Post-Traumatic Stress Disorder (PTSD) Clinical Trials

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Prolonged Exposure Therapy to Treat Posttraumatic Stress Disorder in Pregnant Patients

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• Female

• \>18 years old

• Gestational age ≤ 25 weeks

• Meet current DSM-5 posttraumatic stress disorder criteria based on the Clinician Administered PTSD Scale for DSM-5

• Participants receiving psychotropic medications must be maintained on a stable dose for \>14 days prior to enrollment.

Locations
United States
Vermont
University of Vermont
RECRUITING
Burlington
Contact Information
Primary
Kelly Peck, PhD
kelly.peck@uvm.edu
802-656-9610
Time Frame
Start Date: 2026-02-05
Estimated Completion Date: 2027-07-22
Participants
Target number of participants: 30
Treatments
Experimental: Prolonged exposure therapy + incentives for therapy session attendance
Related Therapeutic Areas
Sponsors
Leads: University of Vermont

This content was sourced from clinicaltrials.gov