Clinical trial Recruiting at 2 sites Interventional Ages 18 and up

PTSD treatment delivered by your primary care nurse

Official title: A Hybrid Implementation-Effectiveness Trial of Nurse-Delivered Post-Traumatic Stress Disorder Treatment in Primary Care

Run by Rush University Medical Center · NCT07430657 · Data updated 2026-11-12

This will test whether nurses trained to deliver a short, four-session trauma therapy can help primary care patients who develop PTSD after a recent life-threatening heart or stroke event.

More Post-traumatic Stress Disorder (PTSD) trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment100 (estimated)
SponsorRush University Medical Center
Academic / other
Locations2 sites (Chicago, Illinois and 1 other locations)
StatusRecruiting
StartedMarch 30, 2026
Main results expectedJune 2028
Study endsSeptember 2029
Registry record updatedApril 29, 2026
Trial IDNCT07430657 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are Rush primary care patients with PTSD symptoms (PCL-5 ≥28 and endorsed trauma) following a life-threatening cardiovascular event within the past 90 days.

Probably not a fit

Patients with acute safety risks (for example active suicidal ideation), those already receiving psychotherapy for PTSD, or those lacking decisional capacity are excluded and unlikely to benefit from this program.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This Type 2 hybrid implementation-effectiveness trial will enroll about 100 primary care patients who develop PTSD symptoms after a life-threatening cardiovascular event. Participants at Rush University Medical Center sites are randomized to NurseNET—a manualized, nurse-delivered four-session Narrative Exposure Therapy integrated into primary care—or to usual referral to PTSD treatment. The trial measures PTSD symptoms, functional outcomes, and implementation metrics such as feasibility and acceptability of nurse delivery. Safety procedures include screening out participants with acute safety risks or current PTSD psychotherapy and monitoring capacity to consent.

Why it matters

Potential benefit: If successful, NurseNET could expand access to effective, brief PTSD therapy by letting trained primary care nurses provide treatment close to where patients already receive care.

How similar studies have gone: Narrative Exposure Therapy has evidence as an effective trauma intervention and other task-shifting models where nurses deliver mental health care have shown promise, but nurse-delivered NET in primary care for recent cardiovascular event survivors is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* o PTSD + trauma exposure (PCL-5 score ≥28, plus trauma endorsed on LEC-5/CAPS)

  * Life-threatening CV event in the last 90 days (including myocardial infarction/heart attack, acute cerebrovascular accident/stroke, sudden cardiac arrest, acute decompensated heart failure, or life-threatening arrhythmia requiring cardioversion or defibrillation).
  * Primary care patient at Rush University Medical Center

Exclusion Criteria:

* o Safety risk (documented suicidal ideation/need for acute psychiatric care)

  * NET conflict (actively receiving psychotherapy/PTSD treatment)
  * Cognitive/decisional non-capacity (University of California, San Diego Brief Assessment of Capacity to Consent \[UBACC\] ≤ 14.5)

Where it's running

  • Rush University Medical Center
    Chicago, Illinois, United States
    Recruiting
  • Rush University Medical Center
    Brookfield, Wisconsin, United States
    Recruiting

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.