Randomized Controlled Trial of Two Mobile Health Strategies to Manage Postpartum Hypertension
Sponsor: Jennifer Lewey, MD, MPH
Trial Details
| Condition | Hypertension, Pregnancy Induced |
| Intervention | High-touch blood pressure management; Low-touch blood pressure management |
| Phase | NA |
| Status | Recruiting |
| Participants | 770 |
| Est. Completion | 1 Oct 2029 |
| Last Updated | 22 May 2026 |
Primary Outcome
Mean diastolic blood pressure (DBP)
Eligibility Criteria
Inclusion 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
Trial Sites
Countries
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