Continuous Wireless Monitoring of Vital Signs and Automated Alerts in Participants at Home and During Hospitalization
Recruiting
Observational Study
Surgical Complication
Pulmonary Disease
Hematologic Diseases
Oncology
Cardiac Disease
Infections
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 3,095 (estimated)
- Sponsor
- University Hospital Bispebjerg and Frederiksberg · Other
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About This Trial
The primary aim of this study is to test and assess the implementation and effectiveness of continuous wireless vital signs monitoring with real-time alerts on: The frequency of patients monitored with adequate data quality as adequate clinical user satisfaction in the initial versus the last part of the trial (primary outcome).
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Adult participants (≥18 years)
* Patients assessed by the clinical staff as having an acute condition with risk for clinical deterioration and being either at home (with no apparent need for hospitalization), and/or in hospital OR
* Patients at either at home before, in-hospit…
Contacts