[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100641971":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":11,"centralContacts":20,"locations":30,"responsibleParty":49,"collaborators":53,"id":57,"slug":58,"hasResults":59,"nctId":60,"briefTitle":61,"officialTitle":62,"acronym":63,"eligibilityCriteria":64,"healthyVolunteers":59,"sex":65,"minAge":66,"maxAge":11,"enrollmentInfo":67,"targetDuration":11,"studyType":70,"phases":71,"briefSummary":73,"conditions":74,"keywords":77,"overallStatus":81,"whyStopped":11,"lastUpdateSubmitDate":82,"lastUpdatePostDateStruct":83,"startDateStruct":86,"completionDateStruct":88,"leadSponsor":90,"locationsCount":91},{"fullName":5,"class":6},"Rigshospitalet, Denmark","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Adult, hospitalized patients who are monitored for vital signs in the general wards","EXPERIMENTAL",null,[13],"Device: Continuous vital sign monitoring",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":11},"DEVICE","Continuous vital sign monitoring","The intervention involves continuous, real-time vital sign monitoring using sensors to measure vital signs combined with WARD-CSS and novel algorithms designed to detect clinically relevant deviations in the vital signs.",[9],[21,26],{"name":22,"role":23,"phone":24,"phoneExt":11,"email":25},"Aslak B Johansen, M.D.","CONTACT","+4522952551","aslak.broby.johansen@regionh.dk",{"name":27,"role":23,"phone":28,"phoneExt":11,"email":29},"Eske K Aasvang, DMSci","+4526232076","Eske.Kvanner.Aasvang.01@regionh.dk",[31,43],{"facility":32,"status":11,"city":33,"state":11,"zip":34,"country":35,"countryCode":36,"cosmosGeoPoint":37,"geoPoint":42,"contacts":11},"Rigshospitalet","Copenhagen","2100","Denmark","DK",{"type":38,"coordinates":39},"Point",[40,41],12.56553,55.67594,{"lat":41,"lon":40},{"facility":44,"status":11,"city":33,"state":11,"zip":45,"country":35,"countryCode":36,"cosmosGeoPoint":46,"geoPoint":48,"contacts":11},"Bispebjerg Hospital","2400",{"type":38,"coordinates":47},[40,41],{"lat":41,"lon":40},{"type":50,"investigatorFullName":51,"investigatorTitle":52,"investigatorAffiliation":5,"oldNameTitle":11,"oldOrganization":11},"SPONSOR_INVESTIGATOR","Eske Kvanner Aasvang","Professor, M.D., DMSCi",[54,55],{"name":5,"class":6},{"name":56,"class":6},"University Hospital Bispebjerg and Frederiksberg","100641971","optimized-novel-wireless-assessment-of-respiratory-and-circulatory-dirstress---alarm-validation-100641971",false,"NCT07649642","Optimized Novel Wireless Assessment of Respiratory and Circulatory Dirstress - Alarm Validation","Validation of the Accuracy and Relevance of Continuous Vital Sign Monitoring Using an AI-algorithm in Hospitalized Patients","ONWARD - AV","Inclusion criteria:\n\nPatients can be included if they meet all the following criteria:\n\n* Age ≥ 18 years\n* Patients assessed by the clinical staff as having an acute condition with risk for clinical deterioration.\n* Expected admission for more than 24 hours to a general ward.\n\nExclusion criteria:\n\nPatients are excluded if they meet any of the following criteria:\n\n* Having implanted electronic devices (such as pacemaker or Implantable Cardioverter Defibrillator (ICD) device).\n* Known pregnancy or breastfeeding\n* Inability to give informed consent.\n* The participant expected not to cooperate with study procedures.","ALL","18 Years",{"count":68,"type":69},100,"ESTIMATED","INTERVENTIONAL",[72],"NA","The ONWARD study evaluates user experiences from continuous vital sign monitoring alarms sent to the clinical staff in case of deviating vital signs at the general hospital ward. User experiences are evaluated though a 5-point likert questionnaire.",[75,76],"Postoperative Care","Deterioration, Clinical",[78,79,80],"Vital sign","continuous monitoring","automated alerts","NOT_YET_RECRUITING","2026-06-10",{"date":84,"type":85},"2026-06-16","ACTUAL",{"date":87,"type":69},"2026-05-28",{"date":89,"type":69},"2028-03-31",{"name":51,"class":6},2]