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The goal of this clinical trial is to evaluate whether enhanced brief cognitive behavioral therapy (E-BCBT) can help reduce suicidal thoughts and behaviors among psychiatric inpatients. This therapy is designed to be feasible during hospitalization and includes self-directed worksheets that may later be used independently after discharge, offering potential benefits for suicide prevention outside the hospital setting as well.
Participants will be randomly assigned to one of two groups:
All participants will take part in five assessments: one before treatment, one after treatment, and three monthly follow-up assessments over the three months after discharge. Assessments include interviews, conducted in person or by phone, and questionnaires, completed online via a survey link. The entire study period will take approximately four months.
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Inclusion criteria
Participants must meet all of the following criteria to be eligible for the study:
Hospitalized following a suicide crisis
*A suicide crisis is defined based on the Columbia-Suicide Severity Rating Scale (C-SSRS) as meeting at least one of the following: A. A suicide attempt within 1 week prior to admission B. Current suicidal ideation and plan at the time of admission (recorded as the reason for hospitalization) and at least one prior suicide attempt within the past 2 years
Aged 18 years or older
Diagnosed with a depressive disorder or bipolar and related disorder based on the Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM-5) using the Mini International Neuropsychiatric Interview (M.I.N.I.) at screening
Able to read and write in Korean without difficulty
Capable of understanding the study procedures and providing written informed consent voluntarily
Exclusion criteria
Participants will be excluded if any of the following apply:
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30 participants in 2 patient groups
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Central trial contact
Eunbyeol Lee, Ph.D.; Christopher Hyung Keun Park, M.D., Ph.D.
Data sourced from clinicaltrials.gov
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