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Clinical Trials/NCT02486913
NCT02486913
Completed
Not Applicable

Enhancing the Diagnosis and Prevention of Cardiovascular Disease in Newham by Integrated Use of Electronic Health Records

Queen Mary University of London1 site in 1 country190 target enrollmentAugust 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiovascular Disease
Sponsor
Queen Mary University of London
Enrollment
190
Locations
1
Primary Endpoint
Change in Heart Age
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The investigators will develop a "risk report" within the primary care electronic health record (EMIS) for patients attending for their National Health Service Health Check. The value of the report for reducing cardiovascular risk will be assessed qualitatively and also quantitatively in a non-randomised comparative trial.

Detailed Description

The investigators will design a template within the primary care electronic health record (EMIS) that draws on Health Check data to provide a contemporary "risk report". Included in the report will be clear description of life-time cardiovascular risks, the factors driving those risks and how risk might be reduced through life-style and risk factor modification. The investigators will evaluate the benefits of providing patients with a risk report qualitatively by patient and clinician interviews. Quantitative analysis of the benefit of the risk report will be provided by a non-randomised comparative trial. First, a group of patients undergoing a conventional Health Check will be recalled after three months for a second Health Check, allowing measurement of the change in "Heart Age" - a convenient index of life-time cardiovascular risk. Following introduction of the risk report the investigators will recall a further group of patients for a second Health Check, allowing measurement of the change in "Heart Age". The effect of the risk report will be determined by comparing the change in Heart Age between the two groups of patients.

Registry
clinicaltrials.gov
Start Date
August 2015
End Date
January 1, 2018
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adults aged 40-74 years

Exclusion Criteria

  • Prior diagnosis of heart disease, stroke, diabetes, kidney disease or dementia

Outcomes

Primary Outcomes

Change in Heart Age

Time Frame: 3 months

Change in Heart Age between 1st Health Check and 2nd Health Check three months later

Secondary Outcomes

  • Change in systolic blood pressure(3 months)
  • Change in total cholesterol(3 months)
  • Changes in smoking status(3 months)
  • Change in body mass index(3 months)

Study Sites (1)

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