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Rationale and study design of a trial of mindfulness-based cognitive therapy for preventing suicidal behavior (MBCT-S) in military veterans.

Anna Kline, Megan S Chesin, Miriam Latorre, Rachael B Miller, Lauren M St Hill, Anton Shcherbakov, Arlene King, Barbara Stanley, Marc D Weiner, Alejandro Interian

Contemporary Clinical Trials September 2016 DOI: 10.1016/j.cct.2016.08.015 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Clinical protocol Randomized Peer reviewed
Sample size 164
Population Military veterans at high suicide risk receiving care in a Veterans Health Administration setting
Interventions Mindfulness-Based Cognitive Therapy for Preventing Suicide Behavior (MBCT-S) Safety Planning Intervention treatment as usual
Duration 10-week group intervention; assessments from baseline to 12 months post-baseline
Topics Meditation
Keywords Clinical trial Randomized controlled trial Suicide Veterans
Key points The paper describes a randomized trial protocol testing whether adding Mindfulness-Based Cognitive Therapy for Preventing Suicide Behavior to treatment as usual reduces suicide-related events in 164 high suicide risk veterans, with outcomes assessed over 12 months. The authors propose that this trial could enhance the quality and efficiency of VHA care and improve quality of life for veterans and their families.

Abstract

Although suicide ranks 10th as a cause of death in the United States, and 1st among active military personnel, there are surprisingly few evidence-based therapies addressing suicidality, and development of new treatments is limited. This paper describes a clinical trial testing a novel therapy for reducing suicide risk in military veterans. The intervention, Mindfulness-Based Cognitive Therapy for Preventing Suicide Behavior (MBCT-S), is a 10-week group intervention adapted from an existing treatment for depression (Mindfulness-Based Cognitive Therapy - MBCT). MBCT-S incorporates the Safety Planning Intervention, which is currently implemented throughout the Veterans Health Administration (VHA) for veterans at high suicide risk. MBCT-S is being tested in a VHA setting using an intention-to-treat, two-group randomized trial design in which 164 high suicide risk veterans are randomized to either VHA Treatment As Usual (TAU; n=82) or TAU+MBCT-S (n=82). Our primary outcome measure, suicide-related event, defined to include suicide preparatory behaviors, self-harm behavior with suicidal or indeterminate intent, suicide-related hospitalizations and Emergency Department (ED) visits, will be measured through five assessments administered by blinded assessors between baseline and 12months post-baseline. We will measure suicide attempts and suicide deaths as a secondary outcome, because of their anticipated low incidence during the study period. Secondary outcomes also include severity of suicidal ideation, hopelessness and depression. This study has the potential to significantly enhance the quality and efficiency of VHA care for veterans at suicide risk and to substantially improve the quality of life for veterans and their families.

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