No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
804 (estimated)
Sponsor
Emory University · Other
Who this trial is looking for
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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.
Trial Locations
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State
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Status
Eligibility 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 t…
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
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