[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100561988":3},{"organization":4,"armGroups":7,"interventions":13,"overallOfficials":18,"centralContacts":32,"locations":38,"responsibleParty":57,"collaborators":60,"id":68,"slug":69,"hasResults":70,"nctId":71,"briefTitle":72,"officialTitle":72,"acronym":73,"eligibilityCriteria":74,"healthyVolunteers":70,"sex":75,"minAge":76,"maxAge":10,"enrollmentInfo":77,"targetDuration":10,"studyType":80,"phases":10,"briefSummary":81,"conditions":82,"keywords":10,"overallStatus":41,"whyStopped":10,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":96},{"fullName":5,"class":6},"University of Lausanne Hospitals","OTHER",[8],{"label":9,"type":10,"description":10,"interventionNames":11},"multimorbid patients in general internal medicine divisions of all five Swiss university hospitals",null,[12],"Other: Hospitalization",[14],{"type":6,"name":15,"description":16,"armGroupLabels":17,"otherNames":10},"Hospitalization","The investigators collect PROMs amongst up to 1000 patients in general internal medicine divisions of all five Swiss university hospitals",[9],[19,23,26,29],{"name":20,"affiliation":21,"role":22},"Jerome Stirnemann, MD","University Hospital, Geneva","PRINCIPAL_INVESTIGATOR",{"name":24,"affiliation":25,"role":22},"Carole Aubert, MD","Bern University Hospital",{"name":27,"affiliation":28,"role":22},"Florence Vallelian Cervetto, MD","Zürich University Hospital",{"name":30,"affiliation":31,"role":22},"Stefano Bassetti, MD","Basel University Hospital",[33],{"name":34,"role":35,"phone":36,"phoneExt":10,"email":37},"Marie Méan, MD","CONTACT","+41 213141111","marie.mean@chuv.ch",[39],{"facility":40,"status":41,"city":42,"state":43,"zip":44,"country":45,"countryCode":46,"cosmosGeoPoint":47,"geoPoint":52,"contacts":53},"Lausanne University Hospital","RECRUITING","Lausanne","Canton of Vaud","1005","Switzerland","CH",{"type":48,"coordinates":49},"Point",[50,51],6.63282,46.516,{"lat":51,"lon":50},[54],{"name":55,"role":35,"phone":56,"phoneExt":10,"email":10},"Marie Mean","+41213141111",{"type":22,"investigatorFullName":58,"investigatorTitle":59,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"Marie Méan","Principal Investigator, Senior Physician",[61,63,64,66],{"name":62,"class":6},"Insel Gruppe AG, University Hospital Bern",{"name":21,"class":6},{"name":65,"class":6},"University Hospital, Zürich",{"name":67,"class":6},"University Hospital, Basel, Switzerland","100561988","trends-of-patient-reported-outcome-measures-proms-in-multimorbid-medical-patients-hospitalized-for-an-acute-illness-100561988",false,"NCT06597318","Trends of Patient-reported Outcome Measures (PROMs) in Multimorbid Medical Patients Hospitalized for an Acute Illness","TRADUCE","Inclusion Criteria:\n\n* eligible for the LUCID registry (CER-VD AO\\_2023-00029) \\[Age ≥ 18 years, hospitalized in one of the five participating university hospitals (Geneva, Lausanne, Bern, Zürich, Basel), after 01.01.2014, and admitted to general internal medicine wards\n* Multimorbid patients (2 or more chronic diseases, defined as chronic conditions defined by international classification of diseases, 10th revision, codes with an estimated expected duration of at least 6 months or based on a clinical decision.\n* Acute illness\n* Signature of study specific informed consent\n\nExclusion Criteria:\n\n* Not able to speak French, German or English\n* Foreseen length of stay of less than 4 days (estimated by study collaborators)\n* Prior inclusion in the TRADUCE study\n* Incapacity of discernment, i.e. cognitive impairment which could interfere with the ability to fill in PROMs tools","ALL","18 Years",{"count":78,"type":79},1000,"ESTIMATED","OBSERVATIONAL","currently, PROMs and PREMs are not routinely collected and compared among medical inpatients of Swiss university hospitals, nor is a standard set of PROMs and PREMs available for use in Swiss hospitals. The project aims to examine trends in patient-reported outcomes (PROMs), including symptoms, quality of life, and distress, in multimorbid hospitalized patients from admission to 30 days post-discharge. It will also investigate whether PROMs at discharge are linked to the risk of readmission or emergency visits and explore how these outcomes differ in patients who receive low-value care. Additionally, the project will assess the relationship between patient-reported experiences (PREMs) and the provision of low-value care during the hospital stay.",[83,84,85,86],"PROM","PREM","Quality of Care","Internal Medicine","2024-09-12",{"date":89,"type":90},"2024-09-19","ACTUAL",{"date":92,"type":90},"2023-07-01",{"date":94,"type":79},"2025-10-01",{"name":5,"class":6},1]