Actively Recruiting
Randomized Controlled Trial of Two Mobile Health Strategies to Manage Postpartum Hypertension
Led by Jennifer Lewey, MD, MPH · Updated on 2026-04-22
770
Participants Needed
3
Research Sites
191 weeks
Total Duration
On this page
Sponsors
J
Jennifer Lewey, MD, MPH
Lead Sponsor
P
Patient-Centered Outcomes Research Institute
Collaborating Sponsor
AI-Summary
What this Trial Is About
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
CONDITIONS
Official Title
Randomized Controlled Trial of Two Mobile Health Strategies to Manage Postpartum Hypertension
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Delivered a baby within the past 14 days
- Diagnosed with preeclampsia or gestational hypertension during pregnancy or within 14 days postpartum
- Started blood pressure medication before hospital discharge or within 14 days after delivery
- Able to speak and understand English or Spanish
- Has phone texting capabilities
You will not qualify if you...
- Diagnosed with chronic hypertension before pregnancy
- Has pre-existing cardiovascular disease (such as prior heart attack, stroke, heart failure, ventricular tachycardia, cardiac arrest, pacemaker, severe valve disease, or prior heart surgery)
- Has chronic kidney disease stage 3 or higher
- Using three or more blood pressure medications at enrollment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
NYU Langone Health
New York, New York, United States, 10022
Not Yet Recruiting
2
The Ohio State University
Columbus, Ohio, United States, 43210
Not Yet Recruiting
3
University of Pennsylvania
Philadelphia, Pennsylvania, United States, 19104
Actively Recruiting
Research Team
J
Jennifer Lewey, MD, MPH
CONTACT
A
Alexis Giron, M.S
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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