[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"acute-hospitalization\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:acute-hospitalization":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,59,90],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":37,"overallStatus":46,"whyStopped":4,"lastUpdateSubmitDate":47,"lastUpdatePostDateStruct":48,"startDateStruct":51,"completionDateStruct":53,"leadSponsor":55,"locationsCount":58},"100566450","efficiency-of-the-medidux-smartphone-app-for-demission-management-in-patients-medicated-in-acute-admission-unit-aau-100566450",false,"NCT06655337","Efficiency of the \"Medidux\" Smartphone App for Demission Management in Patients Medicated in Acute Admission Unit (AAU)","Efficiency of the \"Medidux\" Smartphone App for Demission Management in Patients Medicated in Acute Admission Unit (AAU): a Randomized Controlled Trial.","EffiDux","Inclusion Criteria:\n\n* Signed Informed Consent Form (ICF)\n* Age ≥ 18 years\n* (Self-)admission to the involved Acute Admissions Unit (AAU)\n* \"Lead symptom\" identified as coughing, back pain or abdominal discomfort\n* Participant within ESI triage system group 4 (standard) and 5 (non-urgent)\n* German-speaking\n* Ownership of a smartphone or other mobile device with iOS or Android operating system\n\nExclusion Criteria:\n\n* Age \\\u003C 18 years\n* Participant whose compliance to the study's protocol, e.g. due to mental health problems, physical problems, or the private life situation, can be justifiably doubted\n* Participant with insufficient knowledge about the use of a smartphone or other mobile device with iOS or Android operating system\n* Participant already using or planning to use another comparable electronic patient-reported symptom monitoring system (e.g. CANKADO) during this trial","ALL","18 Years",{"count":20,"type":21},417,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical trial is to evaluate whether the use of the medidux™ smartphone app can optimize post-discharge management for patients admitted to Acute Admission Units (AAU) with non-urgent health complaints. This trial includes adult patients (age ≥ 18) in Emergency Severity Index (ESI) triage system groups 4 (standard) or 5 (non-urgent), presenting with primary symptoms such as cough, back pain, or abdominal discomfort.\n\nThe main question it aims to answer is:\n\nCan the medidux™ app reduce the incidence of AAU readmissions, emergency hospitalizations, or consultations with other medical providers within 7 days after initial admission?\n\nResearchers will compare participants using the medidux™ app (intervention arm) with those receiving standard care (control arm) to observe potential differences in the rates of readmissions, emergency hospitalizations, and medical consultations.\n\nParticipants will:\n\n* use the medidux™ app to monitor their symptoms and vital parameters for 7 days after discharge (intervention arm).\n* receive follow-up consultations at day 7 and at day 28 to assess symptom progression and any healthcare interactions (both arms).",[27,28,29,30,31,32,33,34,35,36],"Acute Disease","Acute Hospitalization","Coughing","Back Pain","Abdominal Pain (AP)","Patient Discharge","Patient Readmission","Mobile Health Apps","Mobile Health Technology (mHealth)","Patient Reported Outcome (PRO)",[27,32,33,29,30,38,39,40,41,42,43,44,45],"Abdominal Pain","Mobile Health Applications","Remote Monitoring","Post-discharge Care","Symptom Monitoring","Health Behaviour","Telemedicine","Randomized Controlled Trial","RECRUITING","2025-09-29",{"date":49,"type":50},"2025-10-03","ACTUAL",{"date":52,"type":50},"2025-09-28",{"date":54,"type":21},"2027-03-28",{"name":56,"class":57},"Mobile Health AG","INDUSTRY",1,{"id":60,"slug":61,"hasResults":11,"nctId":62,"briefTitle":63,"officialTitle":64,"acronym":65,"eligibilityCriteria":66,"healthyVolunteers":11,"sex":17,"minAge":67,"maxAge":4,"enrollmentInfo":68,"targetDuration":4,"studyType":22,"phases":70,"briefSummary":71,"conditions":72,"keywords":73,"overallStatus":79,"whyStopped":4,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":4},"100607029","hospital-to-home-rehabilitation-through-exercise-and-cognitive-training-100607029","NCT07183241","Hospital-to-Home Rehabilitation Through Exercise and Cognitive Training","Comparación Entre Ingreso Hospitalario y Hospitalización Domiciliaria y Análisis de Una Intervención Multicomponente en Adultos Mayores: Ensayo Clínico Aleatorizado","H-REACT","Inclusion Criteria:\n\n* Older adults admitted to the hospital or Hospital at Home (HaH) due to an acute illness.