[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100658697":3},{"organization":4,"outcomesModule":7,"designInfo":133,"detailedDescription":141,"studyPopulation":138,"armGroups":142,"interventions":148,"overallOfficials":153,"centralContacts":157,"locations":138,"responsibleParty":162,"collaborators":138,"id":165,"slug":166,"hasResults":167,"nctId":168,"briefTitle":169,"officialTitle":170,"acronym":171,"eligibilityCriteria":172,"healthyVolunteers":167,"sex":173,"minAge":174,"maxAge":138,"enrollmentInfo":175,"targetDuration":138,"studyType":178,"phases":179,"briefSummary":180,"conditions":181,"keywords":183,"overallStatus":188,"whyStopped":138,"lastUpdateSubmitDate":189,"lastUpdatePostDateStruct":190,"startDateStruct":193,"completionDateStruct":195,"leadSponsor":197,"locationsCount":138},{"fullName":5,"class":6},"Tan Tock Seng Hospital","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":38,"otherOutcomes":120},[9,13,16,20,23,27,31,35],{"measure":10,"description":11,"timeFrame":12},"completion of the Month-6 PICS physical assessment","Physical :5 Times Sit-to-Stand Time in seconds required to complete five sit-to-stand repetitions. Values will be summarized at each assessment time point and change over time described.","From recruitment to 6 months post hospital discharge, or death by any cause, up to 24 months from recruitment",{"measure":14,"description":15,"timeFrame":12},"completion of the Month 6 physical domain assessment","Handgrip strength measured in kilograms using a standardized dynamometer procedure. Values will be summarized at each assessment time point and longitudinal change described.",{"measure":17,"description":18,"timeFrame":19},"completion of Month 6 Cognitive domain assessment","Cognitive function measured using the Mini Mental State examination. Scores will be summarized at each assessment time point and longitudinal change described. MoCA may be used where clinically indicated and will be reported separately rather than treated as equivalent to MMSE.","From recruitment to 6 months post hospital discharge, or death by any cause, up to 24 months from recruitment Time points: (Hospital discharge, 3, 6 month post hospital discharge)",{"measure":21,"description":22,"timeFrame":12},"Completion of Month 6 Mental Domain assessment","Depressive symptoms screened using the Patient Health Questionnaire-9(PHQ-9). Total scores will be summarized at each assessment time point",{"measure":24,"description":25,"timeFrame":26},"Completion of Month 6 Mental Domain Assessment","Anxiety symptoms screened using the GAD-7. Total scores will be summarized at each assessment time point","From recruitment to 6 months post hospital discharge, or death by any cause, up toFrom recruitment to 6 months post hospital discharge, or death by any cause, up to 24 months from recruitment",{"measure":28,"description":29,"timeFrame":30},"Health related quality of life","Health-related quality of life assessed using the EQ-5D-5L. EQ-5D-5L health-state\u002Findex values and EQ visual analogue scale scores will be summarized as applicable at each assessment time point.","from recruitment to 12 months post hospital discharge, or date of death from any cause (time points: 3,6 and 12 months post hospital discharge), up to 24 months from recruitment",{"measure":32,"description":33,"timeFrame":34},"Modified Barthel Index","Functional independence measured using the Modified Barthel Index. Higher scores indicate greater independence in activities of daily living. Scores will be summarized at each assessment time point","From recruitment to 12 months post hospital discharge, or death by any cause up to 24 months from recruitment",{"measure":36,"description":37,"timeFrame":12},"Return to work status","Employment status prior to ICU admission and post hospital discharge will be assessed. Among participants employed before critical illness, the number and percentage who have returned to work will be reported.",[39,43,47,51,54,58,62,66,69,73,77,81,85,89,93,97,101,105,109,113,116],{"measure":40,"description":41,"timeFrame":42},"Feasibility of program","proportion of eligible patients successfully recruited out (screened at ICU discharge)","From start of screening to 12 months post hospital discharge for the last