Alert Frequency, Nurse, and Patient Satisfaction With a wCVSM Software Across Health Care Systems and Cultures
Recruiting now
Conditions studied: User Experience, Postoperative Complications, Acute Medical Conditions
In brief
The goal of this prospective, international multi-centre pilot study is to assess the functionality and user experience of a new vital sign monitoring system in 20 patients and 20 nurses in the general ward at each centre. The patients will be monitored with a wireless, continuous vital sign monitoring systems and answer a questionnaire afterwards. They will in addition have vital signs monitored as per standard practice. The nurses will answer a questionnaire after having had the responsibility for a monitored patient for a full shift. The main aims are: To determine the frequency of alerts activated in the app in relation to the alerts that should be activated based on measured data, to explore current practices of in-hospital monitoring by semi-structured interviews to map differences across systems and to test nurse and patient satisfaction.
Key facts
- Study ID
- NCT06289699
- Run by
- Christian S. Meyhoff
- People needed
- 100
- Starts
- 2024-02-26
- Expected to finish
- 2026-12-31
- Last updated by the study team
- 2025-08-12
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adults (≥18 years)
- Expected stay in the hospital ≥2 days
- Admitted for surgery with expected duration of surgery >2 hours or admitted for acute medical condition with at least one of the following vital sign deviations within 24 hours of acute admission, recorded by the staff
- RR > 21 breaths pr minute
- RR < 11 breaths pr minute
- Pulse (P) > 91 beats pr minute
- Pulse (P) < 50 beats pr minute
- SpO2 < 94 % without oxygen supplementation
- Systolic BP < 110 mmHg
- Systolic BP > 220 mmHg
You may not qualify if…
- Participant expected not to cooperate with study procedures.
- Allergy to plaster or silicone.
- Pacemaker or Implantable Cardioverter Defibrillator (ICD) device.
- Inability to give informed consent.
Where it is running
- University Medical Center Groningen, Department of Anesthesiology — Groningen, Netherlands (enrolling)
- The Cleveland Clinic Foundation, General Anesthesiology — Cleveland, Ohio, United States
- Universitätsklinikum Hamburg-Eppendorf (UKE), Zentrum für Anästhesiologie und Intensivmedizin, Klinik und Poliklinik für Anästhesiologie — Hamburg, Germany
- St. Olavs Hospital HF, Klinikk for anestesi og intensivmedisin — Trondheim, Norway
- Liverpool University Hospitals NHS Foundation Trust — Liverpool, United Kingdom
Full record on ClinicalTrials.gov
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