RecruitingNot ApplicableNCT07209254
Randomized Controlled Trial of Two Mobile Health Strategies to Manage Postpartum Hypertension
Sponsor
Jennifer Lewey, MD, MPH
Enrollment
770 participants
Start Date
Mar 2, 2026
Study Type
INTERVENTIONAL
Conditions
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
Sex: FEMALEMin Age: 18 Years
Inclusion Criteria6
- 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 Criteria4
- 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
OTHERHigh-touch blood pressure management
Twelve weeks of text-based home blood pressure monitoring with BP self-management and team-based care
OTHERLow-touch blood pressure management
10 days of text-based home blood pressure monitoring
Locations(3)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07209254
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