Actively Recruiting

Age: 18Years +
FEMALE
Healthy Volunteers
ID06741436

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

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Enrollment and Baseline Assessment

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)

Postpartum Monitoring and Follow-up Assessments

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

Loading map...

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

"Smart Family Doctor" Assisted Comprehensive Management of S...

Post Coronary Artery Bypass Grafting

Actively Recruiting

1 location

The PILI 'Aina Project to Improve Cardiometabolic Health in...

Type 2 Diabetes

Actively Recruiting

2 locations

Vascular Function in Health and Disease: Rehabilitation for ...

Chronic Obstructive Pulmonary Disease

Actively Recruiting

1 location

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