Actively Recruiting
Real-Time Assessment of Emotion Regulation Strategies Used by Suicidal Military Personnel
Led by Ohio State University · Updated on 2026-02-19
334
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
O
Ohio State University
Lead Sponsor
M
Medical University of South Carolina
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating how Crisis Response Planning, a one-session behavioral intervention, helps reduce suicidal thoughts and behaviors among active U.S. military servicemembers. The study aims to understand which emotion regulation strategies work best in different situations and for whom, improving suicide prevention efforts. This research also explores how personal and social factors influence the effectiveness of these strategies over time. Participants will engage in a single session where they collaboratively create a personalized Crisis Response Plan that includes identifying personal suicide warning signs, self-regulation techniques, reasons for living, sources of social support, and access to professional crisis services. They will write this plan down and receive counseling to limit access to potentially lethal means. The intervention focuses on strengthening emotion regulation to reduce suicidal ideation. Throughout 28 consecutive days, participants will complete real-time assessments of their suicidal thoughts using ecological momentary assessment tools on their smartphones. Follow-up assessments using the Scale for Suicide Ideation will occur at multiple time points up to 12 months. Researchers will monitor changes in suicidal ideation and related factors, as well as mental health treatment engagement. Participants must have regular smartphone access and the ability to complete remote activities during the study.
CONDITIONS
Brief Title
Assessment of Emotion Regulation Strategies Used When Suicidal
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Currently serving in any Branch or Component of the U.S. military
- 18 years old or older
- Score 5 or higher on the Scale for Suicidal Ideation or report a suicide attempt, aborted attempt, or interrupted attempt within the past month
- Ability and willingness to complete research activities remotely
- Regular access to a compatible Android or Apple smartphone
You will not qualify if you...
- Engaged in mental health treatment or taking psychotropic medications within the past year
- Psychiatric or medical conditions preventing informed consent or participation (e.g., psychosis, mania, acute intoxication)
- Expecting to separate from the military within 90 days
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit (remote)
Duration - 1 day
Participants complete a one-session Crisis Response Planning intervention and receive lethal means safety counseling to develop personalized strategies for managing suicide risk.
1 visit (remote)
Duration - 28 consecutive days
Participants report suicidal ideation and emotion regulation strategies daily using ecological momentary assessments for 28 consecutive days after treatment.
Daily remote assessments for 28 days
Duration - 12 months
Participants complete follow-up assessments of suicide ideation at multiple time points up to 12 months to monitor ongoing outcomes.
7 remote follow-up assessments at baseline, 1, 2, 3, 6, 9, and 12 months
Trial Site Locations
Total: 1 location
1
The Ohio State University Wexner Medical Center
Columbus, Ohio, United States, 43214
Actively Recruiting
Research Team
L
Lauren Khazem, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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