Suicide, Attempted
Conditions
Keywords
suicide, attempted, prevention, telemedicine
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.
Interventions
BEHAVIORALTelephone follow up
Already described in previous page
BEHAVIORALTreatment as usual
Already described in previous page
Sponsors
Eusko Jaurlaritza
Osakidetza
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE
Intervention model description
This is a non-randomized non-blinded multicenter intervention study with control group. Patients from hospital A and B are included in the intervention group. Patients from hospital C are included in the control group.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
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.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Percentage of participants in each group that make a second attempt | 0-12 months | (Included in the title) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Average number of days from the first attempt to the second, in each group | 0-12 months | (Included in the title) |
| Mean number of reattempts in each group | 0-12 months | (Included in the title) |
| Percentage of participants in each group requiring hospitalization after the suicide attempt | 0-12 months | (Included in the title) |
Outcome results
None listed