Design of a randomized controlled trial of comprehensive rehabilitation in patients with myocardial infarction, stabilized acute coronary syndrome, percutaneous transluminal coronary angioplasty or coronary artery bypass grafting: Akershus Comprehensive Cardiac Rehabilitation Trial (the CORE Study)

Autor: Karin Kogstad Else; Erikssen Jan; Sandvik Leiv; Rollag Arnfinn; Ditlef Jacobsen Carl; Pater Cornel
Sprache: Englisch
Veröffentlicht: 2000
Quelle: Directory of Open Access Journals: DOAJ Articles
Online Zugang: http://cvm.controlled-trials.com/content/1/3/177
https://doaj.org/toc/1468-6708
doi:10.1186/cvm-1-3-177
1468-6708
https://doaj.org/article/3353359b35654e91acda2c27bc451d63
https://doi.org/10.1186/cvm-1-3-177
https://doaj.org/article/3353359b35654e91acda2c27bc451d63
Erfassungsnummer: ftdoajarticles:oai:doaj.org/article:3353359b35654e91acda2c27bc451d63

Zusammenfassung

Abstract Objectives 1. To assess the long-term effectiveness of a comprehensive cardiac rehabilitation programme on quality of life and survival in patients with a large spectrum of cardiovascular diseases (myocardial infarction, acute coronary syndrome, percutaneous transluminal coronary angioplasty and coronary artery bypass grafting). 2. To establish the degree of correlation between expected improvement of health-related quality of life and improvement in physical function attributable to rehabilitation in the intervention group, in comparison with similar changes in the conventional care group. Design Randomized, controlled, parallel-group design (intervention/conventional care). Setting Akershus County, southeast of Oslo City, Norway. Participants 500 patients, men and women, aged 40-85 years, who have sustained at least one of the above-mentioned cardiovascular diseases. Interventions 8 weeks of supervised, structured physical training of three periods of 20 min per week, targeting a heart rate of 60-70% of the individual's maximum; home-based physical exercise training with the same basic schedule as in the supervised period; quantification of patients' compliance with the exercise programme by the use of wristwatches, information stored in the watch memory being retrieved once a month during the 3-year follow-up period; and life-style modification with an emphasis on the cessation of smoking and on healthy nutrition and weight control.