Care After Pregnancy Study (CAPS): Engaging Women in Postpartum Care

NCT04257552 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 128

Last updated 2022-10-21

Study results available
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Summary

The overarching hypothesis of our research agenda is that an intervention that engages economically disadvantaged women in personalized postpartum care will promote equality in maternal child health. As a first step to test our hypothesis the investigators propose the following aims:

Specific Aim 1: Measure the impact of Healthy Beyond Pregnancy on key components of postpartum care, including use of effective contraception at three and six months postpartum and breastfeeding duration at three and six months.

Specific Aim 2: Determine if Healthy Beyond Pregnancy improves adherence to health screening and linkage to follow-up care for women with cardio-metabolic complications of pregnancy.

Conditions

  • Postpartum Care

Interventions

BEHAVIORAL

Healthy Beyond Pregnancy

Web-based application grounded in tenants of behavioral economics.

BEHAVIORAL

Pre-Scheduled Postpartum Visit

Participants will have their postpartum visit scheduled while they are still in the hospital after delivery.

OTHER

Attention Control

Participants will receive texts related to infant care to mirror the attention participants receive in the Healthy Beyond Pregnancy intervention.

Sponsors & Collaborators

  • National Institute of Nursing Research (NINR)

    collaborator NIH
  • University of Pittsburgh

    lead OTHER

Principal Investigators

  • Francesca Facco, MD · University of Pittsburgh

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
12 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-02-03
Primary Completion
2021-06-02
Completion
2021-09-02

Countries

  • United States

Study Locations

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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 NCT04257552 on ClinicalTrials.gov