MyoFit46: MultiMorbidity Life-Course Approach To Myocardial Health -A Cardiac Sub-Study of the MRC National Survey of Health and Development (NSHD)

Sponsor
University College, London (Other)
Overall Status
Recruiting
CT.gov ID
NCT05455125
Collaborator
(none)
550
1
48
11.5

Study Details

Study Description

Brief Summary

Background The life course accumulation of overt and subclinical myocardial dysfunction contributes to older age mortality, frailty, disability and loss of independence. The Medical Research Council National Survey of Health and Development (NSHD) is the world's longest running continued surveillance birth cohort providing a unique opportunity to understand life course determinants of myocardial dysfunction as part of MyoFit46-the cardiac sub-study of the NSHD.

Methods and expected results The investigators aim to recruit 550 NSHD participants of approximately 75 years+ to undertake high-density surface electrocardiographic imaging (ECGI) and stress perfusion cardiovascular magnetic resonance (CMR). Through comprehensive myocardial tissue characterization and 4-dimensional flow the investigators hope to better understand the burden of clinical and subclinical cardiovascular disease. Supercomputers will be used to combine the multi-scale ECGI and CMR datasets per participant. Rarely available, prospectively collected whole-of-life data on exposures, traditional risk factors and multimorbidity will be studied to identify risk trajectories, critical change periods, mediators and cumulative impacts on the myocardium.

Conclusion By combining well curated, prospectively acquired longitudinal data of the NSHD with novel CMR-ECGI data and sharing these results and associated pipelines with the CMR community, MyoFit46 seeks to transform our understanding of how early, mid and later-life risk factor trajectories interact to determine the state of cardiovascular health in older age.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: CMR CGI

Study Design

Study Type:
Observational
Anticipated Enrollment :
550 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
A Cardiac Sub-Study of the MRC National Survey of Health and Development (NSHD)
Actual Study Start Date :
Jul 1, 2020
Anticipated Primary Completion Date :
Jun 30, 2024
Anticipated Study Completion Date :
Jun 30, 2024

Outcome Measures

Primary Outcome Measures

  1. CMR phenotype - T1 [Through study completion, an average of 4 years.]

    This will be assessed through a 45 minute cardiac MRI scan with perfusion.

  2. CMR phenotype - T2 [Through study completion, an average of 4 years.]

    This will be assessed through a 45 minute cardiac MRI scan with perfusion.

  3. CMR phenotype - Myocardial blood flow [Through study completion, an average of 4 years.]

    This will be assessed through a 45 minute cardiac MRI scan with perfusion.

  4. CMR phenotype - Aortic blood flow [Through study completion, an average of 4 years.]

    This will be assessed through a 45 minute cardiac MRI scan with perfusion.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • NSHD study member.

  • Who is still alive and agreed to take part in the study.

Exclusion Criteria:
  • Pacemaker.

  • Implantable cardio defibrillator.

  • Atrial fibrillation.

  • Complete heart block.

  • Severe asthma.

Contacts and Locations

Locations

Site City State Country Postal Code
1 UCL Bloomsbury Centre for Clinical Phenotyping London United Kingdom SW13 0JD

Sponsors and Collaborators

  • University College, London

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University College, London
ClinicalTrials.gov Identifier:
NCT05455125
Other Study ID Numbers:
  • 123172
First Posted:
Jul 13, 2022
Last Update Posted:
Jul 13, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 13, 2022