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Recruiting Not applicable NCT07209254

Randomized Controlled Trial of Two Mobile Health Strategies to Manage Postpartum Hypertension

No applicable phase (e.g. observational)
Conditions: Hypertension, Pregnancy Induced

Sponsor: Jennifer Lewey, MD, MPH

trial.available_in: БГ
Overview
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
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
Interventions
High-touch blood pressure management
OTHER
Low-touch blood pressure management
OTHER
Locations 3
United States (3)
The Ohio State University
Columbus , Ohio
NOT_YET_RECRUITING
Anna Bartholomew, MPH, BSN, RN
NYU Langone Health
New York , New York
NOT_YET_RECRUITING
University of Pennsylvania
Philadelphia , Pennsylvania
Technical details
Status
Recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Female only
Minimum age
18 Years
Healthy volunteers
No
Start date
02.03.2026
Completion date
01.11.2029
Registry ID
NCT07209254
Source
clinicaltrials.gov
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