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Recruiting NCT05766475
In-person vs. Virtual Delivery of a Group-based Prevention of Postpartum Depression
Trial Parameters
Condition Postpartum Depression
Sponsor University of Denver
Study Type INTERVENTIONAL
Phase N/A
Enrollment 900
Sex FEMALE
Min Age 18 Years
Max Age N/A
Start Date 2023-03-13
Completion 2027-06
Interventions
ROSE Program: In PersonROSE Program: Virtual
Brief Summary
The goal of this clinical trial is to test whether an established preventive intervention (group interpersonal therapy) delivered virtually shows the same benefits for preventing postpartum depression as it does when delivered in person.
Eligibility Criteria
Inclusion Criteria: * English or Spanish speaking * Less than 30 gestational weeks Exclusion Criteria: * None