Crisis Response Planning for Suicide Prevention

HT
Overseen ByHannah Tyler, PhD
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: The University of Texas Health Science Center at San Antonio
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

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.

Who Is on the Research Team?

HT

Hannah Tyler, PhD

Principal Investigator

The University of Texas Health Science Center at San Antonio

Are You a Good Fit for This Trial?

This trial is for adult male and female active duty military service members who are 18 or older, have had at least one mild traumatic brain injury (mTBI), regularly use a smartphone, and can read, write, and speak English.

Inclusion Criteria

I can read, write, and speak English.
I own and regularly use a smartphone.
I am an active duty military member over 18.
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Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive a 30-60 minute session of Crisis Response Planning (CRP) or Treatment as Usual (TAU) delivered individually in-person or via telehealth

1 session
1 visit (in-person or virtual)

Follow-up

Participants are monitored for changes in impulsivity, cognitive-affective states, and other psychological measures

3 months

What Are the Treatments Tested in This Trial?

Interventions

  • Crisis Response Planning

Trial Overview

The study tests Crisis Response Planning (CRP) as an additional suicide prevention method in military personnel with mTBI. CRP involves a personalized session lasting 30 to 60 minutes that can be conducted in-person or via telehealth.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: Arm 1: Crisis Response Planning (CRP)Experimental Treatment1 Intervention
Group II: Arm 2: Treatment as Usual (TAU)Active Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

The University of Texas Health Science Center at San Antonio

Lead Sponsor

Trials
486
Recruited
92,500+