suicidal ideation R45.8
Conditions
Interventions
Group 1: The present study will be a randomized controlled trial with two groups. Participants will be patients with a current diagnosed psychiatric disorder. The allocation to the two groups will be
Sponsors
Medizinische Universität Wien
Eligibility
Sex/Gender
All
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Current diagnosed psychiatric disorder
Exclusion criteria
Exclusion criteria: Diagnoses F00-F09, acute risk of self-harm or harm to others; unable to provide informed consent; insufficient knowledge of German language; overall bad health condition
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Suicidal ideation based on Reasons for living inventory; measured at T1, T2, & T3 (immediately before and after the intervention; approx. one week later) | — |
Secondary
| Measure | Time frame |
|---|---|
| Data will becollected before (T1) and after article exposure (T2) as well as one week later (T3). Measured variables: - Primary outcome variable: suicidal ideation (measured with the Reasons for Living Inventory) - Secondary outcome variable: suicide-related knowledge (measured with 5 items of the Facts on Suicide Quiz), hopelessness (measured with the Beck Hopelessness Scale), mood (measured with the Affective State Scale), stigmatizing attitudes toward suicidal individuals (measured with the Short Stigma of Suicide Scale), and help-seeking behavior (measured with the General Help seeking Questionnaire). Other variables: identification with the respective protagonist in the article (measured with the Cohen Identification Scale only at T2). | — |
Countries
Austria
Contacts
Public ContactThomas Niederkrotenthaler
Medizinische Universität Wien, Zentrum für Public Health, Abteilung für Sozial- und Präventivmedizin, Unit Suizidforschung & Mental Health Promotion
Outcome results
None listed