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Improving Health Outcomes and Equity by Targeting Postpartum Mothers at Highest Risk — HOME  

Postpartum Depression Clinical Trial

Official title:
Improving Health Outcomes and Equity by Targeting Postpartum Mothers at Highest Risk: a Pilot Randomized Control Trial

Clinical Trial Summary

The goal of this educational clinical trial is to identify Black women most at risk for poor outcomes following delivery, the problems they experience, and to create a system to improve quality of postpartum care for high-risk women. The main question[s] it aims to answer are: - How can the investigators help postpartum Black people who have poor outcomes by decreasing the number of ED visits/readmissions for postpartum people within the first 30 days postpartum? - How can the investigators increase the ability of participants to "obtain needed services" and ability for patients to see their provider when they need to, in the 30-day post discharge period as one of the main pathways of unnecessary ED visits? Participants will be put into the study group or control group. The study group will receive a pamphlet postpartum with helpful information as well as a patient navigator who the participants will be able to reach out to their first 30 days postpartum.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06276647
Study type Interventional
Source University of Pennsylvania
Contact Micki Burdick, PhD
Phone 716-432-2558
Email micki.burdick@pennmedicine.upenn.edu
Status Recruiting
Phase N/A
Start date February 20, 2024
Completion date May 31, 2025
View Details
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