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.
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.
United States1 site, 1 recruiting
- 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
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:
- multidisciplinary (OB/maternal-fetal medicine [MFM], cardiology, anesthesia, critical care, etc.) care teams;
- a COB care coordinator;
- coordinated inter-disciplinary patient evaluation;
- team debriefing
- the ability to perform high-risk deliveries in the ICU and
- 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.
- Conditions
- Pregnancy Complications, Cardiovascular
- 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 group | Role | What they receive |
|---|---|---|
| Pregnant people with cardiovascular disease | Any 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.
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)
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
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.
- First posted24 Jul 2024
- Study start14 Jan 2025
- Primary completion30 Jun 2028 (estimated)
- Study completion30 Jun 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Pregnancy Complications, CardiovascularStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- University of Missouri, Kansas City
- Sponsor type
- University, hospital or other
- Collaborators
- Albert Einstein College of Medicine, Baylor College of Medicine, Beth Israel Deaconess Medical Center, The Children's Hospital Corporation, The Brigham and Women's Hospital, Inc., Columbia University, Henry Ford Hospital, The Johns Hopkins University, The Miriam Hospital/Lifespan, Massachusetts General Hospital, Northwell Health, Northwestern University, Oregon Health and Science University, Saint Luke's Health System, Board of Trustees of the Leland Stanford Junior University, The Research Foundation for the State University of New York, The Regents of the University of California, Irvine, The Regents of the University of California, Los Angeles, University of North Carolina, Chapel Hill, The Board of Trustees of the University of Illinois, Trustees of Indiana University, University of Kansas Medical Center, University of Massachusetts, Worcester, University of Michigan, University of Mississippi Medical Center, The Curators of the University of Missouri, The Trustees of the University of Pennsylvania, University of Pittsburgh, University of South Florida, University of Washington, University of Texas Southwestern Medical Center, Weil Medical Colleqe of Cornell University, Women and Infants Hospital of Rhode Island, Tennessee Maternal Fetal Medicine PLC
- Responsible party
- Sponsor
- Investigators
- John Spertus, MD, MPH, Principal investigator, University of Missouri, Kansas City
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.
Study at a glance
From the registry record, last updated by the sponsor on 20 Jan 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Heart Outcomes in Pregnancy Expectations for Mom and Baby Study
- ClinicalTrials.gov ID
- NCT06517628
- Acronym / sponsor ID
- HOPE / 0073599
- Conditions
- Pregnancy Complications, Cardiovascular
- Keywords
- Pregnancy, cardio-obstetrics, Structures of Care, Quality of Care, Disparities, Heart disease in pregnancy, Pregnancy complications, Adverse pregnancy outcomes, Major adverse cardiac events
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 1,000 participants (estimated)
- Lead sponsor
- University of Missouri, Kansas CityUniversity, hospital or other
- Collaborators
- Albert Einstein College of Medicine, Baylor College of Medicine, Beth Israel Deaconess Medical Center, The Children's Hospital Corporation, The Brigham and Women's Hospital, Inc., Columbia University, Henry Ford Hospital, The Johns Hopkins University, The Miriam Hospital/Lifespan, Massachusetts General Hospital, Northwell Health, Northwestern University, Oregon Health and Science University, Saint Luke's Health System, Board of Trustees of the Leland Stanford Junior University, The Research Foundation for the State University of New York, The Regents of the University of California, Irvine, The Regents of the University of California, Los Angeles, University of North Carolina, Chapel Hill, The Board of Trustees of the University of Illinois, Trustees of Indiana University, University of Kansas Medical Center, University of Massachusetts, Worcester, University of Michigan, University of Mississippi Medical Center, The Curators of the University of Missouri, The Trustees of the University of Pennsylvania, University of Pittsburgh, University of South Florida, University of Washington, University of Texas Southwestern Medical Center, Weil Medical Colleqe of Cornell University, Women and Infants Hospital of Rhode Island, Tennessee Maternal Fetal Medicine PLC
- Study start
- 14 Jan 2025 (actual)
- Primary completion
- 30 Jun 2028 (estimated)
- Study completion
- 30 Jun 2028 (estimated)
- First posted
- 24 Jul 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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:
- multidisciplinary (OB/maternal-fetal medicine [MFM], cardiology, anesthesia, critical care, etc.) care teams;
- a COB care coordinator;
- coordinated inter-disciplinary patient evaluation;
- team debriefing
- the ability to perform high-risk deliveries in the ICU and
- 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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Pregnant people with cardiovascular disease | – | Other: Purely observational study on the care and outcomes of participants with cardiovascular disease in pregnancy.Any pregnant patient with acquired or congenital cardiovascular disease upon presentation to a cardio-obstetrics clinic. |
Who may qualify
- Ages
- 18 years and older
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Pregnant people with cardiovascular disease
Key inclusion criteria (7 listed)
- 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
Key exclusion criteria (9 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Purely observational study on the care and outcomes of participants with cardiovascular disease in pregnancy.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. | Other | Pregnant people with cardiovascular disease |
Primary outcome
Rate of Adverse pregnancy outcomes
Time frame: up to 6 weeks postpartum
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
2 secondary outcomes
Rate of Maternal Adverse Cardiac Events (MACE)
Time frame: Up to 1 year postpartum
Rate of Neonatal adverse clinical events (NACE)
Time frame: Through maternal hospital discharge
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Jan 2025.
- Individual participant dataSharing planned: 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.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
John Spertus, MD, MPH principal investigator
University of Missouri, Kansas City
1 site in 1 country: see every site and its status.
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.