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UnknownNCT00821756

The Amager Project: Intervention After Suicide Attempt

The Amager Project. Intervention After Suicide Attempt: A Randomized Study.

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
133 (actual)
Sponsor
Rigshospitalet, Denmark · Academic / Other
Sex
All
Age
12 Years
Healthy volunteers
Not accepted

Summary

Background: Repetition rate after a suicide attempt and self harm is very high, about 12-30 percent. Studies, reviewed by Hawton, 1999 show a lack of evidence for psychosocial interventions. Compliance with aftercare is also often very poor. Objective: Inspired by the Norwegian Baerum project, the aim is to study if active, assertive outreach, seeking contact, talking about problem solution, motivate to comply to other appointments, will reduce repetition of suicidal acts in the following years. Methods: The design is a prospective randomized, controlled trial. The patients (immediately after a suicide attempt or deliberate self harm)) included are randomized to intervention or standard (treatment as usual), aiming at at least 60 persons in each arm. The intervention is carried out through research nurses with about 8 home visits, phone contact, phone messaging, e-mails.Included are persons 12 years of age and older, danish speaking without translator and without diagnoses of severe mental illness (schizophrenia, bipolar illness, mania and severe/psychotic depression) or severe dementia. Results: Outcome is measured by repetition of suicidal act (suicide attempt, self harm or completed suicide)as recorded in medical records and by the Danish Cause of Death Register. Repetition measured by persons and by acts throughout 1 year, 2 and 3 years periods. Additional outcome is number and character of health system contacts.

Conditions

Interventions

TypeNameDescription
BEHAVIORALOPAC (Outreach, Problem solving, Adherence, Continuity)Assertive outreach immediately after the suicide attempt with about 8 home visits plus contact by telephone, phone messages, e-mails. Duration of intervention 6 months.

Timeline

Start date
2005-01-01
Primary completion
2008-08-01
Completion
2010-08-01
First posted
2009-01-13
Last updated
2009-01-13

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT00821756. Inclusion in this directory is not an endorsement.