Screening for PTSD in Pregnant Black Women
Comparing Two Screening Approaches for PTSD to Improve Health Outcomes in Pregnant Black Women
This study tests which method works better to screen for PTSD in Black pregnant women and improve their health during pregnancy.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 804 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Emory University Academic / other |
| Locations | 2 sites (Atlanta, Georgia and 1 other locations) |
| Trial ID | NCT06522022 on ClinicalTrials.gov |
What this trial studies
This study compares two active screening interventions aimed at improving PTSD symptoms and maternal health outcomes in Black pregnant women. Researchers will evaluate the effectiveness of Culturally Responsive Screening, Brief Intervention, and Referral to Treatment (SBIRT) for obstetrics against a standard brief screening for PTSD. The study will involve Black pregnant women in their first trimester attending prenatal care visits, utilizing surveys and chart abstraction for data collection over approximately 12 months. The goal is to identify the best screening method for PTSD in this population.
Who should consider this trial
Good fit: Ideal candidates are Black pregnant women in their first trimester who have experienced at least one traumatic event.
Not a fit: Patients with active suicidality will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved mental health support and better maternal and birth outcomes for Black pregnant women experiencing PTSD.
How similar studies have performed: Other studies have shown success with culturally tailored interventions for mental health, suggesting potential effectiveness for this approach.
Eligibility criteria
Show full inclusion / exclusion 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
Where this trial is running
Atlanta, Georgia and 1 other locations
- Grady Health System — Atlanta, Georgia, United States (Recruiting)
- Truman Medical Center (TMC) system — Kansas City, Missouri, United States (Recruiting)
Study contacts
- Principal investigator: Abigail Lott, PhD, ABPP — Emory University
- Study coordinator: Abigail Powers Lott, PhD, ABPP
- Email: abigail.lott@emoryhealthcare.org
- Phone: 404-712-0159
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.