Condition: User Experience · Postoperative Complications · Acute Medical Conditions · Sponsor: Christian S. Meyhoff
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.
This description comes directly from the study's public registry record.
Katja K Head of Clinical, MD · 004528781188 · katja.groenbaek@ward247.com
Eske Kvanner Aasvang, MD · Eske.Kvanner.Aasvang.01@regionh.dk
Always discuss trial participation with your own doctor first.
| The Cleveland Clinic Foundation, General Anesthesiology | Cleveland, Ohio, United States | Not Yet Recruiting |
| Universitätsklinikum Hamburg-Eppendorf (UKE), Zentrum für Anästhesiologie und Intensivmedizin, Klinik und Poliklinik für Anästhesiologie | Hamburg, Germany | Completed |
| University Medical Center Groningen, Department of Anesthesiology | Groningen, Netherlands | Recruiting |
| St. Olavs Hospital HF, Klinikk for anestesi og intensivmedisin | Trondheim, Norway | Completed |
| Liverpool University Hospitals NHS Foundation Trust | Liverpool, United Kingdom | Not Yet Recruiting |
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Source record: clinicaltrials.gov/study/NCT06289699