Trials / Recruiting
RecruitingNCT07060144
Cognitive Processing Therapy (CPT) for Perinatal Posttraumatic Stress Disorder (PTSD)
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- Sponsor
- University of Texas at Austin · Academic / Other
- Sex
- Female
- Age
- 18 Years – 46 Years
- Healthy volunteers
- Not accepted
Summary
Pregnant women with a primary diagnosis of posttraumatic stress disorder (PTSD) (PTSD Checklist for DSM-5 (PCL-5) score \> 33) will be randomized to receive conventional cognitive processing therapy (CPT) (60-min session once/week for 12 weeks) or massed CPT (mCPT) (an intensive schedule of 12 60-min sessions over 5 days, approximately 2-3 sessions per day) via telemedicine, for treatment of PTSD. The research aims will be three-fold: (1) Evaluate the relative efficacy and tolerability of CPT vs. mCPT for treatment of perinatal PTSD and depression; (2) Determine the effect of CPT upon maternal-infant attachment and interaction; (3) Collect pilot data of obstetric and neonatal outcomes among those receiving the two CPT delivery schedules.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BEHAVIORAL | Regular CPT | Standard-model Cognitive Processing Therapy (CPT) - one 60-min session per week for 12 weeks total |
| BEHAVIORAL | Massed CPT | Massed CPT - two 60-min sessions each day for 5 consecutive days (10 sessions total) |
Timeline
- Start date
- 2025-07-01
- Primary completion
- 2026-12-01
- Completion
- 2026-12-01
- First posted
- 2025-07-11
- Last updated
- 2025-07-11
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT07060144. Inclusion in this directory is not an endorsement.