Actively Recruiting
Alert Frequency, Nurse, and Patient Satisfaction With a wCVSM Software Across Health Care Systems and Cultures
Led by Christian S. Meyhoff · Updated on 2025-08-12
100
Participants Needed
5
Research Sites
148 weeks
Total Duration
On this page
Sponsors
C
Christian S. Meyhoff
Lead Sponsor
R
Rigshospitalet, Denmark
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Alert Frequency, Nurse, and Patient Satisfaction With a wCVSM Software Across Health Care Systems and Cultures
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults (≥18 years)
- Expected hospital stay of 2 days or more
- Admitted for surgery with expected duration over 2 hours or admitted for acute medical condition with at least one vital sign deviation within 24 hours:
- Respiratory rate > 21 breaths per minute
- Respiratory rate < 11 breaths per minute
- Pulse > 91 beats per minute
- Pulse < 50 beats per minute
- Oxygen saturation < 94% without oxygen supplementation
- Systolic blood pressure < 110 mmHg
- Systolic blood pressure > 220 mmHg
You will not qualify if you...
- Expected inability to cooperate with study procedures
- Allergy to plaster or silicone
- Presence of pacemaker or implantable cardioverter defibrillator (ICD) device
- Inability to provide informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 5 locations
1
The Cleveland Clinic Foundation, General Anesthesiology
Cleveland, Ohio, United States, 44195
Not Yet Recruiting
2
Universitätsklinikum Hamburg-Eppendorf (UKE), Zentrum für Anästhesiologie und Intensivmedizin, Klinik und Poliklinik für Anästhesiologie
Hamburg, Germany, 20246
Completed
3
University Medical Center Groningen, Department of Anesthesiology
Groningen, Netherlands, 9700
Actively Recruiting
4
St. Olavs Hospital HF, Klinikk for anestesi og intensivmedisin
Trondheim, Norway, 7006
Completed
5
Liverpool University Hospitals NHS Foundation Trust
Liverpool, United Kingdom, L7 8YE
Not Yet Recruiting
Research Team
K
Katja K Head of Clinical, MD
CONTACT
E
Eske Kvanner Aasvang, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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