[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100606469":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":24,"centralContacts":29,"locations":39,"responsibleParty":69,"collaborators":12,"id":71,"slug":72,"hasResults":73,"nctId":74,"briefTitle":75,"officialTitle":75,"acronym":76,"eligibilityCriteria":77,"healthyVolunteers":73,"sex":78,"minAge":79,"maxAge":12,"enrollmentInfo":80,"targetDuration":12,"studyType":83,"phases":84,"briefSummary":86,"conditions":87,"keywords":91,"overallStatus":95,"whyStopped":12,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":105},{"fullName":5,"class":6},"Australian and New Zealand Intensive Care Research Centre","OTHER",[8,13],{"label":9,"type":10,"description":11,"interventionNames":12},"Control: Standard care","NO_INTERVENTION","Paticipants randomised to the control group will not receive the intervention. They will be contacted by the study team to collect data on access to primary health care services post hospital discharge and will be contacted at D90 and D180 by outcome assessors to collected patient reported outcomes.",null,{"label":14,"type":15,"description":16,"interventionNames":17},"Intervention","EXPERIMENTAL","Participants randomised into this group will receive tailored care coordination and support to develop recovery goals post hospital discharge.",[18],"Other: Multicomponent telehealth care coordination",[20],{"type":6,"name":21,"description":22,"armGroupLabels":23,"otherNames":12},"Multicomponent telehealth care coordination","Participants randomised into the intervention group will be assigned a recovery navigator prior to discharge from hospital. The recovery navigator will provide the participant with a study tailored discharge summary, arrange the patients first appointment with their general practitioner and will ensure medications are reconciled prior to hospital discharge. The recovery coordinator will arrange weekly calls with the participant for the first 4 weeks and then fortnightly until week 12 to set recovery goals and assess recovery goals and navigator further primary care support if required. Participants will also be called at Day 90 and 180 by outcome assessors to collected patient reported outcomes.",[14],[25],{"name":26,"affiliation":27,"role":28},"Carol Hodgson, Professor","Monash University","STUDY_CHAIR",[30,35],{"name":31,"role":32,"phone":33,"phoneExt":12,"email":34},"Anne Mather","CONTACT","+61 3 9903 0263","anne.mather@monash.edu",{"name":36,"role":32,"phone":37,"phoneExt":12,"email":38},"Tony Trapani","+61 3 9903 0343","tony.trapani@monash.edu",[40,58],{"facility":41,"status":12,"city":42,"state":43,"zip":44,"country":45,"countryCode":46,"cosmosGeoPoint":47,"geoPoint":52,"contacts":53},"Cabrini Hospital Malvern","Melbourne","Victoria","3144","Australia","AU",{"type":48,"coordinates":49},"Point",[50,51],144.96332,-37.814,{"lat":51,"lon":50},[54],{"name":55,"role":32,"phone":56,"phoneExt":12,"email":57},"Lisa Hodgson, Dougherty","+61 3 9508 1744","icuresearch@cabrini.com.au",{"facility":59,"status":12,"city":42,"state":43,"zip":60,"country":45,"countryCode":46,"cosmosGeoPoint":61,"geoPoint":63,"contacts":64},"Monash Health","3168",{"type":48,"coordinates":62},[50,51],{"lat":51,"lon":50},[65],{"name":66,"role":32,"phone":67,"phoneExt":12,"email":68},"Michelle Paton","+61 3 9594 6666","michelle.paton@monashhealth.org",{"type":70,"investigatorFullName":12,"investigatorTitle":12,"investigatorAffiliation":12,"oldNameTitle":12,"oldOrganization":12},"SPONSOR","100606469","phase-3-improving-survivorship-for-critically-ill-patients-aged-65-and-over-100606469",false,"NCT07175961","Improving Survivorship for Critically Ill Patients Aged 65 and Over","IMPROVE-65","Inclusion Criteria:\n\n* Was admitted to ICU for at least 48 hours\n* is aged 65 years or older at the time of hospital admission\n* Is alive and ready for hospital discharge\n* Is expected to survive for 6 months beyond hospital discharge (e.g. not discharged on palliative care)\n* Has new disability at hospital discharge measured using the global disability scale\n\nExclusion Criteria:\n\n* Is not expected to reside in Australia for 3 months following randomisation.\n* Is not expected to be living at home within 2 weeks of acute hospital discharge (e.g. prolonged inpatient rehabilitation)\n* Is unable to identify a GP or GP clinic and\u002For are unable or unwilling to attend a GP appointment scheduled by the recovery navigator.\n* Has an existing recovery or nurse navigator as part of their routine clinical care to assist with planning their care after hospital discharge","ALL","65 Years",{"count":81,"type":82},300,"ESTIMATED","INTERVENTIONAL",[85],"PHASE3","IMPROVE-65 is a randomised control trial designed specifically for people aged over 65 who have survived critical illness. It aims to support patients and general practitioners by providing timely, personalised information to help them work together to make informed goals and decisions about their care after hospital discharge. The aim of the study is to improve recovery and avoid preventable hospital readmissions.",[88,89,90],"Critical Illness","Recovery Outcomes","Care Coordination",[92,93,94],"critical illness","recovery coordination","patient reported outcomes","NOT_YET_RECRUITING","2025-09-16",{"date":98,"type":99},"2025-09-19","ACTUAL",{"date":101,"type":82},"2025-11",{"date":103,"type":82},"2028-02",{"name":5,"class":6},2]