[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"vital-sign-monitoring\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:vital-sign-monitoring":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,40,79,111],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":4},"100642598","neonatal-wireless-transmission-system-hospital-adoption-and-planning-for-implementation-study-100642598",false,"NCT07650045","Neonatal Wireless Transmission System: Hospital Adoption and Planning for Implementation Study","NEWTS HAPI-1","Inclusion Criteria:\n\n* staff with experience of working or supporting NICU care Informed consent\n\nExclusion Criteria:\n\n* no informed consent",true,"ALL","18 Years","65 Years",{"count":21,"type":22},50,"ESTIMATED","OBSERVATIONAL","To explore the feasibility, acceptability, and implementation considerations associated with the adoption of the NeWTS system within NHS neonatal services.",[26,27],"Preterm Infants","Vital Sign Monitoring","NOT_YET_RECRUITING","2026-06-11",{"date":31,"type":32},"2026-06-16","ACTUAL",{"date":34,"type":22},"2026-07-01",{"date":36,"type":22},"2026-12-31",{"name":38,"class":39},"Cambridge University Hospitals NHS Foundation Trust","OTHER",{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":46,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":17,"minAge":48,"maxAge":4,"enrollmentInfo":49,"targetDuration":4,"studyType":51,"phases":52,"briefSummary":54,"conditions":55,"keywords":60,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":76,"locationsCount":78},"100622551","continuous-vital-sign-monitoring-versus-routine-spot-checks-in-patients-after-non-cardiac-surgery-100622551","NCT07385092","Continuous Vital Sign Monitoring Versus Routine Spot-checks in Patients After Non-cardiac Surgery","The Effect of Continuous Monitoring Versus Routine Spot-checks on Altered Vital Signs in Patients Recovering From Non-cardiac Surgery on Normal Wards: the \"COME ON, NOW!\" Trial","COME ON NOW","Inclusion Criteria:\n\nConsenting patients ≥45 years scheduled for elective non-cardiac (abdominal and thoracic) surgery with planned postoperative admission to a normal ward after an overnight stay in an advanced post-anesthesia care unit.\n\nExclusion Criteria:\n\n* Emergency surgery\n* Pregnancy\n* Impossibility to perform continuous monitoring with the Radius VSM sensor (Masimo, Irvine, CA)\n* Atrial fibrillation\n* Patients designated Do Not Resuscitate, or are receiving end-of-life care","45 Years",{"count":50,"type":22},264,"INTERVENTIONAL",[53],"NA","The \"COME ON, NOW!\" trial is a randomized, single-center trial in patients recovering from non-cardiac surgery on normal wards investigating whether continuous vital sign monitoring - compared to routine spot-checks by nurses - reduces the total duration of abnormal vital signs per hour during the first 48 hours after admission to the normal ward.",[27,56,57,58,59],"Post Operative Complications","Non-cardiac Surgery","RCT","Anesthesiology",[61,62,63,64,65,66,67,68],"continuous vital signs","vital signs","vital sign monitoring","post-operative care","anesthesiology","anesthesia","hypotension","post-operative complications","RECRUITING","2026-02-27",{"date":72,"type":32},"2026-03-02",{"date":74,"type":32},"2026-02-24",{"date":36,"type":22},{"name":77,"class":39},"Universitätsklinikum Hamburg-Eppendorf",1,{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":85,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":87,"targetDuration":4,"studyType":51,"phases":89,"briefSummary":90,"conditions":91,"keywords":96,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":102,"lastUpdatePostDateStruct":103,"startDateStruct":105,"completionDateStruct":106,"leadSponsor":108,"locationsCount":110},"100592616","effect-of-anne-one-wellue-device-array-use-on-staff-bedside-vital-sign-measurement-activity-100592616","NCT06995742","Effect of ANNE One-Wellue Device Array Use on Staff Bedside Vital Sign Measurement Activity","Effect of ANNE One-Wellue Device Array Use on Staff Bedside Vital Sign Measurement Activity: A Randomized Controlled Trial","ANNE One TMRCT","Inclusion Criteria:\n\n* Inpatients admitted to Northwestern Memorial Hospital, Feinberg Unit 16 West.