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NCT07209254NARecruiting

Randomized Controlled Trial of Two Mobile Health Strategies to Manage Postpartum Hypertension

Jennifer Lewey, MD, MPH

Start Date

3/2/2026

Completion Date

11/1/2029

Summary

A multicenter randomized trial that will compare the effectiveness of two postpartum blood pressure (BP) management strategies in improving blood pressure and cardiac function and increasing patient engagement and feeling of control over one's health

Eligibility Criteria

Age Range: 18 years to No maximum

Inclusion Criteria: * Age ≥18 years * Delivery within 14 days * Diagnosis of preeclampsia or gestational hypertension with or without severe features during pregnancy or within 14 days postpartum * Initiation of blood pressure medication prior to hospital discharge and up to 14 days postpartum * English or Spanish speaking (able to read/understand consent and instructions) * Has phone texting capabilities Exclusion Criteria: * Diagnosis of chronic hypertension prior to delivery (would therefore include super imposed preeclampsia) * Pre-existing cardiovascular disease (including prior myocardial infarction, stroke, heart failure with reduced ejection fraction, ventricular tachycardia, prior cardiac arrest, pacemaker, severe valvular heart disease, or prior cardiac surgery) * Chronic kidney disease (stage 3 or higher) * Using ≥3 BP medications at time of enrollment

Interventions

OTHER

High-touch blood pressure management

OTHER

Low-touch blood pressure management

Interested in This Trial?

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Conditions

Hypertension, Pregnancy Induced

Locations

NYU Langone Health

New York, New York 10022

United States

The Ohio State University

Columbus, Ohio 43210

United States

University of Pennsylvania

Philadelphia, Pennsylvania 19104

United States