[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100304680":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":12,"centralContacts":20,"locations":30,"responsibleParty":47,"collaborators":10,"id":49,"slug":50,"hasResults":51,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":51,"sex":57,"minAge":58,"maxAge":10,"enrollmentInfo":59,"targetDuration":10,"studyType":62,"phases":10,"briefSummary":63,"conditions":64,"keywords":66,"overallStatus":33,"whyStopped":10,"lastUpdateSubmitDate":74,"lastUpdatePostDateStruct":75,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":83},{"fullName":5,"class":6},"Radboud University Medical Center","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":10},"Cohort",null,"Critically ill patients admitted \\>12 hours to the ICU",[13,17],{"name":14,"affiliation":15,"role":16},"Mark van den Boogaard, RN, PhD.","Radboud university medical center, Prof.dr. of Nursing Science in Acute and Critical Care","PRINCIPAL_INVESTIGATOR",{"name":18,"affiliation":19,"role":16},"Marieke Zegers, PhD","Radboud university medical center, Senior Researcher dep of Intensive Care Medicine",[21,26],{"name":22,"role":23,"phone":24,"phoneExt":10,"email":25},"Mark van den Boogaard, RN, PhD","CONTACT","0031-243665009","Mark.vandenBoogaard@radboudumc.nl",{"name":27,"role":23,"phone":28,"phoneExt":10,"email":29},"Marieke Zegers, PhD.","0031-243619269","Marieke.Zegers@radboudumc.nl",[31],{"facility":32,"status":33,"city":34,"state":10,"zip":35,"country":36,"countryCode":37,"cosmosGeoPoint":38,"geoPoint":43,"contacts":44},"Radboud university medical center","RECRUITING","Nijmegen","6500 HB","Netherlands","NL",{"type":39,"coordinates":40},"Point",[41,42],5.85278,51.8425,{"lat":42,"lon":41},[45,46],{"name":14,"role":23,"phone":24,"phoneExt":10,"email":25},{"name":27,"role":23,"phone":28,"phoneExt":10,"email":29},{"type":48,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100304680","monitor-ic-determining-and-improving-long-term-consequences-of-icu-care-100304680",false,"NCT03246334","MONITOR-IC: Determining and Improving Long-term Consequences of ICU Care","MONITOR-IC: a Mixed Methods Multicenter Prospective Open Cohort Study Determining and Improving Long-term Outcomes of ICU Survivors","MONITOR-IC","Inclusion Criteria:\n\n* ICU patients age 16 years or older;\n* admitted at least 12 hours to a trauma, medical, neurosurgery or cardiac surgery ICU;\n* gave written informed consent (or by their legal representative).\n\nExclusion Criteria:\n\n* Patients with a life expectancy of \\\u003C48 hours;\n* receive palliative care;\n* are admitted for a donor procedure;\n* cannot read and speak the Dutch language;\n* or are not able to fill in the questionnaire and do not have family members\u002F legal representatives either.","ALL","16 Years",{"count":60,"type":61},50000,"ESTIMATED","OBSERVATIONAL","Due to advances in critical care medicine, more patients survive their critical illness. However, intensive care unit (ICU) survivors often experience long-term physical, cognitive and mental problems, summarized as post intensive care syndrome (PICS), impacting their health related quality of life (HRQoL).\n\nThe aims of this study are to study the: 1) long-term outcomes, 2) predictors for PICS, 3) prediction of long-term HRQoL, 4) ratio between HRQoL of ICU-survivors and healthcare related costs, and 5) effects on the long-term of interventions",[65],"Post-Intensive Care Syndrome (PICS)",[67,68,69,70,71,72,73],"Cohort study","Critical Care","Follow-up study","Intensive care units","Long-term outcome","Outcome assessment","Quality of life","2023-12-20",{"date":76,"type":77},"2023-12-27","ACTUAL",{"date":79,"type":77},"2016-07-01",{"date":81,"type":61},"2050-08",{"name":5,"class":6},1]