patient recruited (approximately 24 months from start of study)",{"measure":44,"description":45,"timeFrame":46},"Five Times Sit to Stand","Time in seconds required to complete five sit-to-stand repetitions. Values will be summarized at each assessment time point and change over time described.","From recruitment to 6 months post hospital discharge, or death by any cause, up to 24 months from recruitment (time points :at hospital discharge, 3 and 6 months post hospital discharge",{"measure":48,"description":49,"timeFrame":50},"Grip strength","Handgrip strength with dynamometer","From recruitment to 6 months post hospital discharge or date of death from any cause, up to 24 months from recruitment (Time points: ICU discharge, hospital discharge, 3 and 6 months post hospital discharge)",{"measure":32,"description":52,"timeFrame":53},"Functional independence measured using the Modified Barthel Index. Higher scores indicate greater independence in activities of daily living. Scores will be summarized at each assessment time point and longitudinal change described.","From recruitment to 6 months post hospital discharge, or death by any cause, up to 24 months from recruitment (Time points: hospital discharge, 3,6, 12 month post hospital discharge",{"measure":55,"description":56,"timeFrame":57},"Mini-mental state examination","Cognitive function measured using the MMSE. Scores will be summarized at each assessment time point and longitudinal change described. MoCA may be used where clinically indicated and will be reported separately rather than treated as equivalent to MMSE.","From recruitment to 6 months post hospital discharge, up to 24 months from recruitment Time points: (Hospital discharge, 3, 6 month post hospital discharge)",{"measure":59,"description":60,"timeFrame":61},"Patient health questionnaire -9","Depressive symptoms measured using the PHQ-9. Total scores will be summarized at each assessment time point and longitudinal change described.","From recruitment to 6 months post hospital discharge, or death by any cause, up to 24 months from recruitment (Time points :Hospital discharge, 3, 6 month post hospital discharge)",{"measure":63,"description":64,"timeFrame":65},"General anxiety scale-7","Anxiety symptoms measured using the GAD-7. Total scores will be summarized at each assessment time point and longitudinal change described.","From recruitment up to 24 months from recruitment (time points: hospital discharge, 3,6 month post hospital discharge)",{"measure":67,"description":68,"timeFrame":12},"Retention at 6 months","Number of ICU survivors who have not withdrawn\u002F lost to follow up compared to original recruited number (excluding deaths)",{"measure":70,"description":71,"timeFrame":72},"Completion of planned home visits","Monthly home visits x6 are planned per ICU survivor Number of planned home visits declined\u002F lost to follow up amongst survivors (excluding deaths) 3 and 6 month home visits converted to telehealth\u002F hospital visits","6 months post hospital discharge, up to 24 months from recruitment",{"measure":74,"description":75,"timeFrame":76},"UCLA loneliness scale-3","University of California Los Angeles loneliness scale-3","from recruitment up to 24 months post recruitment (time points 1,4 12 months post hospital discharge)",{"measure":78,"description":79,"timeFrame":80},"Caregiver burden","Caregiver burden will be measured using the shortened 9-item Zarit Burden Interview (ZBI-9), with scores summarized over follow-up.","From recruitment to 6 months post hospital discharge, or patient death by any cause , up to 24 hours post recruitment (Time points :1 and 6 months post hospital discharge)",{"measure":82,"description":83,"timeFrame":84},"reasons for non-participation or declining home visits","reasons for non-participation of home visits","at the point of enrolment into home visits at hospital discharge up to 6 months post hospital discharge, or death from any cause, whichever comes first , up to 24 months from recruitment",{"measure":86,"description":87,"timeFrame":88},"Medication or follow-up appointment reconciliation events","number of medication or follow up appointment reconciliation events done during home visits, per home visit","6 months post hospital