In-person vs. Virtual Delivery of a Group-based Prevention of Postpartum Depression
Recruiting
N/A
Interventional Study
Postpartum Depression
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 900 (estimated)
- Sponsor
- University of Denver · Other
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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.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* English or Spanish speaking
* Less than 30 gestational weeks
Exclusion Criteria:
* None
Contacts