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Effects of a nurse coordinated program of lifestyle improvement aimed at reducing the risk of recurrent cardiovascular events in patients who have suffered an acute coronary syndrome. RESPONSE2: (Randomised Evaluation of Secondary Prevention by Outpatient Nurse SpEcialists 2).

Completed
Conditions
atherosclerosis
cardiovascular diseases
10011082
10024450
Registration Number
NL-OMON53161
Lead Sponsor
Academisch Medisch Centrum
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
1000
Inclusion Criteria

age *18 years
hospitalized for an acute coronary syndrome less than 8 weeks before inclusion or patients who have recently undergone coronary artery bypass surgery or a (first) percutaneous coronary intervention less than 8 weeks before inclusion and at least one of the following lifestyle related risk factors:
- Smoking (including smoking of any tobacco product in the 6 months preceding hospitalisation).
- BMI- 27 kg/m2
- Physical activity below recommended levels (5 times 30 minutes/week)

Exclusion Criteria

- visits to the prevention programs not feasible
- not available for follow-up
- surgery (coronary arterial bypass graft) expected within 8 weeks after inclusion
- limited life expectancy (-2 years)
- New York Heart Association class III or IV heart failure
- Hospital Anxiety and Depression score of -14 or greater

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The following parameters are compared between the intervention group and the<br /><br>control group at 12 months:<br /><br>* Smoking status (binary, non-smoking is defined as urinary cotinine < 200<br /><br>ng/ml)<br /><br>* Body Mass Index (kg/m2)<br /><br>* 6 Minute Walking Distance (meters)</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>Comparison between baseline and 12 months of:<br /><br>* Smoking status (urinary cotinine < 200 ng/ml)<br /><br>* Body Mass Index (kg/m2)<br /><br>* Waist circumference (cm)<br /><br>* 6 Minute Walking Distance (meters)<br /><br><br /><br>2. The following parameters are compared between the intervention group and the<br /><br>control group at 12 months:<br /><br>* fasting serum LDL levels (mmol/L)<br /><br>* systolic blood pressure (mmHg)<br /><br>* incidence of newly diagnosed diabetes mellitus<br /><br>* control of existing diabetes mellitus (fasting blood glucose and plasma HbA1c<br /><br>levels)<br /><br>* body composition (fat and muscle mass by impedance scales)<br /><br>* hospital readmission rates<br /><br>* signs of depression (Hospital Anxiety and Depression score)</p><br>
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