PTSD Screening in Pregnant Black Women
Emory University · with Patient-Centered Outcomes Research Institute, University of Missouri, Kansas City · NCT06522022
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 804
- US sites recruiting
- 2
- Study start
- February 20, 2025
- Record last updated
- October 27, 2025
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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.
Being studied: Culturally Responsive SBIRT for OB; Brief Screening for PTSD
Conditions: Pregnancy Early; PTSD
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- 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.
Exclusion Criteria
- Active suicidality
Recruiting US locations
Grady Health System
Atlanta, GA 30303
Truman Medical Center (TMC) system
Kansas City, MO 64108
Site contact: Traci Johnson, MD
Study contacts (from the official record)
- Abigail Powers Lott, PhD, ABPP · 404-712-0159 · abigail.lott@emoryhealthcare.org
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