[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100592616":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":31,"centralContacts":35,"locations":44,"responsibleParty":71,"collaborators":74,"id":81,"slug":82,"hasResults":83,"nctId":84,"briefTitle":85,"officialTitle":86,"acronym":87,"eligibilityCriteria":88,"healthyVolunteers":83,"sex":89,"minAge":90,"maxAge":26,"enrollmentInfo":91,"targetDuration":26,"studyType":94,"phases":95,"briefSummary":97,"conditions":98,"keywords":104,"overallStatus":47,"whyStopped":26,"lastUpdateSubmitDate":111,"lastUpdatePostDateStruct":112,"startDateStruct":115,"completionDateStruct":116,"leadSponsor":118,"locationsCount":119},{"fullName":5,"class":6},"Northwestern University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Intervention--Device Array Use","EXPERIMENTAL","Inpatients will wear the ANNE One device array for obtainment of vital sign assessments.",[13],"Device: Device Array Use",{"label":15,"type":16,"description":17,"interventionNames":18},"Control--Routine Vital Sign Obtainment","ACTIVE_COMPARATOR","Inpatients will have vital signs determined by routine practice, using any other standard of care-accepted method or device.",[19],"Device: Routine Vital Sign Measurement",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DEVICE","Device Array Use","Study participants assigned to the intervention study arm will wear a wireless Bluetooth capable vital sign detection array, with one device externally worn on each of their chest, one finger, and one arm, with healthcare providers using an additional oral temperature probe.",[9],null,{"type":22,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Routine Vital Sign Measurement","Study participants randomized to the control arm will have their vital signs obtained by routine means, without use of the wireless vital sign device array.",[15],[32],{"name":33,"affiliation":5,"role":34},"Gregory (Randy) R Smith Jr, MD MS","PRINCIPAL_INVESTIGATOR",[36,40],{"name":33,"role":37,"phone":38,"phoneExt":26,"email":39},"CONTACT","312-926-5893","g.smith@nm.org",{"name":41,"role":37,"phone":42,"phoneExt":26,"email":43},"Jane S Kim, MS MEd","312-926-7272","jane.kim@northwestern.edu",[45,63],{"facility":46,"status":47,"city":48,"state":49,"zip":50,"country":51,"countryCode":52,"cosmosGeoPoint":53,"geoPoint":58,"contacts":59},"Feinberg 16 West, Northwestern Memorial Hospital","RECRUITING","Chicago","Illinois","60611","United States","US",{"type":54,"coordinates":55},"Point",[56,57],-87.65005,41.85003,{"lat":57,"lon":56},[60,62],{"name":61,"role":37,"phone":38,"phoneExt":26,"email":39},"Gregory R Smith Jr, MD MS",{"name":61,"role":34,"phone":26,"phoneExt":26,"email":26},{"facility":64,"status":65,"city":48,"state":49,"zip":50,"country":51,"countryCode":52,"cosmosGeoPoint":66,"geoPoint":68,"contacts":69},"Northwestern Memorial Hospital","NOT_YET_RECRUITING",{"type":54,"coordinates":67},[56,57],{"lat":57,"lon":56},[70],{"name":33,"role":37,"phone":38,"phoneExt":26,"email":39},{"type":34,"investigatorFullName":72,"investigatorTitle":73,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"Gregory Randall Smith Jr","Professor",[75,78],{"name":76,"class":77},"University of Minnesota Medical School\u002FUniversity of Minnesota Foundation","UNKNOWN",{"name":79,"class":80},"Sibel Health Inc.","INDUSTRY","100592616","effect-of-anne-one-wellue-device-array-use-on-staff-bedside-vital-sign-measurement-activity-100592616",false,"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.","ALL","18 Years",{"count":92,"type":93},270,"ESTIMATED","INTERVENTIONAL",[96],"NA","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.",[99,100,101,102,103],"Vital Sign Evaluation","Vital Sign Monitoring","Sleep Quality","Provider Behavior","Patient Satisfaction",[105,106,107,108,109,110],"time motion study","vital signs","sleep quality","inpatient sleep","wireless device","patient satisfaction","2025-06-02",{"date":113,"type":114},"2025-06-05","ACTUAL",{"date":111,"type":114},{"date":117,"type":93},"2026-07-31",{"name":5,"class":6},2]