Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT07327567

Crisis Response Planning in Military Personnel With Mild Traumatic Brain Injury

A Randomized Clinical Trial Utilizing Crisis Response Planning in Military Personnel With Mild Traumatic Brain Injury

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
120 (estimated)
Sponsor
The University of Texas Health Science Center at San Antonio · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The study purpose is to test the effect of Crisis Response Planning (CRP) when used as the second method of suicide prevention in military service members who are at risk for suicide due to mild traumatic brain injury (mTBI). CRP will be compared to usual treatment. The treatment will be a 30 to 60 minute session to one person at a time either in-person or using telehealth.

Detailed description

The objective of this randomized clinical trial is to evaluate the efficacy of Crisis Response Planning as a secondary suicide prevention intervention among military service members who are at elevated risk for suicide due to their history of a mild traumatic brain injury (mTBI). CRP will be compared to a general review of available crisis resources facilitated by a therapist. Specific Aims: Aim 1: Determine the effectiveness of Crisis Response Planning (CRP) versus Treatment as Usual (TAU) on impulsivity and cognitive-affective states among military personnel with a diagnosis of mTBI. Aim 2: Understand associations between impulsivity and cognitive-affective states among military personnel with a diagnosis of mTBI. Aim 3: Determine if mTBI features (e.g., loss of consciousness duration, total number of lifetime TBIs, injury type) influence treatment outcomes.

Conditions

Interventions

TypeNameDescription
BEHAVIORALCrisis Response PlanningThe CRP intervention consists of a single 30-60-minute session. The CRP intervention includes a narrative assessment of the participant's most recent emotional crisis experience in order to understand and facilitate the participants understanding of their suicide mode.

Timeline

Start date
2026-12-01
Primary completion
2027-03-01
Completion
2027-08-01
First posted
2026-01-08
Last updated
2026-01-08

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07327567. Inclusion in this directory is not an endorsement.