Cardiovascular Health Assessment of Preterm- and TERm-born Children
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Premature Birth. Basic parameters: 3 years — 9 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United Kingdom
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
The purpose of the CHAPTER study is to help understand how complications during pregnancy, such as preterm birth, affect how childrens' hearts and blood vessels develop.
Detailed description
Young adults born preterm (less than 37 weeks gestation) have alterations in the structure and function of the heart, with similar changes observed in preterm infants in the first three months of life. It is unknown whether these early changes in the heart seen in the first few months of life are relevant to long-term changes in heart structure and function. Heart changes have also not been well studied in children born preterm. To investigate this, the study will follow up children from the EPOCH study and will perform two study visits for each child (n=100 preterm and n=100 term) that will use echocardiography and cardiovascular magnetic resonance. Individuals in the EPOCH study had echocardiography measures done at birth and three months postnatal age. It will therefore be possible to do longitudinal echocardiography measures from birth up to ages 12 years to determine whether postnatal heart changes in preterm infants track into childhood. Cardiovascular magnetic resonance will allow for the determination of whether these early heart changes influence heart pump function. Finally, by measuring lung function, blood vessel structure and function, and blood pressure, it will be possible to determine how heart changes relate to other components of the cardiovascular system. This data will be used to confirm the relevance of early heart remodelling in preterm-born offspring over time and provide more comprehensive heart phenotyping for preterm-born children. Together, this information can be used to design future intervention strategies in preterm-born individuals to reduce cardiovascular risk in this growing subgroup of the population.
Primary outcome measures
- Cardiac left ventricular mass [Time frame: 3-5 years of age OR 8-12 years of age; AND 6-9 years of age]
Secondary outcome measures (12)
- Cardiac right ventricular mass [Time frame: 3-5 years of age OR 8-12 years of age; AND 6-9 years of age]
- Cardiac left ventricular end-diastolic volume [Time frame: 3-5 years of age OR 8-12 years of age; AND 6-9 years of age]
- Cardiac right ventricular end-diastolic volume [Time frame: 3-5 years of age OR 8-12 years of age; AND 6-9 years of age]
- Cardiac left ventricular systolic function [Time frame: 3-5 years of age OR 8-12 years of age; AND 6-9 years of age]
- Cardiac right ventricular systolic function [Time frame: 3-5 years of age OR 8-12 years of age; AND 6-9 years of age]
- Cardiac left ventricular diastolic function [Time frame: 3-5 years of age OR 8-12 years of age; AND 6-9 years of age]
- Cardiac right ventricular diastolic function [Time frame: 3-5 years of age OR 8-12 years of age; AND 6-9 years of age]
- Morphology of the left ventricles [Time frame: 6-9 years of age]
- Morphology of the right ventricles [Time frame: 6-9 years of age]
- Cardiac flow dynamics of the left ventricle [Time frame: 6-9 years of age]
- Systolic blood pressure measurement [Time frame: 3-5 years of age OR 8-12 years of age; AND 6-9 years of age]
- Diastolic blood pressure measurement [Time frame: 3-5 years of age OR 8-12 years of age; AND 6-9 years of age]
Eligibility criteria
Inclusion criteria
- Participant's parent or legal guardian gives consent and the participant, where age-appropriate, gives assent for participation in the study.
- Participant is male or female, aged 3-9 years at enrolment.
- Participant previously took part in the EPOCH study, or the participant's friend or sibling took part.
Exclusion criteria
- Evidence of congenital heart disease or significant chronic disease relevant to cardiovascular or metabolic status
For exclusion of MRI component only:
- Contraindication to MRI
- Unsuitable for MRI based on the responses to the MRI screening form
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Study design
- Observational model
- Case-control
Study locations
United Kingdom · 1 center
- University of Oxford — Oxford
Identifiers
NCT: NCT05698836 · 18/WM/0131