Status:
NOT_YET_RECRUITING
Randomized Controlled Trial of Two Mobile Health Strategies to Manage Postpartum Hypertension
Lead Sponsor:
Jennifer Lewey, MD, MPH
Collaborating Sponsors:
Patient-Centered Outcomes Research Institute
Conditions:
Hypertension, Pregnancy Induced
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief 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 e...
Eligibility Criteria
Inclusion
- 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
- 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
Key Trial Info
Start Date :
December 1 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
November 1 2029
Estimated Enrollment :
770 Patients enrolled
Trial Details
Trial ID
NCT07209254
Start Date
December 1 2025
End Date
November 1 2029
Last Update
October 6 2025
Active Locations (3)
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1
New York University
New York, New York, United States, 10022
2
The Ohio State University
Columbus, Ohio, United States, 43210
3
University of Pennsylvania
Philadelphia, Pennsylvania, United States, 19104