Assessing the clinical and organisational impact of a home-based post-operative monitoring strategy incorporating the MultiSense® device involving 80 patients aged 65 years and over who have undergone major surgery.
Patient aged 65 or over
Patient eligible for remote monitoring using the MultiSense® device
No psychiatric illness that would prevent them from giving informed consent or receiving optimal treatment and follow-up care
Subject affiliated with a health insurance scheme
Patients already participating in an interventional clinical trial.
Patients subject to legal protection measures, guardianship, curatorship, or deprived of their liberty by judicial or administrative decision.
Patients hospitalised without consent.
Patients unable to complete a questionnaire and without a close relative to assist them in using the solution.
Rhythm Diagnostic Systems
Lead sponsor