In-person vs. Virtual Delivery of a Group-based Prevention of Postpartum Depression
ConditionPostpartum Depression
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorUniversity of Denver
About this trial
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 criteria
Qualifiers
English or Spanish speaking
Less than 30 gestational weeks
Disqualifiers
None
Trial design
Treatments tested in this trial
- ROSE Program: In Person
- ROSE Program: Virtual
Treatment groups
900 Participants
are divided into 2 treatment groupsSponsors and collaborators
University of Denver
Lead sponsor
National Institute of Mental Health (NIMH)
Collaborator
Denver Health Medical Center
Collaborator
Source ClinicalTrials.gov