- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05955456
Detecting EARLY Heart Failure in Greater Manchester (EARLY-HF)
Detecting EARLY Heart Failure in Greater Manchester (EARLY-HF)
Heart failure represents a growing public health problem within the UK and particularly within the North West of England. A major challenge is that heart failure is currently diagnosed too late.
The researchers have previously developed a risk calculator that accurately identifies individuals at risk of heart failure admission or death before they have developed heart failure.
Most risk calculators are never implemented into clinical practice. The researchers will l perform a pilot study to evaluate the risk calculator within primary care in Greater Manchester.
Study Overview
Detailed Description
The researchers have previously developed and externally validated a novel multimodal risk calculator that accurately identifies individuals at-risk of heart failure admission or death before they have developed heart failure. This risk calculator includes key co-morbidities, circulating biomarkers and cardiac magnetic resonance imaging (CMR) measurements of cardiac structure and function. It identifies those individuals at highest risk of developing heart failure and therefore those who may most benefit from targeted cardiometabolic therapeutics in the future.
The researchers will l perform a pilot study to evaluate the risk calculator within primary care in Greater Manchester. A qualitative and quantitative assessment of risk calculator uptake will be performed within local GP practices and primary care populations. The research team will determine how effectively they can recruit participants from socioeconomically deprived and ethnically diverse backgrounds. A preliminary analysis will be performed to determine risk calculator accuracy within a prospective primary care cohort, and dynamically refine the model aiming to improve performance. The study will also involve conducting an initial cost effectiveness analysis to determine the real-world economic impact of model implementation.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
-
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Greater Manchester
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Manchester, Greater Manchester, United Kingdom, M13 9WL
- Recruiting
- Manchester University NHS Foundation Trust
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Contact:
- Nicholas Black, BM BCh
- Phone Number: 0161 291 4075
- Email: nicholas.black@mft.nhs.uk
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Written informed consent
- Aged 50 and over
- Two or more of the following conditions: type 2 diabetes, chronic obstructive pulmonary disease, ischaemic heart disease, atrial fibrillation, hypertension, chronic kidney disease stage 3, body mass index ≥ 30 kg/m2
Exclusion Criteria:
- Established diagnosis of one or more of the following: heart failure, cardiomyopathy, moderate or severe valvular heart disease, congenital heart disease, heart transplant, idiopathic, heritable or drug-induced pulmonary arterial hypertension, any medical condition, which in the opinion of the Investigator, may place the patient at higher risk from his/her participation in the study, or is likely to prevent the patient from complying with the requirements of the study or completing the study.
- Contraindication to cardiovascular magnetic resonance (CMR) scanning, including pacemaker, defibrillator, intraocular metal, intracranial aneurysm clips, severe claustrophobia, estimated glomerular filtration rate < 30 ml/min/1.73m2, previous severe allergic reaction or anaphylaxis to gadolinium-based contrast agent, pregnancy or breastfeeding.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Participants in primary care with risk factors for heart failure
|
No intervention is applied to participants.
The risk calculator score is not released to the participants or care providers.
Participants are followed up for risk calculator accuracy and recalibration.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Preliminary measures of risk calculator validation and accuracy in Greater Manchester
Time Frame: 5 years
|
Risk calculator will predict incident heart failure, first heart failure hospitalisation, cardiovascular death and all cause death
|
5 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Qualitative measures of primary care uptake and engagement
Time Frame: 5 years
|
Number of participant identification sites, methods of participant identification, proportion of eligible participants contacted and recruited
|
5 years
|
|
Proportion of participants recruited from socioeconomically deprived and ethnically diverse backgrounds
Time Frame: 5 years
|
Ability to recruit participants from socioeconomically deprived and ethnically diverse backgrounds within Greater Manchester
|
5 years
|
|
Measures of prognostic model calibration and discrimination in a primary care population
Time Frame: 5 years
|
Examples include calibration slope, intercept and Harrell's C statistic
|
5 years
|
|
Measures of prognostic model optimisation and accuracy with iterative variable inclusion or exclusion
Time Frame: 5 years
|
Assess variable inclusion and exclusion using stepwise model selection and Wald statistic
|
5 years
|
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Causal statistical analysis to determine effect of hypothetical interventions
Time Frame: 5 years
|
Mediation analysis to determine causative effects of hypothetical interventions
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5 years
|
|
Measures of cost effectiveness of the model in Greater Manchester
Time Frame: 5 years
|
Examples include decision curve analysis
|
5 years
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- B01899
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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