← Back to Clinical Trials
Recruiting NCT06218355

IMPACT: Improving Maternal Postpartum Access to Care Through Telemedicine

Trial Parameters

Condition Postpartum Complication
Sponsor University of Texas Southwestern Medical Center
Study Type INTERVENTIONAL
Phase N/A
Enrollment 3,500
Sex FEMALE
Min Age 18 Years
Max Age N/A
Start Date 2024-03-01
Completion 2027-09-01
Interventions
Intensive EducationEnhanced Virtual Care

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 morbidity and mortality.

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 of age and older will be considered for inclusion if informed consent can be obtained. Exclusion Criteria: * 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.

Related Trials