NCT07209254Recruiting
Randomized Controlled Trial of Two Mobile Health Strategies to Manage Postpartum Hypertension
Source: ClinicalTrials.gov · Last updated 22 May 2026
Brief summary (registry, in English)
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
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 770 (estimated)
- First submitted
- 30 Sept 2025
- Start date
- Mar 2026
- Primary completion date
- Oct 2029
- Lead sponsor
- Jennifer Lewey, MD, MPH
- Diseases
- High blood pressure
- NCT number
- NCT07209254
What you commit to
- Study type: Interventional
- Planned participants: 770
- From Mar 2026 to the primary completion date, Oct 2029
- 3 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Diagnosis of chronic hypertension prior to delivery (would therefore include super imposed preeclampsia)
- Using ≥3 BP medications at time of enrollment
Other illness
- Chronic kidney disease (stage 3 or higher)
Lab values
- 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)
Who the study is looking for
- 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
Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers
Sites (3)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| The Ohio State University Coordinator of this site? Confirm its status | Columbus | United States | Not yet recruiting |
| NYU Langone Health Coordinator of this site? Confirm its status | New York | United States | Recruiting |
| University of Pennsylvania Coordinator of this site? Confirm its status | Philadelphia | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.