RECRUITING

Remote Postpartum Blood Pressure Monitoring and Cardiovascular Education

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

The goal of this clinical trial is to learn if patient education and regular text reminders are a feasible intervention to engage patients and reduce post partum hypertension. The main questions it aims to answer are: Is a structured postpartum remote blood pressure monitoring intervention with education and individualized medication initiation/adjustment follow-up by televisit feasible? Does a structured program reduce the occurrence of postpartum hypertension, ED visits, hospital readmissions, and adverse outcomes? Participants will: View an educational video on HDP post-delivery Receive 1-2 times daily text messages for 6 weeks postpartum Have their blood pressure medications adjusted to lower targets post partum

Official Title

Remote Postpartum Blood Pressure Monitoring and Cardiovascular Education to Reduce Emergency Department Visits, Re-admissions and Adverse Cardiovascular Outcomes in Hypertensive Disorder of Pregnancy

Quick Facts

Study Start:2025-03-17
Study Completion:2026-10-16
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06920563

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
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Age of at least 18 years.
  2. 2. Postpartum status.
  3. 3. Experience new-onset hypertension during pregnancy.
  4. 4. Enrollment in Connected MOM.
  5. 5. Ability to provide informed consent.
  6. 6. Establish medical care within the Ochsner System to facilitate data collection.
  1. 1. History of preeclampsia or gestational hypertension during previous pregnancy
  2. 2. History of chronic hypertension
  3. 3. History of coronary artery disease (myocardial infarction, coronary stent placement, coronary artery bypass grafting, spontaneous coronary artery dissection)
  4. 4. History of ischemic CVA
  5. 5. History of Congestive heart failure
  6. 6. Renal dysfunction
  7. 7. Liver dysfunction
  8. 8. Left ventricular dysfunction
  9. 9. Congenital heart disease
  10. 10. Still birth at delivery

Contacts and Locations

Study Contact

Salima Qamruddin, MD
CONTACT
+1 (504) 842-4135
salima.qamruddin@ochsner.org

Study Locations (Sites)

Ochsner Baptist
New Orleans, Louisiana, 70115
United States

Collaborators and Investigators

Sponsor: Ochsner Health System

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 Date2025-03-17
Study Completion Date2026-10-16

Study Record Updates

Study Start Date2025-03-17
Study Completion Date2026-10-16

Terms related to this study

Additional Relevant MeSH Terms

  • Pre-Eclampsia; Complicating Pregnancy
  • Gestational Hypertension