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Neural Mechanisms and Predictors of an Ultra-Brief Suicide Prevention Strategy
Sponsor: Ohio State University
Summary
The current study is a clinical trial, meaning a research study in which human subjects are prospectively assigned to one or more interventions to evaluate the effects of those interventions on health-related behavioral outcomes. Specifically, male and female adults with current suicidal intent will be randomly assigned to receive either a 1-hour session of crisis response planning (CRP) or a 1-hour session of standard crisis risk management (Treatment as Usual). The effects of both conditions on changes in emotion regulation, behavioral inhibition, stress reactivity, and suicide risk will be evaluated post-intervention and at six-month follow-up. Additional assessments of changes in mood and suicidality will be collected daily during the first 10-days following intervention, and then monthly for a duration of six months. A cohort of healthy controls is included in the study but are not randomized to either treatment condition. The investigators hypothesize the following: 1) A single session of CRP will acutely change suicide risk and 2) Individuals who receive CRP will show sustained improvements in measures of suicidality when compared to individuals who received the Treatment as Usual intervention.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
191
Start Date
2021-07-28
Completion Date
2026-04-01
Last Updated
2026-02-05
Healthy Volunteers
Yes
Conditions
Interventions
Crisis Response Planning
Individuals complete an experimental collaborative suicide intervention.
Crisis Risk Counseling
Individuals complete a standard crisis risk management intervention.
Locations (1)
Ohio State University
Columbus, Ohio, United States