Home › High Blood Pressure in Pregnancy › NCT07209254
Randomized Controlled Trial of Two Mobile Health Strategies to Manage Postpartum Hypertension
Recruiting
Who can join
Ages 18 and older · Women
Full eligibility criteria
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
About the study
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
What is being tested
- High-touch blood pressure management (other)
- Low-touch blood pressure management (other)
Sponsor: Jennifer Lewey, MD, MPH · Participants: 770 · Started: Mar 2, 2026
Contact the study team
- Jennifer Lewey, MD, MPH · Phone: 215-662-7700
Official record on ClinicalTrials.gov — NCT07209254
Locations in the U.S.
| New York | NYU Langone Health, New York |
| Ohio | The Ohio State University, Columbus (Not yet recruiting) |
| Pennsylvania | University of Pennsylvania, Philadelphia |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.