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).

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). - RESPONSE 2

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON53161

Enrollment

1000

Registered

2013-03-22

Start date

2013-04-22

Completion date

Unknown

Last updated

2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

atherosclerosis cardiovascular diseases

Interventions

On top of usual care, the intervention group will receive a comprehensive, modular, tailored lifestyle intervention, involving the partner where appropriate, using e-health support and referral to e

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

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

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

Design outcomes

Primary

Measure	Time frame
The following parameters are compared between the intervention group and the control group at 12 months: * Smoking status (binary, non-smoking is defined as urinary cotinine	—

Secondary

Measure	Time frame
Comparison between baseline and 12 months of: * Smoking status (urinary cotinine	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)