[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"clinical-deterioration\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:clinical-deterioration":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,48,78],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"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":20,"type":21},375,"ESTIMATED","INTERVENTIONAL",[24],"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.",[27],"Clinical Deterioration",[29,30,31,32,33,34],"Artificial Intelligence model","Usability","Acceptability","Questionnaire","Real-time alerts","Workflow compliance","RECRUITING","2026-03-03",{"date":38,"type":39},"2026-03-05","ACTUAL",{"date":41,"type":39},"2026-02-09",{"date":43,"type":21},"2027-01",{"name":45,"class":46},"University of Michigan","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":55,"sex":16,"minAge":56,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":60,"conditions":61,"keywords":64,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":77},"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,"18 Years",{"count":58,"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.",[62,63,27],"Patient Deterioration","Patient Monitoring",[65,66,67],"monitoring","Post-discharge monitoring","Clinical deterioration","NOT_YET_RECRUITING","2026-02-27",{"date":38,"type":39},{"date":72,"type":21},"2026-03-16",{"date":74,"type":21},"2028-06-01",{"name":76,"class":46},"Eske Kvanner Aasvang",5,{"id":79,"slug":80,"hasResults":11,"nctId":81,"briefTitle":82,"officialTitle":83,"acronym":84,"eligibilityCriteria":85,"healthyVolunteers":55,"sex":16,"minAge":86,"maxAge":4,"enrollmentInfo":87,"targetDuration":4,"studyType":22,"phases":89,"briefSummary":90,"conditions":91,"keywords":92,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":106},"100564820","prevention-of-functional-and-cognitive-impairment-through-a-multicomponent-exercise-program-in-hospitalized-older-adults-100564820","NCT06634147","Prevention of Functional and Cognitive Impairment Through a Multicomponent Exercise Program in Hospitalized Older Adults","Prevention of Functional and Cognitive Impairment Through a Multicomponent Exercise Program in Hospitalized Older Adults (Geriatrics and Internal Medicine): a Randomized Clinical Trial. Multicenter Study (HUN, CHU-T, ULSBM, and HNSM)","PREDISC","Inclusion Criteria:\n\n* Age equal to or greater than 75 years, admitted to the acute care unit for medical conditions.\n\nExclusion Criteria:\n\n* Explicit refusal expressed verbally or refusal to sign the informed consent by the patient\u002Fmain caregiver\u002Flegal guardian or inability to obtain it.\n* Life expectancy of less than 3 months or terminal oncological or non-oncological disease.\n* Inability to follow up.\n* Inability to participate in a multicomponent exercise program.\n* Medical contraindication to exercise.\n* Major neurocognitive disorder at moderate to severe stage (GDS - Fast Reisberg 5-7).\n* Moderate to severe disability (measured by the Barthel Index (BI \\<60)).\n* Expected hospital stay of less than 6 days.","75 Years",{"count":88,"type":21},296,[24],"The goal of this clinical trial is to determine whether a multicomponent exercise program improves functional capacity and cognitive status in hospitalized elderly patients aged 75 and older. Additionally, the study aims to assess the impact of this program on medication use, quality of life, and overall health outcomes. Key questions include whether the program enhances functional and cognitive capacities and which subgroups benefit most, such as frail patients or those with cognitive impairment.\n\nParticipants will engage in a structured exercise program that includes strength training, balance exercises, and walking, all designed to improve mobility and reduce fall risk. They will attend supervised sessions several times a week, allowing for individualized attention and adjustments based on their abilities and health status.\n\nThroughout the study, changes in functional capacity will be monitored using standardized assessments that measure mobility, strength, and overall physical functioning. Cognitive assessments will evaluate any changes in cognitive status during the intervention and follow-up periods post-discharge. Participants will provide information on medication usage to analyze whether the exercise program can reduce the need for medications or help manage common polypharmacy issues.\n\nSurveys and interviews will assess participants' quality of life, including physical, emotional, and social well-being, before and after the intervention. Follow-up assessments will track progress and outcomes, ensuring long-term benefits of the exercise program are documented.\n\nThe study will include a diverse sample from multiple centers, focusing on individuals aged over 75 who are hospitalized in Geriatrics and Internal Medicine services across participating centers (HUN, CHU-T, ULSBM, and HNSM). Exclusion criteria will ensure safety, excluding those with terminal illnesses or significant contraindications for exercise.\n\nThis clinical trial aims to recruit 296 patients, providing valuable insights into the benefits of physical activity for elderly patients during hospitalization and informing future care practices.",[27],[93,94,95,96],"hospital acquired disability","exercise","function","cognition","2025-07-15",{"date":99,"type":39},"2025-07-18",{"date":101,"type":39},"2025-02-01",{"date":103,"type":21},"2026-12-01",{"name":105,"class":46},"Fundacion Miguel Servet",2]