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Clinical Trials/NL-OMON53161
NL-OMON53161
Completed
Not Applicable

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

Academisch Medisch Centrum0 sites1,000 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
atherosclerosis
Sponsor
Academisch Medisch Centrum
Enrollment
1000
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Eligibility 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

  • \- 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

Outcomes

Primary Outcomes

Not specified

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