RecruitingNot ApplicableNCT05766475

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

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

Sponsor

University of Denver

Enrollment

900 participants

Start Date

Mar 13, 2023

Study Type

INTERVENTIONAL

Conditions

Postpartum Depression

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

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is comparing two formats — in-person and virtual — of a group program designed to prevent postpartum depression in pregnant women. Researchers want to know which format is more effective and accessible. **You may be eligible if...** - You are currently pregnant at fewer than 30 weeks of gestation - You speak English or Spanish **You may NOT be eligible if...** - There are currently no other exclusion criteria listed for this study Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALROSE 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.

BEHAVIORALROSE 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.