Comparing in-person and virtual group therapy to prevent postpartum depression

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial aims to evaluate the effectiveness of a group interpersonal therapy program, known as ROSE, in preventing postpartum depression (PPD) when delivered virtually versus in-person. The study focuses on pregnant women, particularly from socioeconomically disadvantaged and minoritized backgrounds, to address significant health disparities. Participants will be randomly assigned to receive the ROSE program either in-person at their prenatal care hospital or virtually through video conferencing, with sessions available in both English and Spanish. The trial will involve 900 diverse pregnant individuals to assess the scalability and accessibility of the intervention.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* English or Spanish speaking
* Less than 30 gestational weeks

Exclusion Criteria:

* None

Where it's running

• Denver Health Medical Center
  Denver, Colorado, United States Recruiting

Study contacts

• Principal investigator: Galena Rhoades, PhD — University of Denver
• Study coordinator: Galena Rhoades, PhD
• Email: Galena.Rhoades@du.edu
• Phone: 303-871-4280

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.