\n* Residents of Navarre.\n* Willingness to participate on a voluntary basis.\n* Ability to ambulate with or without assistance.\n* Ability to communicate and collaborate with the research staff.\n\nExclusion Criteria:\n\n* Acute illness that does not allow the assessment and practice of physical exercise during the study.\n* Medical contraindication for the practice of physical exercise.\n* Severe dementia.\n* Refusal to sign the informed consent form by the patient, accompanying person, or legal guardian.","65 Years",{"count":69,"type":21},200,[24],"This research project is structured in two phases: an initial observational phase and a subsequent randomized controlled trial (RCT) phase. The goal of the observational phase is to compare hospital admission and Hospital at Home (HaH). The objective of the RCT is to assess the effectiveness of a multicomponent intervention following acute hospitalization in older adults. The main questions it aims to answer are:\n\n* What are the differences between hospital admission and HaH in sedentary and physical activity levels?\n* What are the effects of a multicomponent intervention following acute hospitalization in older adults?\n\nResearchers will compare a post-discharge multicomponent intervention to usual care to see the effects on physical and cognitive function.\n\nParticipants will receive a home-based cognitive and physical exercise intervention or usual care.",[28],[74,75,76,77,78],"acute hospitalization","older adults","exercise","hospital at home","cognitive","NOT_YET_RECRUITING","2025-09-17",{"date":82,"type":50},"2025-09-19",{"date":84,"type":21},"2025-10",{"date":86,"type":21},"2027-06",{"name":88,"class":89},"Universidad Pública de Navarra","OTHER",{"id":91,"slug":92,"hasResults":11,"nctId":93,"briefTitle":94,"officialTitle":95,"acronym":96,"eligibilityCriteria":97,"healthyVolunteers":11,"sex":17,"minAge":67,"maxAge":4,"enrollmentInfo":98,"targetDuration":4,"studyType":100,"phases":4,"briefSummary":101,"conditions":102,"keywords":106,"overallStatus":46,"whyStopped":4,"lastUpdateSubmitDate":111,"lastUpdatePostDateStruct":112,"startDateStruct":114,"completionDateStruct":116,"leadSponsor":118,"locationsCount":58},"100585551","discharge-recommendations-for-older-adults-using-physical-outcome-measure-100585551","NCT06903832","Discharge Recommendations for Older Adults Using Physical Outcome Measure","Discharge Recommendations for Older Adults Using Physical Outcome Measure (DROP)","DROP","Inclusion Criteria:\n\n* Aged 65 years and older\n* Able to ambulate without physical assistance with or without walking aids as per premorbid status for at least 5 metres\n* Clinical Frailty Scale (CFS) of ≤ 5\n* Able to follow instructions (Abbreviated Mental Test (AMT) ≥ 5)\n\nExclusion Criteria:\n\n* Admitted for acute orthopaedic or neurological conditions with physical deficits that affect functional mobility\n* Requires physical assistance for functional mobility from ≥ 1 person\n* Clinical Frailty Scale (CFS) of \\> 5\n* AMT \\\u003C 5 (Lack capacity to consent to study)",{"count":99,"type":21},60,"OBSERVATIONAL","The aim of this study is to explore if the use of Sit to Stand Test and Gait speed Test could assist physiotherapist with discharge planning decisions for older adults who are admitted to an acute hospital.",[103,104,28,105],"Discharge Planning","Older Adults (65 Years and Older)","OUTCOME MEASURES",[107,28,108,75,109,110],"Discharge planning","Physical outcome measure","Gait Speed Test","Five Times Sit to Stand Test","2025-04-29",{"date":113,"type":50},"2025-04-30",{"date":115,"type":50},"2025-04-01",{"date":117,"type":21},"2026-09-30",{"name":119,"class":89},"National University Hospital, Singapore"]