Actively Recruiting
IMPACT: Improving Maternal Postpartum Access to Care Through Telemedicine
Led by University of Texas Southwestern Medical Center · Updated on 2026-03-17
3500
Participants Needed
2
Research Sites
235 weeks
Total Duration
On this page
Sponsors
U
University of Texas Southwestern Medical Center
Lead Sponsor
P
Patient-Centered Outcomes Research Institute
Collaborating Sponsor
AI-Summary
What this Trial Is About
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 morbidity and mortality.
CONDITIONS
Official Title
IMPACT: Improving Maternal Postpartum Access to Care Through Telemedicine
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Postpartum women who deliver a live born infant at Parkland Hospital or Grady Health and receive postpartum care at dedicated community clinics.
- Women aged 18 years and older who can provide informed consent.
- Participants must be postpartum women of reproductive age.
You will not qualify if you...
- Women who did not deliver at Parkland Hospital or Grady Health and do not receive postpartum care in the specified community clinics.
- Patients whose primary language is not English or Spanish.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Emory University School of Medicine
Atlanta, Georgia, United States, 30322
Not Yet Recruiting
2
University of Texas Southwestern Medical Center
Dallas, Texas, United States, 75390
Actively Recruiting
Research Team
J
Jacqueline Catchings, PhD
CONTACT
L
Lisa Moseley, RN
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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