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Clinical Trials/NCT02486913
NCT02486913CompletedNot 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 enrollmentStarted: August 1, 2015Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
190
Locations
1
Primary Endpoint
Change in Heart Age

Study 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.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
40 Years to 74 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Adults aged 40-74 years

Exclusion Criteria

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

Arms & Interventions

Conventional Health Check

No Intervention

Patients undergoing conventional National Health Service Health Check

Enhanced Health Check

Experimental

Patients undergoing National Health Service Health Check enhanced by risk report

Intervention: Enhanced Health Check (Other)

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)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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