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
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData 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