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

Description

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.

Conditions

Postpartum Depression

Study Overview

Study Details

Study overview

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.

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

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

Condition
Postpartum Depression
Intervention / Treatment

-

Contacts and Locations

Denver

Denver Health Medical Center, Denver, Colorado, United States, 80204

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * English or Spanish speaking
  • * Less than 30 gestational weeks
  • * None

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Denver,

Galena Rhoades, PhD, PRINCIPAL_INVESTIGATOR, University of Denver

Elysia P Davis, PhD, PRINCIPAL_INVESTIGATOR, University of Denver

Study Record Dates

2027-06