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Streamlining follow up of intermediate risk chest pain presentations: Does pre-organised early stress testing improve compliance to guidelines and 30-day outcomes?

Not Applicable
Conditions
Intermediate risk of non-ST-elevation acute coronary syndrome
Cardiovascular - Coronary heart disease
Public Health - Health promotion/education
Registration Number
ACTRN12611000470998
Lead Sponsor
A/Prof David Playford
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
120
Inclusion Criteria

>18 yo and informed consent obtained, discharged from emergency department with intermediate risk acute coronary syndrome, suitable for exercise threadmill stress testing, able to follow up patient via telephone at 30 days.

Exclusion Criteria

Pregnancy, contraindications to stress testing, <18 yo or >75 yo, cognitively impaired, inability to consent, inability to follow up patient (overseas visitor or no telephone access)

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To determine whether providing patients with pre-organised appointment times increases their compliance to return for exercise stress testing.[Follow up will occur at day 30 post discharge from the emergency department in order to evaluate their compliance with attending exercise stress testing]
Secondary Outcome Measures
NameTimeMethod
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