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RECRUITING
NCT05766475
NA

In-person vs. Virtual Delivery of a Group-based Prevention of Postpartum Depression

Sponsor: University of Denver

View on ClinicalTrials.gov

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.

Official title: Group-based Prevention of Postpartum Depression: In-person vs. Virtual Delivery

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

900

Start Date

2023-03-13

Completion Date

2027-06

Last Updated

2023-05-17

Healthy Volunteers

No

Interventions

BEHAVIORAL

ROSE Program: In Person

In-person preventative intervention for postpartum depression that includes content on building social support and communication skills in relationships, navigating the role transition to motherhood, and learning about signs and symptoms of depression after delivery.

BEHAVIORAL

ROSE Program: Virtual

Virtual ROSE covers the same content (e.g. improving social support and communication) and is delivered by the same facilitators as the in-person intervention via telehealth.

Locations (1)

Denver Health Medical Center

Denver, Colorado, United States