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The Amager Project: Intervention After Suicide Attempt

Rigshospitalet logo

Rigshospitalet

Status

Unknown

Conditions

Suicidal Behaviour
Repetition of Suicidal Behaviour

Treatments

Behavioral: OPAC (Outreach, Problem solving, Adherence, Continuity)

Study type

Interventional

Funder types

Other

Identifiers

NCT00821756
AH-2005

Details and patient eligibility

About

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.

Enrollment

133 patients

Sex

All

Ages

12+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Suicide attempt and self harm

Exclusion criteria

  • Severe mental diagnosis (schizophrenia, psychosis, bipolar affective disorder, severe/psychotic depression, severe dementia)

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

133 participants in 2 patient groups

1
Experimental group
Description:
Assertive intervention in OPAC-style: Outreach,problem solving,adherence,continuity
Treatment:
Behavioral: OPAC (Outreach, Problem solving, Adherence, Continuity)
2
No Intervention group
Description:
Control arm: Treatment as usual

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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