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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

TypeNameDescription
BEHAVIORALRegular CPTStandard-model Cognitive Processing Therapy (CPT) - one 60-min session per week for 12 weeks total
BEHAVIORALMassed CPTMassed 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.