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Evaluation of a programme of cardiovascular disease prevention in primary care

Not Applicable
Completed
Conditions
Cardiovascular disease
Circulatory System
Cardiovascular disease, unspecified
Registration Number
ISRCTN32114200
Lead Sponsor
niversity Hospitals Birmingham NHS Foundation Trust (UK)
Brief Summary

2016 results in https://www.ncbi.nlm.nih.gov/pubmed/27528707 2012 protocol in http://www.ncbi.nlm.nih.gov/pubmed/23101763

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
6250
Inclusion Criteria

Participating practices are identified by the participating primary care trusts.

Patients for inclusion in the prevention programme are identifed as follows. They must be registered at a participating practice. They must be aged between 35 and 74 and must not currently have coronary heart disease (CHD), not be on the diabetic register and not be currently receiving antihypertensive or statin treatment. From these patients are identified all those patients in whom a combination of risk factors indicates they are likely to be at greater than 20% ten-year risk of cardiovascular disease. These patients are considered eligible for inclusion in the cardiovascular prevention programme. These patients will be identified from primary care electronic medical records.

In summary:
1. Patients (both males and females) aged between 35 and 74
2. Patients who do not have CHD
3. Patients who are not diabetic
4. Patients who are not receiving antihypertensives or statins
5. Patients who are likely to be at greater than 20% ten-year CVD risk

Exclusion Criteria

Patients who in the opinion of the practice staff are unable to benefit from cardiovascular risk factor assessment. For example, patients who are terminally ill.

In practice this means that once a list has been created of individuals who are untreated high risk patients are eligible to be invited for cardiovascular risk factor assessment, practice staff will review the list and identify patients who are known to be terminally ill or otherwise unsuitable for inclusion.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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