Inclusion criteria | |
i | Patients selected for or that underwent coronary artery bypass surgery (CABG), a fractional flow reserve test (FFR) and/or a percutaneous coronary intervention (PCI), an electrophysiological test (EFO) and/or radiofrequency catheter ablation (RFCA), a transcatheter aortic valve implantation (TAVI), and/or valve surgery |
ii | Age ≥ 18 years |
iii | Able to speak and read the Dutch language |
iv | Willing and able to provide informed consent |
Exclusion criteria | |
i | No internet connection at home |
ii | Not in possession of a computer or tablet; and mobile phone |
iii | Not able or willing to wear activity tracker on a daily basis (for example due to work related obligations) |
iv | Major planned (cardiac) surgery in the upcoming 3 months |
v | Life expectancy < 1 year (e.g., severe renal disease, metastatic cancer) |
vi | Physical impairments interfering with the lifestyle monitoring system, including not able to perform daily physical activities due to orthopedic or neurological disease, bed/chair ridden patients, visual impairments/blindness, severe cognitive disability |
vii | Presence of wounds, injuries or infectious diseases on the skin where the wrist-wearable device(s) will be placed |
viii | Mentally incompetent |