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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05795764
Other study ID # NMCSD.2022.0058
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 21, 2023
Est. completion date December 31, 2027

Study information

Verified date June 2023
Source United States Naval Medical Center, San Diego
Contact Kristen H Walter, PhD
Phone 619-540-4108
Email kristen.h.walter.civ@health.mil
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study is a randomized trial comparing outcomes of active duty service members who present to the emergency department at risk for suicide and receive care from providers trained in crisis response planning versus those providing treatment as usual.


Recruitment information / eligibility

Status Recruiting
Enrollment 700
Est. completion date December 31, 2027
Est. primary completion date September 30, 2027
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Active duty service members - >18 years old - Present to the emergency department at NMCSD with a primary concern related to suicidal ideation, plan, intention, or attempt, or are assessed as being at elevated risk of suicidal behavior - Able to understand and speak English - Able to provide consent Exclusion Criteria: - Unable to provide informed consent due to impaired mental status (e.g., acute intoxication, psychosis, mania, altered consciousness)

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Crisis Response Planning
Crisis Response Planning (CRP) is a brief psychotherapeutic intervention.
Treatment as Usual
Standard care provided for patients at risk for suicide

Locations

Country Name City State
United States Naval Medical Center San Diego San Diego California

Sponsors (3)

Lead Sponsor Collaborator
United States Naval Medical Center, San Diego Naval Health Research Center, Ohio State University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Self-Injurious Thoughts and Behaviors Interview (SITBI-R) Assessment of suicide attempts Through study completion, an average of 1 year
Primary Scale for Suicidal Ideation (SSI) Assessment of suicidal ideation; 19 items rated on a scale 0-2, higher scores indicate greater suicidal ideation severity Through study completion, an average of 1 year
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