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Pregnancy Complications, CardiovascularHOPENCT06517628

The Heart Outcomes in Pregnancy Expectations for Mom and Baby Study

An observational study of Pregnancy Complications, Cardiovascular, run by University of Missouri, Kansas City at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This is a prospective, observational study which is evaluating the obstetrical, neonatal, and cardiovascular outcomes of 1000 pregnant people with known heart disease to define how best to structure cardio-obstetrics care to optimize outcomes. Read more about this study

Who is it for?
Ages 18 years and older, women only
Conditions the study is for
Pregnancy Complications, Cardiovascular
What is being tested?
Purely observational study on the care and outcomes of participants with cardiovascular disease in pregnancy.
How many people
1,000 participants
Where
1 siteUnited States
Study dates
14 Jan 2025to 30 Jun 2028
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Study population: Pregnant people with cardiovascular disease

Who may be able to join

  • Must have one or more condition(s) within the 6 following categories - Repaired or Unrepaired
  • Congenital or structural heart disease
  • Aortopathies
  • Arrhythmias
  • Cardiomyopathies and Heart Failure
  • Coronary disease
  • Other (Current endocarditis or history of endocarditis, Pericarditis, Pericardial effusion - Moderate or Large, Pericardial constriction, Pulmonary hypertension (all types) defined as mean pulmonary artery systolic pressure of >20 mmHg by right heart catheterization or pulmonary hypertension estimated in the severe range by echo)

Who cannot join

  • Unable to participate in telephone follow-up
  • Too hard of hearing to do follow-up by telephone or deaf
  • Incarcerated prisoner
  • History of dementia.
  • Subjects without a way for contact by telephone for follow-up
  • Refused participation in the study
Show all 9Show fewer
  • Unable to consent for self
  • Traumatic Aortic Disease
  • Peripartum cardiomyopathy diagnosed in current pregnancy

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Karen L Florio, DO, MPH contact

631-579-1030

klwa42@umsystem.edu

Anna Grodzinsky, MD, MS contact

816-932-2000

agrodzinsky@saint-lukes.org

United States1 site, 1 recruiting
  • Saint Luke's Hospital of Kansas City

    Kansas City, Missouri, 64111

    Rosann Gans, RN, BSN, 816-932-6122, rgans@saint-lukes.org

    Nancy Stone, MEd, 8169325367, nanstone@saint-lukes.org

    Recruiting

Other trials in United States

About this study

This is a prospective, observational study which is evaluating the obstetrical, neonatal, and cardiovascular outcomes of 1000 pregnant people with known heart disease to define how best to structure cardio-obstetrics care to optimize outcomes.

Read the detailed description

The US is the only industrialized nation to experience a rise in maternal mortality over the last decade. Despite the Healthy People 2030 agenda target of reducing maternal mortality by 10%, rates in the United States are predicted to increase. Furthermore, maternal mortality disproportionately impacts Black, Hispanic, American Indian/Alaskan Native (AIAN), and Asian/Pacific Islander birthing people, who die at a rate that far greater than their White counterparts. Black birthing people are twice as likely to experience severe maternal morbidity (SMM) and 3-4X more likely to die, even after adjusting for demographic and hospital factors. Unfortunately, this gap is widening, with a 20% increase in death for Blacks as compared with a 5% rise in Whites over the last decade. Understanding contributors to adverse outcomes for marginalized birthing populations cannot solely be determined from retrospective chart adjudication and requires prospective evaluation to better understand patient and treatment factors contributing to maternal morbidity and mortality.

Despite affecting only 2-4% of pregnancies, cardiovascular disease (CVD) accounts for >30% of maternal deaths, making it a leading cause of maternal mortality for all birthing people and the number one cause in the Black population. Pregnant people with acquired and congenital heart disease experience the majority of CV-related morbidity and mortality, of which over three quarters have been deemed preventable. The prevalence of CVD is expected to grow as risk factors for CV-related death (obesity, advanced maternal age, hypertensive disorders, and preexisting heart disease) are rising dramatically in pregnant people, which disproportionately burdens marginalized populations. Provider-based factors are a leading cause of preventable morbidity, yet the lack of evidence-based guidelines, means of risk-stratifying pregnant people with CVD, or insight into how best to structure care limits the ability to improve maternal outcomes.

Mortality is not the only important outcome for pregnant people with CVD. For every maternal death, it is estimated that 100 people - 50,000 per year - will suffer severe maternal morbidity (SMM) during delivery, with significant costs to both their families and the economy. Adverse pregnancy outcomes (APOs) and neonatal adverse clinical events (NACEs), including pre-eclampsia, preterm delivery, fetal growth restriction, stillbirth and maternal hemorrhage, are all significantly more common in those with heart disease. Pregnant people who survive these events are more likely to suffer post-traumatic stress and depression, which can adversely impact mother-child bonding and long-term health. Importantly, there are no studies in this population evaluating quality of life, which cannot be measured using retrospective data.

