[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100616318":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":29,"centralContacts":33,"locations":39,"responsibleParty":57,"collaborators":24,"id":59,"slug":60,"hasResults":61,"nctId":62,"briefTitle":63,"officialTitle":64,"acronym":24,"eligibilityCriteria":65,"healthyVolunteers":61,"sex":66,"minAge":67,"maxAge":68,"enrollmentInfo":69,"targetDuration":24,"studyType":72,"phases":73,"briefSummary":75,"conditions":76,"keywords":78,"overallStatus":41,"whyStopped":24,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":94},{"fullName":5,"class":6},"University of Michigan","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"PICTURE-Pediatric scores and alerts","EXPERIMENTAL","This arm will happen for two four-week periods.",[13],"Device: PICTURE-Pediatric scores and alerts",{"label":15,"type":6,"description":16,"interventionNames":17},"Control Arm","During the control arm, the PICTURE scores and alerts will not be shown. This arm will happen for two four-week periods.",[18],"Other: Control Arm - Scores and alerts hidden",[20,25],{"type":21,"name":9,"description":22,"armGroupLabels":23,"otherNames":24},"DEVICE","Patients that satisfy the inclusion criteria will receive PICTURE-Pediatric scores and alerts. Scores are numbers that indicate the likelihood that the patient may experience deterioration in the next 24 hours, i.e., the higher the score, the higher the likelihood of deterioration. Alerts will be sent through pages or phone notifications, depending on the user's current method of receiving non-routine communications. Scores are also available through electronic medical record as a column that can be wrenched into the patient lists, in a patient summary report and as a vital and\u002For a flowsheet. The scores for patients with an alert (scores that have surpassed the corresponding alert thresholds) will be colored accordingly (yellow or red) in the electronic medical record. Various staff on the clinical team will use this data to help determine intervention and or escalation depending on the alerts.",[9],null,{"type":6,"name":26,"description":27,"armGroupLabels":28,"otherNames":24},"Control Arm - Scores and alerts hidden","The morning rounds and prerounding procedures will revert back to the baseline procedures before the trial. All care teams will be notified about this transition in advance and will be directed to revert back to the standard of care.",[15],[30],{"name":31,"affiliation":5,"role":32},"Rodney Daniels","PRINCIPAL_INVESTIGATOR",[34],{"name":35,"role":36,"phone":37,"phoneExt":24,"email":38},"Jay Semerad","CONTACT","734-647-4751","jsemerad@umich.edu",[40],{"facility":5,"status":41,"city":42,"state":43,"zip":44,"country":45,"countryCode":46,"cosmosGeoPoint":47,"geoPoint":52,"contacts":53},"RECRUITING","Ann Arbor","Michigan","48109","United States","US",{"type":48,"coordinates":49},"Point",[50,51],-83.74088,42.27756,{"lat":51,"lon":50},[54,55],{"name":35,"role":36,"phone":37,"phoneExt":24,"email":38},{"name":56,"role":32,"phone":24,"phoneExt":24,"email":24},"Rodney Daniels, MD, FAAP",{"type":32,"investigatorFullName":31,"investigatorTitle":58,"investigatorAffiliation":5,"oldNameTitle":24,"oldOrganization":24},"Clinical Associate Professor","100616318","predicting-icu-transfers-and-other-unforeseen-events-picture-pediatric-100616318",false,"NCT07304050","Predicting ICU Transfers and Other Unforeseen Events (PICTURE)-Pediatric","Pilot Randomized Controlled Trial of PICTURE-Pediatric","Inclusion Criteria - Patients:\n\n* Age ≥30 days and ≤25 years\n* Be on the general care wards of Mott Children's Hospital or boarding in the Emergency Department (ED), but admitted to a pediatric floor medical team. These will be enforced by these criteria:\n\n  1. Patient class: not emergency b. Patient level of care: not Intensive Care unit (ICU) c. Patient locations (per protocol)\n\n     Exclusion Criteria - Patients:\n* Patients that do not meet the inclusion criteria","ALL","30 Days","25 Years",{"count":70,"type":71},375,"ESTIMATED","INTERVENTIONAL",[74],"NA","The purpose of this study is to evaluate the effectiveness and user satisfaction of the study teams early warning system, called PICTURE, which utilizes artificial intelligence (AI) techniques and algorithms to identify patient deterioration on pediatric units within Mott Children's Hospital.\n\nIn this pilot study the patient care team will review the PICTURE information and alerts. Morning rounds will be partially informed by the PICTURE scores and the scores will be included in the hand off notes for the patients with a red score.\n\nThe primary purpose of this study is to test the hypothesis that the combination of the PICTURE-Pediatric model, the proposed workflow and the proposed interface results in at least 80% compliance.\n\nNo participants will be consented as the Institutional review board has approved a waiver of consent for THE clinicians and the patients information being reviewed.\n\nThe enrollment numbers will include only the clinicians.",[77],"Clinical Deterioration",[79,80,81,82,83,84],"Artificial Intelligence model","Usability","Acceptability","Questionnaire","Real-time alerts","Workflow compliance","2026-03-03",{"date":87,"type":88},"2026-03-05","ACTUAL",{"date":90,"type":88},"2026-02-09",{"date":92,"type":71},"2027-01",{"name":5,"class":6},1]