Hypertension Clinical Trial
Official title:
Educore Project: A Clinical Trial, Randomised by Clusters, to Assess the Effect of a Visual Learning Method on Blood Pressure Control in the Primary Health Care Setting
Background: High blood pressure (HBP) is a major risk factor for cardiovascular disease
(CVD). European hypertension and cardiology societies as well as expert committees on CVD
prevention recommend stratifying cardiovascular risk (CVR) using the SCORE method, the
modification of lifestyles to prevent CVD, and achieving good control over risk factors. The
EDUCORE (Education and Coronary Risk Evaluation) project aims to determine whether the use of
a CVR visual learning method - the EDUCORE method - is more effective than normal clinical
practice in improving the control of blood pressure within one year in patients with poorly
controlled hypertension but no background of CVD.
Design & Method: Cluster randomized controlled clinical trial. Location: 22 primary health
care centres in Madrid. Participants: patients diagnosed as hypertensive (systolic >140 mmHg
and/or diastolic >90 mmHg) at least a year before, uncontrolled. Age: 40-65 year-old patients
who consent to take part. Sampling: randomized cluster assignment. Random allocation unit:
health care centre. Analysis unit: patient who match criteria. Size: 736 patients (368 each
arm. Measurements: Outcome variables: systolic and diastolic blood pressure (mmHg).
Cardiovascular risk level: SCORE. Measure of Adherence to treatment (Morisky-Green
questionnaire. Health related quality of life questionnaire MINICHAL. Smoking habits. Total
Cholesterol. Other variables: Gender. Age. Educational level. Physical activity in metabolic
equivalent (MET). Body mass index. Drug consume (cardiovascular line). Treatment changes and
nature of the change. Intervention: EDUCORE group (direct exhibition of their cardiovascular
risk with SCORE, visual images and documentation to the patients); Control Group: standard
practice care.
Aim: To measure the effectiveness of an educational intervention in uncontrolled hypertensive
patients without cardiovascular disease (primary prevention), compared with clinical practice
to improve hypertension control in a year.
Method: This work describes a protocol for a clinical trial, randomised by clusters and
involving 22 primary healthcare clinics (PHCC), to test the effectiveness of the EDUCORE
method. The number of patients required was 736, all between 40 and 65 years of age (n=368 in
the EDUCORE and control groups), all of whom had been diagnosed with HBP at least one year
ago, and all of whom had poorly controlled hypertension (systolic blood pressure ≥ 140 mmHg
and/or diastolic ≥ 90 mmHg). All personnel taking part were explained the trial and trained
in its methodology. The EDUCORE method contemplates the visualisation of low risk SCORE
scores using images embodying different stages of a high risk action, plus the receipt of a
pamphlet explaining how to better maintain cardiac health. The main outcome variable was the
control of blood pressure; secondary outcome variables included the SCORE score, therapeutic
compliance, quality of life, and total cholesterol level. All outcome variables were measured
at the beginning of the experimental period and again at 6 and 12 months. Information on sex,
age, educational level, physical activity, body mass index, consumption of medications,
change of treatment and blood analysis results was also recorded.
Information source: Clinical interview and assessments tests. The data will be registered in
Electronic data capture system.
Statistical Analysis: Primary and secondary effectiveness. Adjusting by prognosis factors
with random effects models (logistic regression) (dependent variable: good/bad blood pressure
control; independent variable: intervention group).
Discussion: The EDUCORE method could provide a simple, inexpensive means of improving blood
pressure control, and perhaps other health problems, in the primary healthcare setting.
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