Tests feedback and support to improve cardiac rehabilitation programs after heart attack
Tests feedback and support for rehabilitation centers treating adults after a heart attack.
Plain-language title generated from the registry record
Registry title: The Perfect-CR Implementation Study
Key facts
- Where
- Malmö, SwedenSee the site
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 18 and 79 years old?
Source: NCT05889416, who can take part
Where in Sweden
- Skåne University HospitalMalmö, SwedenNo longer taking part
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Skane University Hospital
- Trial code
- NCT05889416
- Record updated
- 29 November 2024
- Original description
The goal of this open-label cluster-randomized effectiveness-implementation hybrid trial is to study whether a) audit and feedback of cardiac rehabilitation service delivery within a national quality registry and b) structured implementation support can improve center-level adherence to guidelines and short and long-term patient-level outcomes.Read full original descriptionShow less
The Effect of Audit and Feedback Within a National Registry and Implementation Support on Guideline Adherence and Patient Outcomes in Cardiac Rehabilitation: an Open-label Cluster-randomized Effectiveness-implementation Hybrid Trial
The goal of this open-label cluster-randomized effectiveness-implementation hybrid trial is to study whether a) audit and feedback of cardiac rehabilitation service delivery within a national quality registry and b) structured implementation support can improve center-level adherence to guidelines and short and long-term patient-level outcomes.
Inclusion: Centres report to the SWEDEHEART registry; Diagnosis of a type 1 MI registered in the SWEDEHEART registry; Age 18-79 years at discharge from hospital; Attended at least two follow-up visits at CR centres included in the study.
Exclusion: Unwillingness to participate in the study; Patient-level; None.
Centre-level.