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Clinical Trials/ISRCTN10054455
ISRCTN10054455
Completed
未知

Cardiac rehabilitation for people with chronic stable angina (ACTIVATE): a randomised controlled trial

niversity of Liverpool0 sites518 target enrollmentSeptember 16, 2021

Overview

Phase
未知
Intervention
Not specified
Conditions
Angina pectoris
Sponsor
niversity of Liverpool
Enrollment
518
Status
Completed
Last Updated
last year

Overview

Brief Summary

2024 Protocol article in https://pubmed.ncbi.nlm.nih.gov/38531561/ (added 27/03/2024)

Registry
who.int
Start Date
September 16, 2021
End Date
August 1, 2024
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversity of Liverpool

Eligibility Criteria

Inclusion Criteria

  • 1\. Aged \=18 years
  • 2\. Chronic stable angina with at least 2 out of 3 of the following features:
  • 2\.1\. Constricting central chest pain
  • 2\.2\. Precipitated by exertion or emotional stress
  • 2\.3\. Relieved by rest or glyceryl trinitrate spray
  • 3\. Documented coronary artery disease on angiography with \=70% stenosis of coronary arteries based on invasive coronary angiography, computerised tomography angiography, or reversible myocardial ischaemia on myocardial perfusion testing
  • 4\. Revascularisation procedures not planned and treated with medical treatments only. Including people with previous MI, or previous revascularisation procedure who may have attended cardiac rehabilitation in the past.

Exclusion Criteria

  • 1\. History of myocardial infarction (MI) within the last 12 months on electronic health record search
  • 2\. History of revascularisation procedure within the last 12 months, or planned at the time of study consent
  • 3\. Participation in cardiac rehabilitation programme within the last 12 months, or planned at time of study recruitment
  • 4\. Significant co\-morbidities (as deemed by person confirming eligibility) that would limit participation in the exercise based rehabilitation programme
  • 5\. Refractory angina on maximal medical therapy

Outcomes

Primary Outcomes

Not specified

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