RECRUITING

Use of a Cloud-connected Remote Blood Pressure Monitoring Program During the Postpartum Period for Hypertensive Women

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Hypertensive disorders (HD), including preeclampsia, gestational hypertension, chronic hypertension, and chronic hypertension with superimposed preeclampsia, affect around 10-20% of pregnant women in the United States and are significantly associated with maternal mortality and morbidity, particularly in the postpartum period. The prevalence of HD is on the rise in the United States and has increased from 13% in 2017 to 16% in 2019 owing to an increase in advanced maternal age, obesity, and diabetes. There are major racial disparities in HD and subsequent maternal mortality and morbidity. HD affect more than 1 in 5 delivery hospitalizations of Black women. Black women with HD are also more likely than white women with HD to have more adverse postpartum blood pressure trajectories which leads to a higher incidence of hypertension related hospital readmissions (readmission for hypertension during the first 6-weeks postpartum: 16.9% among Black women vs. 9.5% among white women, p=0.02) and cardiovascular-related adverse events. However, most of the management recommendations have been centered around blood pressure targets during the antepartum period with significantly less attention paid to the postpartum period despite evidence showing that hypertensive disorders are the most common reason for postpartum readmissions and are associated with increased maternal mortality and morbidity and a significant cost burden.

Official Title

Use of a Cloud-connected Remote Blood Pressure Monitoring Program During the Postpartum Period for Hypertensive Women

Quick Facts

Study Start:2024-02-13
Study Completion:2026-02
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06096701

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 54 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Pregnant individuals with hypertensive disorders
  2. * Speak English
  3. * At least 18 years old
  4. * Medicaid coverage
  5. * Between 20 weeks of pregnancy and 2 weeks postpartum
  6. * Postpartum admission at Prisma Health Richland with hypertensive disorder within 2 weeks postpartum
  1. * Not planning to deliver at Prisma Health Richland
  2. * Less than 20 weeks of pregnancy
  3. * More than 2 weeks postpartum

Contacts and Locations

Study Contact

Research nurse
CONTACT
803-687-9974
Gwendoline.Helin-milgrom@PrismaHealth.org

Study Locations (Sites)

Prisma Health Richland
Columbia, South Carolina, 29203
United States

Collaborators and Investigators

Sponsor: University of South Carolina

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-02-13
Study Completion Date2026-02

Study Record Updates

Study Start Date2024-02-13
Study Completion Date2026-02

Terms related to this study

Keywords Provided by Researchers

  • Preeclampsia
  • Gestational hypertension
  • Eclampsia
  • Chronic hypertension

Additional Relevant MeSH Terms

  • Hypertensive Disorder