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NCT07060144 · ClinicalTrials.gov registry record · NA

Cognitive Processing Therapy (CPT) for Perinatal Posttraumatic Stress Disorder (PTSD)

A NA study of Pregnancy and Posttraumatic Stress Disorder (PTSD), sponsored by University of Texas at Austin.

Recruiting
Registry status
NA
Development phase
60
Enrollment target
1
Study location

NCT07060144: Recruiting NA study of Pregnancy and Posttraumatic Stress Disorder (PTSD), sponsored by University of Texas at Austin.

NCT07060144 is a NA study of Pregnancy and Posttraumatic Stress Disorder (PTSD) that is actively recruiting participants, run by University of Texas at Austin. The registered enrollment target is 60 participants, below the 872-participant average among 191 other Pregnancy trials with a reported enrollment target (93% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07060144, a NA study of Pregnancy and Posttraumatic Stress Disorder (PTSD), is actively recruiting participants, sponsored by University of Texas at Austin.

RECRUITING
Registry status
NA
Development phase
60 participants
Enrollment target
1
Study location

Study 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.

Primary Outcome

PTSD Checklist for DSM-5 (PCL-5) will be used to collect information on PTSD symptoms. The PCL-5 for DSM-5 is a 20-item self-report measure. Higher scores reflect greater PTSD severity. Scoring is based on how much the patient has been bothered by the symptoms on a scale from "0 = not at all" to "4 = extremely." PCL-5 total symptom severity scores range from 0 to 80 with higher scores indicating greater PTSD severity. PCL-5 Monthly will be collected at Visit 1, and the PCL-5 weekly will be colle

Conditions Studied

Pregnancy Posttraumatic Stress Disorder (PTSD)

Interventions

  • BEHAVIORAL Regular CPT
  • BEHAVIORAL Massed CPT

Study Locations (1)

Texas

  • University of Texas at Austin, Dell Medical School, Department of Psychiatry - Austin

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2025-07
Est. Completion 2026-12
Phase NA
University of Texas at Austin

257 total trials

What NCT07060144 shows while recruiting

NCT07060144 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 872-participant average among 191 other Pregnancy trials with a reported enrollment target (93% lower).

The record links to 2 conditions, with Pregnancy appearing as the primary indexed condition, and to 2 interventions - of which Regular CPT is the first listed.

NCT07060144 reports a single indexed study location in Texas.

Frequently Asked Questions

What is clinical trial NCT07060144 about?

NCT07060144 is a clinical study titled "Cognitive Processing Therapy (CPT) for Perinatal Posttraumatic Stress Disorder (PTSD)". 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-mi...

What is the current status of trial NCT07060144?

This trial is currently recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2025-07. Estimated completion is 2026-12.

What conditions does trial NCT07060144 study?

This clinical trial studies the following conditions: Pregnancy, Posttraumatic Stress Disorder (PTSD).

What interventions are being tested in trial NCT07060144?

The interventions under investigation include: Regular CPT (BEHAVIORAL), Massed CPT (BEHAVIORAL).

Who is sponsoring clinical trial NCT07060144?

This trial is sponsored by University of Texas at Austin, which has 257 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07060144 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Learn More About Clinical Trials

Similar trials for Pregnancy

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT07060144's enrollment target sits among peer trials

60 144th of 191 higher than 43 of 191 other Pregnancy trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Pregnancy trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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More recruiting context for NCT07060144

Source: ClinicalTrials.gov NCT07060144, the US trial registry maintained by the National Library of Medicine. NCT07060144 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.