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Early Intervention for Postpartum PTSD: Comparing Written Exposure and Capnometry-Guided Breathing Therapy - Phase 1

Key facts

Who runs it
Stanford University
Where
Little Rock and Palo Alto, United StatesSee the 2 sites
Trial code
Status
Recruiting
People taking part
10 people, planned
Started
9 Mar 2026
Expected to end
Mar 2027
Type of study
Interventional, 2 groups
Treatments tested
  • Written Exposure Therapy (WET)
  • Capnometry-Guided Breathing Intervention (CGRI)
Record updated
13 November 2026

Who can take part

Age
18 years and older
Sex
Women only
Healthy volunteers
Cannot take part

The registry criteria, word for word

Show all 10 criteriaShow less

Who can take part

  • Age ≥18
  • Delivered a live infant within 5 days
  • Severe maternal morbidity or infant admitted to NICU
  • PCL-5 ≥28
  • English-speaking
  • Able to consent and participate

Who cannot take part

  • Cognitive impairment preventing participation
  • Active psychosis or mania
  • Current suicidal crisis
  • Current suicidal intent or plan

Where in United States

  • University of Arkansas for Medical SciencesLittle Rock, United StatesContact: Heather MoodyTaking people
  • Stanford UniversityPalo Alto, United StatesNo longer taking part

About the trial

What the trial wants to find out

The purpose of this study is to assess the feasibility and acceptability of two early interventions, Written Exposure Therapy (WET) and Capnometry-Guided Breathing Intervention (CGRI), for reducing post-traumatic stress disorder (PTSD) symptoms following childbirth. This initial non-randomized pilot study aims to identify potential barriers and inform refinements to the interventions and study procedures for a subsequent randomized feasibility trial.

The 2 groups in the trial

  • Written Exposure Therapy (WET)Treatment being tested

    Participants will complete 5 writing sessions. One 50-minute session will be held in the hospital before discharge, followed by four 50-minute sessions by secure video once a week. Sessions are delivered by a trained study therapist under licensed clinician supervision.

  • Capnometry-Guided Breathing Intervention (CGRI)Treatment being tested

    Participants will complete one 45-minute in-hospital training session using the device, which includes a tablet and breathing sensor. They will then practice guided breathing at home twice daily for about 17 minutes each time for 4 weeks, with weekly phone check-ins from study staff.

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Early Intervention for Postpartum PTSD: Comparing Written Exposure and Capnometry Guided Breathing Therapy - Phase 1
Record updated
13 November 2026