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Study identifier: NCT05751473 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: Post Traumatic Stress Disorder  ·  Sponsor: University of Michigan

PhaseNA
Planned participants410
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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).

This description comes directly from the study's public registry record.

Talk to the study team

James Garlick  ·  734-232-2663  ·  jgarlick@med.umich.edu

Always discuss trial participation with your own doctor first.

Locations (14)

Sharp HealthcareSan Diego, California, United StatesWithdrawn
Tanner Health SystemCarrollton, Georgia, United StatesRecruiting
University of MichiganAnn Arbor, Michigan, United StatesRecruiting
Henry Ford Health SystemDetroit, Michigan, United StatesActive Not Recruiting
Detroit Fire DepartmentDetroit, Michigan, United StatesRecruiting
Health Management Systems of AmericaDetroit, Michigan, United StatesRecruiting
Michigan State UniversityEast Lansing, Michigan, United StatesRecruiting
West Bloomfield Fire DepartmentWest Bloomfield, Michigan, United StatesActive Not Recruiting
Rutgers HealthPiscataway, New Jersey, United StatesRecruiting
Cope NewYork-PresbyterianNew York, New York, United StatesRecruiting
Duke University Health SystemDurham, North Carolina, United StatesRecruiting
University of Cincinati HealthCincinnati, Ohio, United StatesNot Yet Recruiting

+ 2 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05751473