-up program which is added to their usual treatment (TAU). The program consists of 5 short calls made by nurses during 6 months. The calls are intended to: 1) Assess the risk of suicide in that moment, 2) Improve patient's adherence to treatments, and 3) Provide general psychoeducation guidelines. The control group is composed of patients discharged from a third general hospital after a suicide attempt. These receive TAU but are not enrolled in the telephone follow-up. Evaluation: All patients are followed during 12 months. Main outcome measures include the percentage of patients that make a second attempt and the average time to reattempt. Patients sign and informed consent.

Registry
clinicaltrials.gov
Start Date
July 1, 2014
End Date
March 31, 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Osakidetza
Responsible Party
Principal Investigator
Principal Investigator

Andrea Gabilondo

Principal Investigator

Osakidetza

Eligibility Criteria

Inclusion Criteria

  • Adult patients discharged from a General Hospital after a suicide attempt and who live in the same health sector as the hospital.
  • The suicide attempt must have been made within 24 hours prior to the appointment in the Emergency Service.

Exclusion Criteria

  • Patient with severe cognitive difficulties and in general any self-injury in which the patient does not understand the meaning or potential consequences of such behavior.
  • Patients in which a regular telephone contact is not possible.
  • Patients in which the psychiatrist who evaluates the case deems inappropriate their inclusion.
  • Patients who remain hospitalized 6 months after the attempt.

Outcomes

Primary Outcomes

Percentage of participants in each group that make a second attempt

Time Frame: 0-12 months

(Included in the title)

Secondary Outcomes

  • Average number of days from the first attempt to the second, in each group(0-12 months)
  • Mean number of reattempts in each group(0-12 months)
  • Percentage of participants in each group requiring hospitalization after the suicide attempt(0-12 months)

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