Actively Recruiting
PTSD Screening in Pregnant Black Women
Led by Emory University · Updated on 2025-10-27
804
Participants Needed
2
Research Sites
210 weeks
Total Duration
On this page
Sponsors
E
Emory University
Lead Sponsor
P
Patient-Centered Outcomes Research Institute
Collaborating Sponsor
AI-Summary
What this Trial 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.
CONDITIONS
Official Title
PTSD Screening in Pregnant Black Women
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years or older
- 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
- Experienced at least one traumatic event in lifetime
You will not qualify if you...
- Active suicidality
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Grady Health System
Atlanta, Georgia, United States, 30303
Actively Recruiting
2
Truman Medical Center (TMC) system
Kansas City, Missouri, United States, 64108
Actively Recruiting
Research Team
A
Abigail Powers Lott, PhD, ABPP
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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