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Randomised Evaluation of Secondary Prevention by Outpatient Nurse SpEcialists

Randomised Evaluation of Secondary Prevention by Outpatient Nurse SpEcialists - RESPONSE

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON30357
Enrollment
1000
Registered
2006-06-01
Start date
2006-01-06
Completion date
Unknown
Last updated
2024-06-18

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

Conditions

None listed

Interventions

Patients randomised to the intervention group will, in addition to usual care, be seen at the NLPC. Here they receive counselling and support to promote a healthy lifestyle, including cessation of s

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: • Age 18-80 years • Hospitalisation for an acute coronary syndrome (instabiele angina/acuut hartinfarct) less than 8 weeks before inclusion.

Exclusion criteria

Exclusion criteria: • Clinic visits not feasible • Not available for follow-up • Surgery/percutaneous coronary intervention expected within 8 weeks • Limited life expectancy • Previously enrolment in nurse-led prevention clinic • NYHA class 3 or 4 caused by heart failure

Design outcomes

Primary

MeasureTime frame
Change in status of Copenhagen Risk score and modifiable risk factors for coronary heart disease: smoking, exercise, excess weight, dyslipidaemia, hypertension, diabetes mellitus compared with group receiving usual care.

Secondary

MeasureTime frame
- Quality of life - Evaluation of efficiency of reaching treatment targets - Compliance with medical treatment - Risk scores: Europa-score, PROCAM-score, Euroscore

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)