IMPACT: Improving Maternal Postpartum Access to Care Through Telemedicine
Recruiting
N/A
Interventional Study
Postpartum Complication
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 3,500 (estimated)
- Sponsor
- University of Texas Southwestern Medical Center · Other
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About This Trial
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.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 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…
Contacts