Psychoeducational Course for Suicide Prevention

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-99
SponsorSt. Olavs Hospital

About this trial

The plan is to include patients with a history of increased risk of suicide. In the aftermath of an episode of imminent suicide risk, patients will receive a psychoeducational course that entails information on different aspects of suicide-related topics, identifying triggers and detecting early warning signals for increased suicide risk. The course culminates in working on completing a individual safety plan to prevent an future increase in suicide risk. The course will incorporate both patients and their next of kin. The psychoeducational course will be compared to a control group where the patients receive one individual session with focus on a safety plan to evaluate the intervention. Both groups will receive treatment as usual (TAU) during both the acute phase and follow-up. The study will be conducted as a randomized controlled trial.

Eligibility criteria

Qualifiers

Patients with a suicide attempt, suicidal behavior, or risk of suicidal behavior and a clinician evaluating that the patient has an intention to die

Patients with a suicide attempt or suicidal behavior defined as "a self-inflicted, potentially injurious behavior with a non-fatal outcome for which there is evidence of intention of death and/or considered to have had or been close to a suicidal crisis syndrome.

Disqualifiers

Not being sufficiently fluent in Norwegian to provide informed consent, valid responses on psychometric testing or to benefit from a psychoeducative course.

A known diagnosis of ICD-10 F 60.3 (borderline personality disorder) with similar symptoms at previous admittances.

Ongoing psychosis.

A substance abuse condition to such a degree that they are unable to comply with the protocol and are considered to be at risk when attending psychoeducational courses.

Trial design

Treatments tested in this trial

  • Psychoeducational Course for Suicide Prevention
  • Individual therapy session
  • Treatment as usual

Treatment groups

80 Participants
are divided into 2 treatment groups

Sponsors and collaborators

St. Olavs Hospital

Lead sponsor

Helse Nord-Trøndelag HF

Collaborator

Norwegian University of Science and Technology

Collaborator