Actively Recruiting
Identification of Early Heart Failure With Preserved Ejection Fraction After Preeclampsia by Exercise Stress Testing
Led by Vanderbilt University Medical Center · Updated on 2026-04-14
500
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Cardiovascular disease (CVD) is the leading cause of death among women, but research has often focused on older women after cardiometabolic risks have accumulated. This study explores pregnancy as an early time of cardiovascular stress that may reveal a woman's risk for CVD, particularly looking at preeclampsia (PreE). Researchers aim to understand if PreE contributes directly to heart dysfunction later in life and to identify early signs of heart failure with preserved ejection fraction (HFpEF) linked to PreE. Participants include women diagnosed with PreE and a control group without PreE or pre-existing diabetes or chronic hypertension. The study involves recruiting women in their third trimester or upon admission to labor and delivery services. Researchers will collect data through surveys, blood pressure monitoring at home, blood tests, and specialized heart function tests including brachial artery reactivity testing and echocardiography at several time points: shortly after delivery, 12-16 weeks postpartum, and about one year postpartum. Exercise stress testing and leg lift maneuvers will assess heart function under stress. Participants will be monitored through blood pressure checks up to twice daily at home, with readings recorded electronically or manually. Heart imaging and exercise tests will measure heart function at rest and during stress. Blood and urine samples will be collected to study vascular and inflammatory markers related to PreE. The main outcome is to relate postpartum heart function changes to pregnancy-specific risk factors in women with and without PreE. Participants' health and safety will be closely followed throughout the study, which may last up to one year after delivery.
CONDITIONS
Brief Title
Exercise Testing After Preeclampsia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women age greater than 18 years
- Give birth at Vanderbilt University Medical Center
- Have a diagnosis of preeclampsia based on American College of Obstetricians and Gynecologists criteria
- Controls must meet the same inclusion/exclusion criteria except no preeclampsia, no pre-existing diabetes, and no chronic hypertension
You will not qualify if you...
- Age less than 18 years
- Unable to provide informed consent
- Does not speak English
- Active COVID-19 infection
- Residual symptoms from prior COVID-19 infection
- HIV infection
- Hepatitis B or C infection
- Pulmonary arterial hypertension
- Sickle cell disease
- Pulmonary embolism
- Pre-existing cardiomyopathy
- Coronary artery disease
- Active substance abuse (except tobacco or marijuana)
- Unable to attend postpartum visits
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Within 48 hours of delivery
Participants provide informed consent and complete baseline surveys and questionnaires. Initial cardiovascular assessments including vital signs, rest echocardiography, and biomarker collection occur within approximately 48 hours of delivery. Participants receive an at-home blood pressure monitor with instructions for use.
1 visit (in-person)
Duration - Up to 1 year postpartum
Participants self-monitor blood pressure up to twice daily using provided monitors. Follow-up visits at approximately 12-16 weeks postpartum and approximately 1 year postpartum include surveys, cardiovascular assessments (vital signs, rest and perturbational echocardiography with exercise testing, brachial artery reactivity testing), and biomarker collection. Urine samples are also collected at follow-up visits.
2 visits (in-person) at approximately 12-16 weeks and 1 year postpartum; daily at-home blood pressure monitoring between visits
Trial Site Locations
Total: 1 location
1
Vanderbilt University Medical Center
Nashville, Tennessee, United States, 37203
Actively Recruiting
Research Team
O
Olivia H Patridge, BS
C
Cassandra F Reynolds, BS, CCRC
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here