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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)

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
Unknown
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON37248
Enrollment
1000
Registered
2013-03-22
Start date
Unknown
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

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: age 18-80 years hospitalized for an acute coronary syndrome less than 8 weeks before inclusion , 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, percutaneous coronary intervention or other interventions expected within 8 weeks after inclusion - limited life expectancy (*2 years) - New York Heart Association class III or IV heart failure - Beck's Depression Inventory (BDI) score of *10

Design outcomes

Primary

MeasureTime 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

MeasureTime frame
Comparison between baseline and 12 months of: * Smoking status (urinary cotinine

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)