Status:
RECRUITING
IMPACT: Improving Maternal Postpartum Access to Care Through Telemedicine
Lead Sponsor:
University of Texas Southwestern Medical Center
Collaborating Sponsors:
Patient-Centered Outcomes Research Institute
Conditions:
Postpartum Complication
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
The purpose of this study is to compare two complex, multi-component evidence-based postpartum interventions in underserved populations of lower socioeconomic status in an effort to reduce maternal mo...
Detailed Description
This large, multi-center randomized controlled trial will compare two multi-component postpartum care models via hybrid type 1 design conducted in two phases. An initial phase (phase 1) will collect b...
Eligibility Criteria
Inclusion
- Postpartum women who deliver a live born infant at Parkland Hospital or Grady Health and receive postpartum care at dedicated community clinics.
- Due to the nature of the study, all will be women, and all will be postpartum, thus of reproductive age. Postpartum women 18 years of age and older will be considered for inclusion if informed consent can be obtained.
Exclusion
- Postpartum women who do not deliver at Parkland Hospital or Grady Health will not receive postpartum care in the pre-specified community clinics for Parkland health systems.
- Patients with a primary language other than English or Spanish.
Key Trial Info
Start Date :
March 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
September 1 2028
Estimated Enrollment :
3500 Patients enrolled
Trial Details
Trial ID
NCT06218355
Start Date
March 1 2024
End Date
September 1 2028
Last Update
March 10 2025
Active Locations (2)
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1
Emory University School of Medicine
Atlanta, Georgia, United States, 30322
2
University of Texas Southwestern Medical Center
Dallas, Texas, United States, 75390