[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Eske Kvanner Aasvang\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":74},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,45],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":5},"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":20,"type":21},100,"ESTIMATED","INTERVENTIONAL",[24],"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.",[27,28],"Postoperative Care","Deterioration, Clinical",[30,31,32],"Vital sign","continuous monitoring","automated alerts","NOT_YET_RECRUITING","2026-06-10",{"date":36,"type":37},"2026-06-16","ACTUAL",{"date":39,"type":21},"2026-05-28",{"date":41,"type":21},"2028-03-31",{"name":43,"class":44},"Eske Kvanner Aasvang","OTHER",{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":52,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":56,"conditions":57,"keywords":61,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":73},"100627639","wireless-assessment-of-respiratory-and-circulatory-distress---europe-100627639","NCT07451249","Wireless Assessment of Respiratory and Circulatory Distress - Europe","WARD-EU","Inclusion Criteria:\n\n* Adults (≥18 years) admitted to hospitals due to medical or surgical conditions with an expected hospital stay of at least two days.\n* Adults discharged from the hospital who are receiving home-based monitoring using WARD-CSS (Phase 2 only).\n* Willingness to participate and provide informed consent.\n\nExclusion Criteria:\n\n* Patients with severe comorbidities (e.g., severe dementia) that preclude continuous monitoring.\n* Patients unwilling or unable to provide informed consent.\n* Patients unable to wear the monitoring equipment.",true,{"count":54,"type":21},1240,[24],"Hospital patient monitoring in Europe is often intermittent, which can delay detection of clinical deterioration during hospitalization and after discharge. The WARD-EU study aims to describe current monitoring practices and to evaluate the feasibility, acceptability, and usability of the WARD-CSS (Wireless Assessment of Respiratory and Circulatory Distress - Clinical Support System), an algorithm-based continuous monitoring system. The study seeks to assess whether WARD-CSS can be integrated into routine hospital and post-discharge care to support earlier detection of patient deterioration and improved patient monitoring.",[58,59,60],"Patient Deterioration","Patient Monitoring","Clinical Deterioration",[62,63,64],"monitoring","Post-discharge monitoring","Clinical deterioration","2026-02-27",{"date":67,"type":37},"2026-03-05",{"date":69,"type":21},"2026-03-16",{"date":71,"type":21},"2028-06-01",{"name":43,"class":44},5,""]