Can a short talk therapy tame PTSD in those who save lives?
NCT ID NCT05751473
First seen Jul 01, 2026 · Last updated Jul 02, 2026 · Updated 1 time
Summary
This study tests whether a brief form of talk therapy, called Prolonged Exposure for Primary Care (PE-PC), can reduce PTSD symptoms in first responders and frontline healthcare workers. Participants receive 4-6 weekly 30-minute sessions either by telehealth or in person, delivered by counselors in employee assistance programs. The goal is to see if this condensed therapy works better than the usual care offered through these workplace programs.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Prolonged Exposure for Primary Care (PE-PC) talk therapy
- What this could lead to
- If effective, this brief therapy could provide a practical, accessible way to reduce PTSD symptoms in first responders and healthcare workers through workplace programs.
- What could go wrong
- This is a relatively small trial testing a condensed therapy format, and results may not apply to all workers or settings. The therapy may not work for everyone, and some participants may need more intensive treatment.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 410 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2023
- Expected to finish
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Jul 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Are employees at an orginization served by a participating EAP * Have a Post-Traumatic Stress Disorder Checklist for Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (PCL-5) score ≥33 * Have had psychotropic medication stability for at least 4 weeks Inclusion criteria for the qualitative portion of the study: \- Enrolled into the randomized clinical trial and were a treatment responder or were a treatment non-responder Exclusion Criteria: * Severe cognitive impairment that in the judgment of the investigators makes it unlikely that the participant can adhere to the study regimen (as evidenced by confusion, inability to track discussion or answer questions, or other clear and significant indicators of cognitive impairment) * High risk of suicide (defined as meeting criteria for Action Step 3 on the Participant Suicide Risk Screening form: found in protocol) * Need for detoxification * Active psychosis or unmanaged bipolar disorder, as measured by items 12 and 13 of the cross cutting assessment * Currently engagement in a trauma-focused behavioral treatment (such as Prolonged Exposure or Cognitive Processing Therapy). * Patients who do not speak English will be excluded for logistical reasons.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
11 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Cope NewYork-Presbyterian
RECRUITINGNew York, New York, 10017, United States
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Detroit Fire Department
RECRUITINGDetroit, Michigan, 48226, United States
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Duke University Health System
RECRUITINGDurham, North Carolina, 27705, United States
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Health Management Systems of America
RECRUITINGDetroit, Michigan, 48226, United States
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Henry Ford Health System
ACTIVE_NOT_RECRUITINGDetroit, Michigan, 48202, United States
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Houston Fire Department
RECRUITINGHouston, Texas, 77002, United States
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Michigan State University
RECRUITINGEast Lansing, Michigan, 48824-1037, United States
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ProMedica
RECRUITINGFremont, Ohio, 43420, United States
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Rutgers Health
RECRUITINGPiscataway, New Jersey, 08854, United States
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Sharp Healthcare
WITHDRAWNSan Diego, California, 92129, United States
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Tanner Health System
RECRUITINGCarrollton, Georgia, 30117, United States
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University of Cincinati Health
NOT_YET_RECRUITINGCincinnati, Ohio, 45229, United States
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University of Michigan
RECRUITINGAnn Arbor, Michigan, 48109, United States
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West Bloomfield Fire Department
ACTIVE_NOT_RECRUITINGWest Bloomfield, Michigan, 48322, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Five sessions to quiet trauma nightmares in bipolar disorder
- Can training hospital staff in Trauma-Informed care make childbirth safer?
- Scientists probe brain's reward system in mental illness
- Can a mindfulness class help veterans with concussion and PTSD?
- Can MDMA plus therapy help veterans fight both PTSD and alcohol addiction?
- Can talk therapies quiet the trauma of violence?