Study design:
Prospective observational study
Sample size:
120 Participants
Study Sites:
Bispebjerg Hospital, Rigshospitalet & Region Hovedstadens Akutberedskab
Inclusion criteria:
– Adult patients (≥18 years) admitted (with at least one night stay) with an acute medical or surgical disease and scheduled for discharge to their own homes
-Adult patients (≥18 years) who have contacted the EMS and, after assessment by paramedic personnel, not deemed sick enough for immediate hospital admission.
Study Procedures:
The study aims to investigate the use of wireless, continuous monitoring in patients at home including the frequency of alarms triggered by abnormal vital parameters and their significance for (re)hospitalisation/Serious
Adverse Events(SAE) and/or death within 30 days.
Outcome:
(re)hospitalisation/Serious Adverse Events(SAE) and/or death within 30 days.
Primary Investigators:
Emilie Sigvardt, MD
NCT:
NCT06077851