Remote Postpartum Blood Pressure Monitoring and Cardiovascular Education

Recruiting now · Not applicable

Conditions studied: Pre-Eclampsia; Complicating Pregnancy, Gestational Hypertension

In brief

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

Key facts

Study ID

NCT06920563

Run by

Ochsner Health System

People needed

296

Starts

2025-03-17

Expected to finish

2026-10-16

Last updated by the study team

2025-04-09

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Age of at least 18 years.
• Postpartum status.
• Experience new-onset hypertension during pregnancy.
• Enrollment in Connected MOM.
• Ability to provide informed consent.
• Establish medical care within the Ochsner System to facilitate data collection.

You may not qualify if…

• History of preeclampsia or gestational hypertension during previous pregnancy
• History of chronic hypertension
• History of coronary artery disease (myocardial infarction, coronary stent placement, coronary artery bypass grafting, spontaneous coronary artery dissection)
• History of ischemic CVA
• History of Congestive heart failure
• Renal dysfunction
• Liver dysfunction
• Left ventricular dysfunction
• Congenital heart disease
• Still birth at delivery

Where it is running

• Ochsner Baptist — New Orleans, Louisiana, United States (enrolling)

Full record on ClinicalTrials.gov

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