discharge, from recruitment up to 24 months from recruitment",{"measure":90,"description":91,"timeFrame":92},"Swallowing status","In- hospital, oral intake and swallowing status assessed using the Functional Oral Intake Scale. EAT-10 questionnaire post hospital discharge; Scores will be summarized descriptively over follow-up.","From recruitment into study, up 24 months from recruitment, or death by any cause, whichever first (time points: at the Icu discharge, hospital discharge, 2 and 5 months post hospital discharge",{"measure":94,"description":95,"timeFrame":96},"Body weight","Contributes to nutritional assessment Body weight measured in kilograms and summarized at each assessment time point and longitudinally.","From recruitment into study, up to 24 months from recruitment, or death from any cause, whichever comes first (time points: pre ICU, at the Icu discharge, hospital discharge, 2 and 5 months post hospital discharge",{"measure":98,"description":99,"timeFrame":100},"arm and leg circumference","arm and leg circumference as a surrogate for nutritional status and muscle bulk.\n\nExcludes patients who have contraindications e.g. loss of limb, abnormal BMI, edema","From recruitment into study, up to 24months from recruitment or death from any cause, whichever comes first (Time points: at the Icu discharge, hospital discharge, 2 and 5 months post hospital discharge)",{"measure":102,"description":103,"timeFrame":104},"Chelsea Critical Care Physical Assessment tool","CPax","From recruitment into study, up to death from any cause or 24 months from recruitment, whichever comes first.",{"measure":106,"description":107,"timeFrame":108},"Montreal Cognitive Assessment Tool","MoCA assessment for patients screened with MMSE and have high suspicion of cognitive impairment","From recruitment into study, 6 months post hospital discharge, or date of death from any cause, whichever comes first (if applicable)",{"measure":110,"description":111,"timeFrame":112},"healthcare utilisation","number of unplanned clinic visits, emergency department visits, unplanned admissions with reference from point of hospital discharge","12 months post hospital discharge",{"measure":114,"description":114,"timeFrame":115},"mortality","From recruitment to 12 months post hospital discharge, up till 24 months from recruitment, or death by any cause, whichever comes first",{"measure":117,"description":118,"timeFrame":119},"return to work status","for survivors who were working pre ICU admission, the number who returned to work","From recruitment until 24 months from recruitment (time points: 3,6 12 months post hospital discharge)",[121,125,129],{"measure":122,"description":123,"timeFrame":124},"life-space","Life space at month 3, 6, 12 post hospital discharge","From recruitment to 24 months from recruitment, or death from any cause, whichever comes first (Time points: Pre ICU admission, 3,6 and 12 months)",{"measure":126,"description":127,"timeFrame":128},"Clinical Frailty Scale","trajectory of CFS over time. Scores will be summarized descriptively across assessment time points.","From hospital admission up to 24 months from recruitment (Time points: pre-ICU baseline , hospital discharge, 3, 6, 12 months post hospital)",{"measure":130,"description":131,"timeFrame":132},"User acceptability","acceptability of the program and free text comments","From recruitment up till 24 months from recruitment or date of death from any cause (Time points: 6 and 12 month post hospital discharge )",{"allocation":134,"interventionModel":135,"interventionModelDescription":136,"primaryPurpose":137,"observationalModel":138,"timePerspective":138,"maskingInfo":139},"NA","SINGLE_GROUP","This is a prospective, single-centre study using a Type 3 hybrid implementation-effectiveness feasibility design, as described by Curran et al.