Prolonged Exposure Therapy to Treat Posttraumatic Stress Disorder in Pregnant Patients
Part of paid clinical trials in Burlington, Vermont.
- Sponsor
- University of Vermont
- Study ID
- NCT06670079
- Status
- Recruiting
Conditions
- Posttraumatic Stress Disorder
- Pregnancy
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Prolonged exposure therapy + incentives for therapy session attendance — BEHAVIORALProlonged exposure therapy plus incentives for therapy session attendance
Study Details
The goal of this clinical trial is to learn if a treatment for adults with PTSD called prolonged exposure + incentives (PE+) works to treat pregnant patients. The main question it aims to answer is: Does PE+ decrease PTSD symptoms? All participants will receive PE+ to see if their PTSD symptoms at the end of the trial are less than at the beginning. Participants will: * Receive individual PE+ therapy for 1 hour weekly for 12 weeks. * Receive financial incentives for attending each PE+ session. * Attend assessment visits every 4 weeks for the 12 weeks of the trial. * Allow research staff to collect some information about their labor and delivery from their medical records after their babies are born.
Key Dates
- Start date
- Feb 5, 2026
- Status verified
- May 2026
- Primary completion
- Jul 15, 2027
- Completion
- Jul 22, 2027
Study Design
- Enrollment
- 30 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Prolonged exposure therapy + incentives for therapy session attendance
Primary Outcome Measure
Change in Posttraumatic Stress Disorder Symptom Severity - Clinician Rated [ Time Frame: From baseline to the 12-week assessment ]
Central Contacts
- Kelly Peck, PhD802-656-9610
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Vermont | Burlington | Vermont | 05401 |
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