Resilience Training for PTSD in First Responders

(FiRST Trial)

Not yet recruiting at 1 trial location
AG
Overseen ByAdam Gonzalez
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Stony Brook University
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?

As a result of chronic exposures to traumatic and stressful events, first responders are at elevated risk for experiencing post-traumatic stress disorder (PTSD) and other mental health problems. Resilience training can reduce the risk for developing mental health symptoms in first responders. The National Institute for Environmental Health Sciences and the Substance Abuse Mental Health Services Administration developed the Worker Resilience Training (WRT) program - a 4-hour interactive workshop to educate responders on the effects of traumatic exposures, PTSD and ways to increase adaptive coping resources and promote resilience. The investigators completed a randomized clinical trial (RCT) of the WRT for active responders (n = 167). Results indicated that the WRT, as compared to a waitlist control group, helped prevent the development of PTSD and depression symptoms, and improved important resilience indicators (i.e., healthy lifestyle behaviors, stress management, physical activity) over the course of three months. The proposed multi-site RCT seeks to build on our initial study by conducting a Stage III efficacy trial of the WRT workshop in N=800 first responders in New York (NY) and Texas (TX). Our specific aims are: Aim 1. To evaluate the efficacy of the WRT program for improving resilience indicators, defined as health promoting lifestyle behaviors, stress management and physical activity, and improving perceived resilience over the course of one year. Aim 2. To evaluate whether the WRT program serves to prevent the development or worsening of psychological symptoms and impairments in functioning over the course of one year among those first responders who are exposed to traumatic events after participation in the study workshop. Aim 3. To identify the target treatment mechanisms of the WRT for preserving mental and occupational health outcomes and functioning over the course of one year in first responders who are exposed to traumatic events post-workshop. Aim 4. To gather qualitative data to further inform a future effectiveness trial including perceptions about the use and potential impact of peer leaders delivering the program content, and perceptions about mode of program delivery via open-ended questions at follow-up. The investigators will use a cluster RCT design and multi-modal assessments including self-report measures, a web-based stress reactivity performance task, and real-time accelerometry. Participants in both conditions will also receive a booster session at 3 months post workshop to reinforce skills and intervention knowledge. This study will contribute to our understanding of how resilience training may serve to protect the mental health and functioning of first responders. This study has important clinical and public health implications, including preserving/strengthening mental health and reducing overall personal and financial costs. This study also takes a research to practice approach by working collaboratively with fire departments and EMS organizations in NY and TX. If successful, the investigators will work with these leaders to develop a method for annual WRT trainings to foster resilience and promote well-being long-term for first responders.

Who Is on the Research Team?

AG

Adam Gonzalez

Principal Investigator

Stony Brook University

Are You a Good Fit for This Trial?

Inclusion Criteria

Active first responder at fire station or EMS organization

Exclusion Criteria

This criterion does not apply to me.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Workshop

Participants attend a 4-hour Worker Resilience Training (WRT) or Fire and Medical Safety (FAMS) workshop

1 day
1 visit (in-person or virtual)

Booster Session

Participants receive a booster session to reinforce skills and intervention knowledge

1 day
1 visit (in-person or virtual)

Follow-up

Participants are monitored for resilience indicators and mental health outcomes

12 months
5 visits (virtual) at 1, 3, 6, 9, and 12 months

What Are the Treatments Tested in This Trial?

Interventions

  • Worker Resilience Training Program

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: Worker Resilience Training ProgramExperimental Treatment1 Intervention
Group II: Fire and Medical Safety (FAMS)Active Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Stony Brook University

Lead Sponsor

Trials
225
Recruited
41,700+

National Institute of Mental Health (NIMH)

Collaborator

Trials
3,007
Recruited
2,852,000+

Texas A&M University

Collaborator

Trials
156
Recruited
28,900+

Feinstein Institute for Medical Research

Collaborator

Trials
22
Recruited
5,700+