To address the critical need for reversing the US trend in maternal morbidity and mortality, the Heart Outcomes in Pregnancy Expectations (HOPE) study will focus on the highest risk population, pregnant people with CVD. It will provide deeper insights into maternal risk factors, their association with care, and the influence of alternative structures of cardio-obstetric care with APO, MACE, and NACE outcomes. It is a multi-site, multidisciplinary prospective study at >30 cardio-obstetrics clinics throughout the US with a key secondary goal of better understanding racial disparities in care and outcomes. Not only will traditional APOs, MACE, and NACE events from presentation to 1-year after delivery be collected, generic and disease-specific quality of life will be measured as a way to evaluate their independent impact on outcomes.

Preliminary insights through our pilot program highlight the importance of better structures of care as a means of improving outcomes, which has previously been established in other clinical settings, but not in cardio-obstetrics care. The investigators have identified 6 key structures of care that have been variably adopted through the US and for which additional data to define their independent association with outcomes is needed.

These include:

  1. multidisciplinary (OB/maternal-fetal medicine [MFM], cardiology, anesthesia, critical care, etc.) care teams;
  2. a COB care coordinator;
  3. coordinated inter-disciplinary patient evaluation;
  4. team debriefing
  5. the ability to perform high-risk deliveries in the ICU and
  6. formalized warm hand offs to primary or sub-specialty care after delivery.

After adjusting for extensive patient factors associated with adverse outcomes, the independent association of these structures of care with outcomes will be estimated as a foundation for testing and disseminating those that are most effective.

Being tested
Purely observational study on the care and outcomes of participants with cardiovascular disease in pregnancy.
Keywords
Pregnancy, cardio-obstetrics, Structures of Care, Quality of Care, Disparities, Heart disease in pregnancy, Pregnancy complications, Adverse pregnancy outcomes, Major adverse cardiac events, Neonatal adverse events, Quality of life
Medical subject headings
Pregnancy Complications, Cardiovascular, Pregnancy Complications, Cardiovascular Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Purely observational study on the care and outcomes of participants with cardiovascular disease in pregnancy.Other

    The primary exposure variable is the organization of cardio-obstetrics care which will be defined by annual site surveys and its association with outcomes will be defined by hierarchical models adjusting for patient characteristics.

Study groups in NCT06517628
Study groupRoleWhat they receive
Pregnant people with cardiovascular diseaseAny pregnant patient with acquired or congenital cardiovascular disease upon presentation to a cardio-obstetrics clinic.
Receives: Other: Purely observational study on the care and outcomes of participants with cardiovascular disease in pregnancy.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Rate of Adverse pregnancy outcomes

    HELLP, preeclampsia, gestational hypertension, eclampsia, superimposed preeclampsia on chronic hypertension (SIPE), premature preterm rupture of membranes (PPROM), preterm delivery, thrombotic complications, hemorrhage, maternal mortality, placental abruption, Admission ICU delivery

    Measured: up to 6 weeks postpartum

Secondary outcomes (2)
  1. Rate of Maternal Adverse Cardiac Events (MACE)

    A composite outcome including any of the following: cardiovascular death, non-fatal stroke, myocardial infarction, hospitalization for acute coronary syndromes, urgent revascularization procedures, decompensated heart failure, aortic dissection, clinically significant arrhythmia requiring treatment (eg. atrial fibrillation/flutter, SVT, ventricular tachycardia, etc), cardiac transplant

    Measured: Up to 1 year postpartum

  2. Rate of Neonatal adverse clinical events (NACE)

    A composite outcome including any of the following: APGARS < 8 at 5 minutes, birthweight of < 2500 grams, NICU admission, supplemental oxygen use, neonatal death, fetal death, spontaneous abortion/miscarriage, intrauterine fetal growth restriction

    Measured: Through maternal hospital discharge

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Jul 2024
  2. Study start14 Jan 2025
  3. Primary completion30 Jun 2028 (estimated)
  4. Study completion30 Jun 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
1,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06517628
Sponsor's protocol ID
0073599
Acronym
HOPE
Status last verified
Jan 2025
First submitted
8 Jul 2024
Last updated
20 Jan 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Data will be deposited into BioLincc (https://biolincc.nhlbi.nih.gov/). These data will be provided in a completely de-identified format with random shifting of dates that are internally consistent with the participant's actual experiences.

Questions about this trial

What is this clinical trial studying?

An observational study of Pregnancy Complications, Cardiovascular, run by University of Missouri, Kansas City at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 20 Jan 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Karen L Florio, DO, MPH (631-579-1030, klwa42@umsystem.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Rate of Adverse pregnancy outcomes (time frame: up to 6 weeks postpartum). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Jan 2025; AzTrials last refreshed its copy on 8 Nov 2026.

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