Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID05722197

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 screening and enrollment visit (remote)

Outpatient Treatment

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)

Monitoring

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

Long-term Monitoring

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

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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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