Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05751473

Reducing Posttraumatic Stress Disorder (PTSD) Symptoms in First Responders and Frontline Health Care Workers

Led by University of Michigan · Updated on 2025-07-02

410

Participants Needed

12

Research Sites

171 weeks

Total Duration

On this page

Sponsors

U

University of Michigan

Lead Sponsor

N

National Institute of Mental Health (NIMH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study addresses PTSD symptoms in First Responders and Healthcare workers. Specifically, it tests whether a brief PTSD treatment (talk therapy) effectively treats PTSD when provided to First Responders and Healthcare workers by counselors in Employee Assistance Programs (EAPs). The central hypothesis is that the PTSD treatment, Prolonged Exposure for Primary Care (PE-PC), will reduce PTSD symptoms and improve functioning, compared to EAP Treatment as Usual (TAU).

CONDITIONS

Official Title

Reducing Posttraumatic Stress Disorder (PTSD) Symptoms in First Responders and Frontline Health Care Workers

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Employed at an organization served by a participating Employee Assistance Program (EAP)
  • Have a Post-Traumatic Stress Disorder Checklist for DSM-5 (PCL-5) score of 33 or higher
  • Stable psychotropic medication use for at least 4 weeks
  • For qualitative study: enrolled in the trial and identified as treatment responder or non-responder
Not Eligible

You will not qualify if you...

  • Severe cognitive impairment that likely prevents adherence to the study regimen
  • High suicide risk as defined by study criteria
  • Need for detoxification
  • Active psychosis or unmanaged bipolar disorder
  • Currently engaged in trauma-focused behavioral treatment (e.g., Prolonged Exposure or Cognitive Processing Therapy)
  • Do not speak English

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 12 locations

1

Sharp Healthcare

San Diego, California, United States, 92129

Withdrawn

2

Tanner Health System

Carrollton, Georgia, United States, 30117

Actively Recruiting

3

University of Michigan

Ann Arbor, Michigan, United States, 48109

Actively Recruiting

4

Henry Ford Health System

Detroit, Michigan, United States, 48202

Active, Not Recruiting

5

Detroit Fire Department

Detroit, Michigan, United States, 48226

Actively Recruiting

6

Health Management Systems of America

Detroit, Michigan, United States, 48226

Actively Recruiting

7

Michigan State University

East Lansing, Michigan, United States, 48824-1037

Actively Recruiting

8

West Bloomfield Fire Department

West Bloomfield, Michigan, United States, 48322

Active, Not Recruiting

9

Cope NewYork-Presbyterian

New York, New York, United States, 10017

Actively Recruiting

10

University of Cincinati Health

Cincinnati, Ohio, United States, 45229

Not Yet Recruiting

11

ProMedica

Fremont, Ohio, United States, 43420

Actively Recruiting

12

Houston Fire Department

Houston, Texas, United States, 77002

Actively Recruiting

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Research Team

J

James Garlick

CONTACT

N

Naomi Hemphill

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Reducing Posttraumatic Stress Disorder (PTSD) Symptoms in First Responders and Frontline Health Care Workers | DecenTrialz