IMPACT: Improving Maternal Postpartum Access to Care Through Telemedicine

NCT06218355 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 3500

Last updated 2026-03-17

No results posted yet for this study

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.

Conditions

  • Postpartum Complication

Interventions

OTHER

Intensive Education

Intervention will consist of virtual education and communication through scheduled push notifications

OTHER

Enhanced Virtual Care

Intervention will utilize a telehealth model consisting of "pull" approach of patient engagement.

Sponsors & Collaborators

  • Patient-Centered Outcomes Research Institute

    collaborator OTHER
  • University of Texas Southwestern Medical Center

    lead OTHER

Principal Investigators

  • Elaine Duryea, MD · University of Texas Southwestern Medical Center

  • David B Nelson, MD · University of Texas Southwestern Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-03-01
Primary Completion
2027-09-01
Completion
2028-09-01

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06218355 on ClinicalTrials.gov