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Taking people in United StatesNo phase

PTSD Screening in Pregnant Black Women

Key facts

Who runs it
Emory University
Where
Atlanta and Kansas City, United StatesSee the 2 sites
Trial code
Status
Recruiting
People taking part
804 people, planned
Started
20 Feb 2025
Expected to end
Mar 2029
Type of study
Interventional, 2 groups
Treatments tested
  • Culturally Responsive SBIRT for OB
  • Brief Screening for PTSD
Record updated
27 October 2026

Who can take part

Age
18 years and older
Sex
Women and men
Healthy volunteers
Can take part

The registry criteria, word for word

Show all 8 criteriaShow less

Who can take part

  • 18+ years old,
  • Ability to provide informed consent,
  • English-speaking,
  • Willingness to participate in the study,
  • Self-identification as Black or African American,
  • Pregnant and in the first trimester attending initial prenatal care visit,
  • Endorsement of at least one traumatic event in their lifetime

Who cannot take part

  • Active suicidality

Where in United States

  • Grady Health SystemAtlanta, United StatesContact: Abigail Powers Lott, PhD, ABPPTaking people
  • Truman Medical Center (TMC) systemKansas City, United StatesContact: Traci Johnson, MD (principal investigator)Taking people

About the trial

What the trial wants to find out

This study will compare the effectiveness of two active screening interventions in improving post-traumatic stress disorder (PTSD) symptoms, maternal perinatal care utilization, satisfaction utilization of mental healthcare services, and maternal health and birth-related outcomes for Black pregnant women.

The 2 groups in the trial

  • Culturally Responsive SBIRT for OBTreatment being tested

    Participants randomized to Culturally Responsive SBIRT for OB will participate in the intervention visit (20-30 minutes) while waiting for their OB visit (or after the visit if time does not allow) and then engage in their prenatal care visit as usual. If any safety concerns emerge during the visit, the lay provider will contact the clinical staff on the study

  • Brief Screening for PTSDTreatment being tested

    Participants randomized to Brief Screening For PTSD, screening will be conducted as part of regular clinic activities during the initial prenatal care visit. Specifically, clinic staff (nurse, PA) or study staff will ask the questions in the PC-PTSD-5 along with the standard procedure to administer the Edinburgh Postnatal Depression Scale (EPDS), and the provider will review the results with the patient during the prenatal care visit and provide referral resources regardless of screen outcome. Positive PTSD screens (PC-PTSD-5 ≥ 3) will be referred to the hospital's integrated care team following the same model as positive EPDS screens.

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
Comparing Two Screening Approaches for PTSD to Improve Health Outcomes in Pregnant Black Women
Record updated
27 October 2026