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In-person vs. Virtual Delivery of a Group-based Prevention of Postpartum Depression
Recruiting
Group-based Prevention of Postpartum Depression: In-person vs. Virtual Delivery
Who can join
Ages 18 and older · Women
Full eligibility criteria
Inclusion Criteria: * English or Spanish speaking * Less than 30 gestational weeks Exclusion Criteria: * None
About the study
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.
What is being tested
- ROSE Program: In Person (behavioral)
- ROSE Program: Virtual (behavioral)
Sponsor: University of Denver · Participants: 900 · Started: Mar 13, 2023
Contact the study team
- Galena Rhoades, PhD · Phone: 303-871-4280
Official record on ClinicalTrials.gov — NCT05766475
Locations in the U.S.
| Colorado | Denver Health Medical Center, Denver |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.