\n\nThe study is designed to evaluate whether THRIVE@TTSH can be delivered within routine clinical and community workflows. Implementation outcomes will be informed by Proctor's framework, including feasibility, acceptability and fidelity. RE-AIM (Reach, Effectiveness, Adoption, Implementation and Maintenance) will provide the broader reporting framework; effectiveness outcomes will be exploratory","HEALTH_SERVICES_RESEARCH",null,{"masking":140,"maskingDescription":138,"whoMasked":138},"NONE","This is a prospective, single-centre hybrid implementation-effectiveness feasibility study which will recruit 50 adult ICU survivors over 12 months. Assessments will occur during hospitalisation and at Months 3 and 6 after hospital discharge, with a final phone follow-up at Month 12. There will be volunteer-supported home visits for 6 months post hospital discharge. The primary feasibility outcome is the proportion of enrolled participants alive at Month 6 who complete outcome assessment.\n\nSecondary implementation outcomes include recruitment, retention, home-visit completion and acceptability. Exploratory outcomes include Post ICU Syndrome (PICS) recovery trajectories, healthcare utilisation and mortality through 12 months post discharge from the acute hospital.",[143],{"label":144,"type":145,"description":138,"interventionNames":146},"Single arm feasibility study","EXPERIMENTAL",[147],"Other: THRIVE@TTSH follow up program",[149],{"type":6,"name":150,"description":151,"armGroupLabels":152,"otherNames":138},"THRIVE@TTSH follow up program","1. Structured post-ICU screening\n2. Comprehensive multidomain assessment\n3. Personalised ICU recovery summary\n4. Multidisciplinary review and closed-loop care coordination\n5. Volunteer-supported home follow-up and multidisciplinary meetings",[144],[154],{"name":155,"affiliation":5,"role":156},"Yie Hui Lau","PRINCIPAL_INVESTIGATOR",[158],{"name":155,"role":159,"phone":160,"phoneExt":138,"email":161},"CONTACT","+65 63577771","yie.hui.lau@nhghealth.com.sg",{"type":156,"investigatorFullName":163,"investigatorTitle":164,"investigatorAffiliation":5,"oldNameTitle":138,"oldOrganization":138},"Lau Yie Hui","Senior Consultant","100658697","protocol-for-a-hybrid-implementation-effectiveness-feasibility-study-of-a-transdisciplinary-icu-to-home-recovery-model-100658697",false,"NCT07854080","Protocol for a Hybrid Implementation-effectiveness Feasibility Study of a Transdisciplinary ICU-to-home Recovery Model","Transition Support and Holistic Recovery Interventions for Vulnerable Ex-ICU Patients @ Tan Tock Seng Hospital (THRIVE@TTSH): Protocol for a Hybrid Implementation-effectiveness Feasibility Study of a Transdisciplinary ICU-to-home Recovery Model","THRIVE@TTSH","Inclusion criteria\n\n1. Received invasive mechanical ventilation for ≥ 48 hours;\n2. Aged ≥ 21 years;\n3. Premorbidly independent in basic activities of daily living;\n4. Had decision-making capacity before the acute illness and are expected to regain capacity before acute hospital discharge;\n5. Have evidence of new or worsening physical, cognitive, mental-health or swallowing impairment compared with their premorbid state; and\n6. Are ultimately planned for discharge to the community\u002Fhome setting. Worsening in PICS domains is defined as an increase in CFS score compared with premorbid status, newly acquired swallowing dysfunction, new cognitive impairment after exclusion of delirium, suspected anxiety or depressive symptoms, or clinically important deterioration in physical or functional performance.\n\nMental-health screening will not be interpreted as diagnostic criteria for anxiety or depressive disorders.\n\nExclusion criteria\n\n* cognitive or psychiatric impairment that precludes meaningful participation in the study;\n* are already enrolled in, or expected to enter, a structured follow-up pathway that substantially duplicates the rehabilitation intervention; or\n* have treatment primarily directed towards palliation or end-of-life care","ALL","21 Years",{"count":176,"type":177},50,"ESTIMATED","INTERVENTIONAL",[134],"This is a prospective, single-centre study which will recruit 50 adult ICU survivors over 12 months. Assessments will occur during hospitalisation and at Months 3 and 6 after hospital discharge, with a final phone follow-up at Month 12. There will be volunteer-supported home visits for 6 months post hospital discharge.",[182],"Post ICU Syndrome",[184,185,186,187],"post icu syndrome","critical care","implementation study","rehabilitation","NOT_YET_RECRUITING","2026-09-30",{"date":191,"type":192},"2026-10-02","ACTUAL",{"date":194,"type":177},"2026-10-31",{"date":196,"type":177},"2028-12-31",{"name":5,"class":6}]