\n\nExclusion Criteria:\n\n* Primary language other than English, under isolation status, pregnant patients, prisoners, employees or students of the hospital or Northwestern University.",{"count":88,"type":22},270,[53],"Randomized controlled trial of a time motion study of time spent obtaining and charting vital signs for inpatients, comparing use of a wireless Bluetooth vital sign array as intervention versus routine vital sign obtainment activity on a general medical floor.",[92,27,93,94,95],"Vital Sign Evaluation","Sleep Quality","Provider Behavior","Patient Satisfaction",[97,62,98,99,100,101],"time motion study","sleep quality","inpatient sleep","wireless device","patient satisfaction","2025-06-02",{"date":104,"type":32},"2025-06-05",{"date":102,"type":32},{"date":107,"type":22},"2026-07-31",{"name":109,"class":39},"Northwestern University",2,{"id":112,"slug":113,"hasResults":11,"nctId":114,"briefTitle":115,"officialTitle":116,"acronym":4,"eligibilityCriteria":117,"healthyVolunteers":11,"sex":17,"minAge":118,"maxAge":18,"enrollmentInfo":119,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":121,"conditions":122,"keywords":124,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":129,"lastUpdatePostDateStruct":130,"startDateStruct":132,"completionDateStruct":134,"leadSponsor":136,"locationsCount":78},"100580411","the-effect-of-two-different-bathing-methods-on-vital-signs-and-comfort-in-picubath-trial-100580411","NCT06836947","The Effect of Two Different Bathing Methods on Vital Signs and Comfort in PICU:Bath Trial","The Effect of Two Different Bathing Methods on Vital Signs and Comfort in Pediatric Intensive Care Unit:Bath Trial","Inclusion Criteria:\n\n1. Being hospitalized in Behçet Uz Pediatric Intensive Care Unit\n2. No contraindications to bathing\n3. Parent's willingness to participate in the study\n\nExclusion Criteria:\n\n1. Having a contraindication to bathing\n2. Parents were not willing to participate in the study","28 Days",{"count":120,"type":22},52,"The study was planned to be conducted and completed within 6 months after ethics committee approval was obtained. The study is a prospective, quasi-experimental study.\n\nThe population of the study will consist of children who are hospitalized in the Pediatric Intensive Care Unit of SBÜ. İzmir Dr. Behçet Uz Pediatric Diseases and Surgery Training and Research Hospital. The vital signs and comfort of the children of the parents who agreed to participate in the study will be measured before bathing (baseline) and care will be taken to ensure that they are similar in both groups.\n\nChildren in the study will not be randomized. In the routine operation of the clinic, traditional bathing is performed once a week and wipe bathing is performed once every two days. Wipe bathing is performed at 36-37 degrees water with 10 ml of chlorhexidine in 200 ml of water. Traditional bathing is also performed with 36-37 degrees water in bed or in the bathtub. In the study, no intervention will be performed and the outcomes will be measured and compared with each other before and after both bathing procedures.\n\nPhysiologic parameters including respiratory rate, pulse rate, oxygen saturation and comfort levels of newborns just before, during and after the bathing process (1st and 5th minute) will be evaluated and compared with each other. To avoid bias in the study, all bathing procedures will be performed by Specialist Nurse Esat Erdem GÖKPINAR.\n\nTranslated with DeepL.com (free version)",[27,123],"Comfort",[125,126,127,62,128],"pediatrics","bath","nursing care","comfort","2025-05-05",{"date":131,"type":32},"2025-05-07",{"date":133,"type":32},"2025-04-09",{"date":135,"type":22},"2025-05-30",{"name":137,"class":39},"Izmir Katip Celebi University"]