- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05837364
Predicting Risk of Atrial Fibrillation and Association With Other Diseases (FIND-AF)
Risk of Atrial Fibrillation and Association With Other Diseases: Protocol of the Derivation and International External Validation of a Prediction Model Using Nationwide Population-based Electronic Health Records
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Atrial fibrillation (AF) is a major public health issue: it is increasingly common, incurs substantial healthcare expenditure, and is associated with a range of adverse outcomes. There is rationale for the early diagnosis of AF, before the first complication occurs. Previous AF screening research is limited by low yields of new cases and strokes prevented in the screened populations. For AF screening to be clinically and cost-effective, the efficiency of identification of newly diagnosed AF needs to be improved and the intervention offered may have to extend beyond oral anticoagulation for stroke prophylaxis. Previous prediction models for incident AF have been limited by their data sources and methodologies. An accurate model that utilises existing routinely-collected data is needed to inform clinicians of patient-level risk of AF, inform national screening policy and highlight opportunities to improve patient outcomes from AF screening beyond that of only stroke prevention.
The application of Random Forest will be investigated and multivariable logistic regression to predict incident AF within a 6 months prediction horizon, that is a time-window consistent with conducting investigation for AF. The Clinical Practice Research Datalink (CPRD)-GOLD dataset will be used for derivation, and the Clalit Health Services dataset will be used for international external geographical validation. Both comprise a large representative population and include clinical outcomes across primary and secondary care. Analyses will include metrics of prediction performance and clinical utility. Only risk factors accessible in the community will be used and the model could thus enable passive screening for high-risk individuals in electronic health records that is updated with presentation of new data. The study aims to create a calculator from a parsimonious model. Kaplan-Meier plots for individuals identified as higher and lower predicted risk of AF will be calculated and derive the cumulative incidence rate for non-AF cardio-renal-metabolic diseases and death over the longer term to establish how predicted AF risk is associated with a range of new non-AF disease states.
To ascertain whether the prediction model is transportable to geographies outside of the UK, the model's performance will be externally validated in the Clalit Health Services database in Israel. The validation will include participants insured by Clalit with continuous membership for at least 1 year before 01/01/2019: 2,159,663 patients with 4,330 of them having a new incident of AF (Atrial fibrillation and/or atrial flutter) in the first half of 2019. The study population will comprise all available patients who have at least 1-year follow up. The outcome of interest is the first diagnosed AF after baseline and will be identified using Read codes and ICD-9/10 codes. Patients with less than one year of registration, who are under thirty years of age at point of study entry, or have a preceding diagnosis of atrial fibrillation, will be excluded.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
West Yorkshire
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Leeds, West Yorkshire, United Kingdom, LS2 9NL
- University of Leeds
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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:
A least 1 year follow-up
Exclusion Criteria:
Diagnosed AF before study entry
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
1. To develop and validate a model for predicting the risk of new onset AF within the next 6 months
Time Frame: Between 1st Jan 1998 and 31st December 2018
|
a. Predictive factors will be identified using Read codes and ICD-9/10 codes (diagnoses) Variables considered as potential predictors may include sociodemographic variables (age, sex, ethnicity) and morbidities.
|
Between 1st Jan 1998 and 31st December 2018
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1. To quantify the association between risk of new-onset AF and the hazard of other cardio-renal-metabolic diseases and death
Time Frame: Between 1st Jan 1998 and 31st December 2018
|
a.
All patients categorized as lower or higher predicted AF risk by the developed prediction model will be included.
The initial presentation of a cardiovascular, renal, or metabolic disease or death will be considered because AF is associated with a high risk of adverse clinical outcomes.
The occurrence of death by any cause will be quantified.
Incident diagnoses will be defined as the first record of that condition in primary or secondary care records from any diagnostic position.
Kaplan-Meier plots will be created for individuals identified as higher and lower predicted risk of AF and derive the cumulative incidence rate for each outcome at 1, 5 and 10 years considering the competing risk of death, as well as death at 5 and 10 years.
For each specified outcome, the hazard ratio (HR) will be calculated between higher and lower predicted risk of AF using the Fine and Gray's model with adjustment for the competing risk of death.
|
Between 1st Jan 1998 and 31st December 2018
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Christopher P Gale, University of Leeds
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 318197
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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