Prevention of Suicidal Behaviour With Telemedicine Techniques

Osakidetza

Status: Completed

Conditions: Suicide, Attempted

Treatments: Behavioral: Treatment as usual; Behavioral: Telephone follow up

Study type: Interventional

Funder types: Other

Identifiers

NCT03043040

2017AG01

Details and patient eligibility

About

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.

Full 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.

Enrollment: 651 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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.

Trial design

Primary purpose: Prevention

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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651 participants in 2 patient groups

Telephone follow up

Experimental group

Description:

Patients discharged from hospital A and B after a suicide attempt receive a protocolized telephone follow which is added to their usual treatment (TAU). Calls are made by nurses at weeks 1,2,4,12 and 24 after the index suicide attempt. TAU: Includes whatever treatment the doctor decides to offer to that patient (psychopharmacology, psychotherapy etc).

Treatment:

Behavioral: Treatment as usual

Behavioral: Telephone follow up

Control

Active Comparator group

Description:

Patients discharged from hospital C after a suicide attempt receive treatment as usual (whatever treatment the doctor decides to offer to that patient: psychopharmacology, psychotherapy etc).

Treatment:

Behavioral: Treatment as usual