In-person vs. Virtual Delivery of a Group-based Prevention of Postpartum Depression
Recruiting · NCT05766475 · Interventional (participants receive a specific treatment) · Lead sponsor: University of Denver
View the official record on ClinicalTrials.gov →Interventions studied
ROSE Program: In PersonROSE Program: Virtual
What this trial is about
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.
Who can take part
Age range
18 Years and older
Sex
Female
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- English or Spanish speaking
- Less than 30 gestational weeks
Exclusion criteria
- None
Where it is running
1 location listed across 1 US state.
- Denver Health Medical Center - Denver, Colorado, United States