Suicidal ideation in inpatients with depression Mental and Behavioural Disorders
Conditions
Interventions
After providing written informed consent, participants are randomized into one of two groups: the distraction intervention group or a supportive conversation control group. Randomization is conducted
Sponsors
University of Helsinki
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Unipolar depression with or without borderline personality disorder
Exclusion criteria
Exclusion criteria: 1. Psychosis 2. Involuntary treatment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Suicidal ideation assessed using the PPS-VAS immediately after the intervention or treatment as usual (TAU), and again the following morning | — |
Secondary
| Measure | Time frame |
|---|---|
| Depression, anxiety, and psychological pain measured using the modified PPS-VAS immediately after the intervention or treatment as usual (TAU), and again the following morning | — |
Countries
Finland
Contacts
Public ContactIlya Baryshnikov
Outcome results
None listed