PTSD Screening in Pregnant Black Women
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorEmory University
About this trial
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.
Eligibility criteria
Qualifiers
18+ years old,
Ability to provide informed consent,
English-speaking,
Willingness to participate in the study,
Disqualifiers
Active suicidality
Trial design
Treatments tested in this trial
- Culturally Responsive SBIRT for OB
- Brief Screening for PTSD
Treatment groups
804 Participants
are divided into 2 treatment groupsSponsors and collaborators
Emory University
Lead sponsor
Patient-Centered Outcomes Research Institute
Collaborator
University of Missouri, Kansas City
Collaborator
Source ClinicalTrials.gov