Crisis Response Planning for Military Personnel

Suicidal Ideation Clinical Trial

— ASPIS/CRP  

Official title:

Moderators of the Effectiveness of Crisis Response Planning (CRP) for Military Personnel

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05795764
• Other study ID #: NMCSD.2022.0058
• Status: Recruiting
• Phase: N/A
• 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
• 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)

Related Conditions & MeSH terms

• Suicidal
• Suicidal Ideation
• Suicide
• Suicide Threat

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