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NCT06920563NARecruiting

Remote Postpartum Blood Pressure Monitoring and Cardiovascular Education

Ochsner Health System

Start Date

3/17/2025

Completion Date

10/16/2026

Summary

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

Eligibility Criteria

Age Range: 18 years to No maximum

Inclusion Criteria: 1. Age of at least 18 years. 2. Postpartum status. 3. Experience new-onset hypertension during pregnancy. 4. Enrollment in Connected MOM. 5. Ability to provide informed consent. 6. Establish medical care within the Ochsner System to facilitate data collection. Exclusion Criteria: 1. History of preeclampsia or gestational hypertension during previous pregnancy 2. History of chronic hypertension 3. History of coronary artery disease (myocardial infarction, coronary stent placement, coronary artery bypass grafting, spontaneous coronary artery dissection) 4. History of ischemic CVA 5. History of Congestive heart failure 6. Renal dysfunction 7. Liver dysfunction 8. Left ventricular dysfunction 9. Congenital heart disease 10. Still birth at delivery

Interventions

OTHER

Video

OTHER

Text Reminder

OTHER

Blood pressure threshold

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Conditions

Pre-Eclampsia; Complicating PregnancyGestational Hypertension

Locations

Ochsner Baptist

New Orleans, Louisiana 70115

United States