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Enrolling by invitationNo phase

Registry following cardiac rehabilitation programs in low-resource settings

Records how heart rehabilitation is delivered and how patients with heart disease fare.

Plain-language title generated from the registry record
Registry title: International CR Registry

Key facts

Where
Doha, QatarSee the site

Where in Qatar

  • Hamad Medical CorporationDoha, QatarNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
University Health Network, Toronto
Trial code
NCT04676100
Record updated
4 December 2023
Original description
The ICRR is a health services registry to establish the quality of CR delivery, and the effectiveness in terms of patient outcomes, in low-resource settings. The purposes of the registry are care optimization, evidentiary support for CR advocacy / policy, and research.Read full original descriptionShow less

International Cardiac Rehabilitation Registry (ICRR) Protocol

The ICRR is a health services registry to establish the quality of CR delivery, and the effectiveness in terms of patient outcomes, in low-resource settings. The purposes of the registry are care optimization, evidentiary support for CR advocacy / policy, and research.

All programs in low-resource settings will be welcome to participate at no cost. Programs will follow procedures approved by their local ethics board for collection of program and patient-reported variables. Assessments occur pre-cardiac rehabilitation (CR), post-CR and annually thereafter.

Inclusion: SITES:; CR program (defined in intervention section); in low-resource setting (i.e., low or middle-income country according to World Bank, or in region within a higher-income country where there is under-development of CR related to financial resources, lack of healthcare system resources, lack of patient and provider awareness, and/or patient disadvantage [e.g., limited social resources, geographic barriers]).

Exclusion: SITES:; -program cannot enter data in English; PATIENTS:; not capable to understand the registry information letter for cognitive or mental reasons (although they would also likely be excluded from CR); not proficient in the language of the local ethics-approved registry information letter /consent form.

ClinicalTrials.gov NCT04676100