Randomized Controlled Trial of Two Mobile Health Strategies to Manage Postpartum Hypertension
Sponsored by Jennifer Lewey, MD, MPH
About this 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
Where this study is enrolling (3)
- I'm interested
NYU Langone Health
New York, New York
- I'm interested
The Ohio State University
Columbus, Ohio
- I'm interested
University of Pennsylvania
Philadelphia, Pennsylvania
Who can participate
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
Only the research team can confirm whether you qualify. The intake questionnaire is the best way to find out.
Completing a questionnaire on Clinably does not enroll you in a clinical trial or confirm your eligibility. Only the research team can determine whether you qualify to participate. These results are based on the information you provide and are intended to help you start a conversation with the research team.
Trial data sourced from ClinicalTrials.gov.