Swiss Secondary Prevention and Rehabilitation Registry
Swiss Secondary Prevention and Rehabilitation Registry: SwissPR
University Hospital, Basel, Switzerland
4,000 participants
Dec 20, 2019
OBSERVATIONAL
Conditions
Summary
The SwissPR study is to continuously monitor patient characteristics and short- and long-term benchmark quality measures and outcomes of patients participating in a 12-week ambulatory CR program.
Eligibility
Inclusion Criteria2
- Participation in an ambulatory CR program (all age groups)
- Written informed consent
Exclusion Criteria4
- Inability to follow an ambulatory CR program more than 3 weeks
- Not willing to give informed consent
- Inability to understand the informed consent due to language comprehension
- Lack of discernment
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Interventions
Data collection (Patient characteristics including medical history, current medication, cardiovascular risk factors, routine laboratory analysis (including lipids, Hb1c, NT-proBNP), clinical status, electrocardiogram, echocardiography data from latest echo, cardio pulmonary exercise testing (CPET), questions on general health behavior (diet, weekly exercise load), Quality of Life and questions on socio-economic parameters)
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT05500859