[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100648892":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":24,"centralContacts":28,"locations":18,"responsibleParty":34,"collaborators":18,"id":35,"slug":36,"hasResults":37,"nctId":38,"briefTitle":39,"officialTitle":40,"acronym":41,"eligibilityCriteria":42,"healthyVolunteers":37,"sex":43,"minAge":44,"maxAge":18,"enrollmentInfo":45,"targetDuration":18,"studyType":48,"phases":49,"briefSummary":51,"conditions":52,"keywords":54,"overallStatus":62,"whyStopped":18,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":18},{"fullName":5,"class":6},"University of Colorado, Denver","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Alarms ON","EXPERIMENTAL","A soft buzz and blinking light emitted from the incentive spirometer base attachment (monitor) will go off every twenty minutes during waking hours after major surgery.",[13],"Device: Alarms ON",{"label":15,"type":16,"description":17,"interventionNames":18},"Alarms OFF","NO_INTERVENTION","The patient will be given an incentive spirometer with the base attachment (monitor). No light or soft buzz will be emitted from the device.",null,[20],{"type":21,"name":9,"description":22,"armGroupLabels":23,"otherNames":18},"DEVICE","Alarms are turned ON. The alarms include a dim light and soft buzz every twenty minutes during waking hours.",[9],[25],{"name":26,"affiliation":5,"role":27},"Ana Fernandez-Bustamante, MD, PhD","PRINCIPAL_INVESTIGATOR",[29],{"name":30,"role":31,"phone":32,"phoneExt":18,"email":33},"Emily G Helmer, BA","CONTACT","(303) 724-2938","emily.helmer@cuanschutz.edu",{"type":27,"investigatorFullName":26,"investigatorTitle":26,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"100648892","reminder-enhanced-incentive-spirometry-evaluation-100648892",false,"NCT07728214","Reminder-enhanced Incentive Spirometry Evaluation","Reminder-enhanced Incentive Spirometry Evaluation (RISE)","RISE","Inclusion Criteria:\n\n* ≥18 years\n* Planned non-cardiac surgery under general anesthesia with at least one night of hospitalization expected\n* Preoperative ARISCAT risk score ≥26\n* Signed informed consent\n\nExclusion Criteria:\n\n* Inability to perform IS due to refusal, cognitive impairment, neuromuscular weakness, anatomical, or any other reasons (e.g., tracheotomy, oral surgery, unable to hold incentive spirometer)\n* Have a severe hearing or visual acuity impairment that prevents them from hearing or seeing the audible and visual IS reminders\n* Are part of a vulnerable population (minors, pregnant, prisoners)\n* Lack of informed consent","ALL","18 Years",{"count":46,"type":47},88,"ESTIMATED","INTERVENTIONAL",[50],"NA","The purpose of this study is to test whether automatic reminders with a light and a soft sound help patients improve deep breathing exercises after surgery. These breathing exercises are routinely done with the help of a plastic device that you attach to your mouth and you take a deep breath. These exercises are routinely recommended after major surgery to improve the oxygen level in your blood and reduce other respiratory problems.",[53],"Hypoxemia",[55,56,57,58,59,60,53,61],"Incentive Spirometry","IS","Spirometer","InSee Device","Postoperative Pulmonary Complications","Hypoxia","Breathing Exercises","NOT_YET_RECRUITING","2026-07-22",{"date":65,"type":66},"2026-07-27","ACTUAL",{"date":68,"type":47},"2026-11-01",{"date":70,"type":47},"2029-01-01",{"name":5,"class":6}]