[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Christian S. Meyhoff\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":43},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":21,"conditions":22,"keywords":26,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100538351",false,"NCT06289699","Alert Frequency, Nurse, and Patient Satisfaction With a wCVSM Software Across Health Care Systems and Cultures","Alert Frequency, Nurse, and Patient Satisfaction With a Continuous Wireless Vital Sign Monitoring Software Across Health Care Systems and Cultures","Inclusion Criteria:\n\n* Adults (≥18 years)\n* Expected stay in the hospital ≥2 days\n* 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\n\n  * RR \\> 21 breaths pr minute\n  * RR \\\u003C 11 breaths pr minute\n  * Pulse (P) \\> 91 beats pr minute\n  * Pulse (P) \\\u003C 50 beats pr minute\n  * SpO2 \\\u003C 94 % without oxygen supplementation\n  * Systolic BP \\\u003C 110 mmHg\n  * Systolic BP \\> 220 mmHg\n\nExclusion Criteria:\n\n* Participant expected not to cooperate with study procedures.\n* Allergy to plaster or silicone.\n* Pacemaker or Implantable Cardioverter Defibrillator (ICD) device.\n* Inability to give informed consent.","ALL","18 Years",{"count":18,"type":19},100,"ESTIMATED","OBSERVATIONAL","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.",[23,24,25],"User Experience","Postoperative Complications","Acute Medical Conditions",[27,28,29,23,24,25],"continuous wireless vital sign monitoring","vital sign deviation","healthcare system and culture","RECRUITING","2025-08-11",{"date":33,"type":34},"2025-08-12","ACTUAL",{"date":36,"type":34},"2024-02-26",{"date":38,"type":19},"2026-12-31",{"name":40,"class":41},"Christian S. Meyhoff","OTHER",5,""]