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Clinical Trials/ACTRN12608000182392
ACTRN12608000182392Completed未知

For patients who survive acute coronary syndrome does the availability of the CHOICE (Choice of health options in prevention of cardiovascular events) program improve the uptake of secondary prevention and reduce the proportion of patients with risk factors above national targets.

ANZAC Research Institute, Concord Hospital0 sites500 target enrollmentStarted: April 10, 2008Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
500

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional
Allocation
Randomised controlled trial
Primary Purpose
Prevention
Masking
Blinded (masking used)

Eligibility Criteria

Ages
18 Years to o limit (—)
Sex
All

Inclusion Criteria

  • Diagnosis of ACS in the four weeks prior to recruitment; refusal of the initial invitation to participate in standard CR; failure to attend initial CR assessment.

Exclusion Criteria

  • Clinical diagnosis of uncompensated, severe cardiac failure (Class IV); uncontrolled arrhythmia or angina; severe or symptomatic aortic stenosis; persistent hypotension (SBP < 90mmHg); clinical diagnosis of a severe coexisting medical condition that would prevent participation (eg, dementia, a terminal illness, severe rheumatoid arthritis); or insufficient English to provide written informed consent.

Investigators

Sponsor
ANZAC Research Institute, Concord Hospital

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