[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"transition-of-care\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:transition-of-care":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,59,89],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":46,"whyStopped":4,"lastUpdateSubmitDate":47,"lastUpdatePostDateStruct":48,"startDateStruct":51,"completionDateStruct":53,"leadSponsor":55,"locationsCount":58},"100632819","feasibility-of-the-transitioned-framework-for-youth-and-young-adults-with-eating-disorders-100632819",false,"NCT07518641","Feasibility of the TransitionED Framework for Youth and Young Adults With Eating Disorders","TransitionED 3","Inclusion Criteria:\n\nYouth and Young Adults (YYA):\n\n* Currently receiving paediatric eating disorder care at a participating study site.\n* Age 16 years or or older (approaching age-based transition to adult-care)\n* Expressed interest in transitioning to adult eating disorder care or other appropriate adult mental health services\n* Identified by the clinical team as appropriate to begin formal transition planning (e.g., sufficient transition readiness and interest in ongoing care)\n* Able and willing to provide informed consent\u002Fassent (as applicable at the site) and participate in study procedures\n\nCaregivers:\n\n* One caregiver (e.g., parent\u002Flegal guardian) of a participating YYA\n* Able and willing to provide informed consent and participate in study procedures (including questionnaires and interviews)\n\nClinicians (intervention deliverers):\n\n* Patient facing clinician at a participating site who provides transition support for participating YYA\u002Fcaregivers and is responsible for delivering intervention components (e.g., joint meeting(s), communication\u002Fcoordination related to the transition).\n* Able and willing to provide informed consent and participate in study procedures (e.g., focus groups)\n\nImplementation Team Members:\n\n* Program leadership\u002Fmanagers\u002Fsenior clinicians at a participating site involved in implementation of the intervention at that site.\n* Able and willing to provide informed consent and participate in study procedures (e.g., focus group).\n\nExclusion Criteria:\n\nYYA:\n\n* Not receiving pediatric eating disorder care at a participating site.\n* Under age 16 years\n* Does not express interest in transitioning to adult eating disorder care or other appropriate adult mental health services.\n* Not identified by the clinical team as ready\u002Fappropriate to engage in formal transition planning during the study period (e.g., insufficient transition readiness or not currently at the transition-planning stage).\n* Unable to provide informed consent\u002Fassent or unable to participate in study procedures (e.g., due to significant cognitive\u002Fcommunication barriers as determined by the clinical\u002Fresearch team).\n\nCaregivers:\n\n* Not the caregiver of an enrolled YYA (only one caregiver per YYA is enrolled).\n* Unable to provide informed consent or participate in study procedures.\n\nClinicians and Implementation Team Members:\n\n* Not affiliated with a participating site or not in an eligible role as defined above.\n* Peripheral providers who may be involved in care but are not enrolled as participants (e.g., family physicians or adult providers who might attend a joint meeting).\n* Unable to provide informed consent or participate in study procedures.","ALL","16 Years",{"count":19,"type":20},60,"ESTIMATED","INTERVENTIONAL",[23],"NA","Moving from pediatric (children's) health care to adult health care can be challenging for youth and young adults with eating disorders. Many young people and families report feeling unprepared, unsure of what to expect, and worried about losing support during this time. Gaps in care during this transition can increase stress and make recovery more difficult.\n\nThis study is testing a structured transition support program called the TransitionED framework. The goal is to see whether this program can be successfully used in real hospital settings and whether youth, caregivers, and clinicians find it helpful.\n\nThe TransitionED framework is designed to help youth and families prepare for the move to adult care. It includes:\n\n1. A transition planning package for youth\n2. A separate planning package for caregivers\n3. At least two guided transition meetings with a clinician\n4. A short \"Personal Transition Profile\" written by the youth to help new adult providers understand them better\n5. Optional virtual peer support sessions for youth and for caregivers\n6. Tools to help pediatric and adult providers communicate more clearly\n\nYouth who are 16 years or older and currently receiving care in a participating pediatric eating disorder program may be invited to join, along with one caregiver. Clinicians and program leaders will also take part to help deliver and evaluate the program.\n\nParticipants will complete surveys at the beginning of the study, about two months later, and six months after finishing the program. Some participants will also take part in interviews to share their experiences.\n\nThis study is focused on feasibility. That means the main goal is to learn whether this transition program is practical, acceptable, and workable in everyday clinical care. What we learn will help improve transition support for youth and young adults with eating disorders in the future.",[26,27],"Eating Disorders in Adolescence","Transition of Care",[29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45],"eating disorders","healthcare transitions","Transition to Adult Care","Adolescent health","Young adults","Paediatric to adult care","Continuity of care","Mental Health Services","Implementation science","Feasibility study","Mixed Methods","Clinical Practice guidelines","Transition readiness","TRAQ","Peer support","Eating disorder treatment","Knowledge translation","NOT_YET_RECRUITING","2026-04-02",{"date":49,"type":50},"2026-04-08","ACTUAL",{"date":52,"type":20},"2026-05",{"date":54,"type":20},"2028-03-31",{"name":56,"class":57},"McMaster University","OTHER",2,{"id":60,"slug":61,"hasResults":11,"nctId":62,"briefTitle":63,"officialTitle":63,"acronym":64,"eligibilityCriteria":65,"healthyVolunteers":11,"sex":16,"minAge":66,"maxAge":4,"enrollmentInfo":67,"targetDuration":4,"studyType":21,"phases":69,"briefSummary":70,"conditions":71,"keywords":74,"overallStatus":78,"whyStopped":4,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":82,"completionDateStruct":84,"leadSponsor":86,"locationsCount":58},"100534851","transition-to-cardiac-rehabilitation-t2cr-to-address-barriers-of-multimorbidity-and-frailty-100534851","NCT06244199","Transition to Cardiac Rehabilitation (T2CR) to Address Barriers of Multimorbidity and Frailty","T2CR","Inclusion Criteria:\n\n* Eligible candidates will consist of male and female Veterans hospitalized with:\n\n  * ischemic heart disease (acute myocardial infarction or stable ischemia)\n* revascularization (coronary artery bypass grafting or percutaneous coronary intervention)\n* valvular heart disease (surgical or percutaneous intervention for mitral regurgitation or aortic stenosis)\n* or heart failure (with reduced or preserved ejection fraction)\n* All will be recruited while initially hospitalized and must express willingness to consider cardiac rehabilitation as a treatment option, including the possibility of the intervention which could possibly extend the length of their hospitalization (for 2 days maximum).\n* Study candidates must also be English speaking and able to provide written informed consent\n\nExclusion Criteria:\n\n* Veterans with unstable medical condition as indicated by history, physical exam, and\u002For laboratory findings end-stage disease likely to be fatal within 12 months\n* severe cognitive impairment (MiniCog score 0-2)\n* history of addictive or behavioral issues that confound safe administration of HBCR\n* hearing loss that interferes with participation in the trial\n* living in a long-term care living situation prior to the time of hospitalization, no plans to return to independent living after the hospitalization","18 Years",{"count":68,"type":20},250,[23],"Cardiac rehabilitation (CR) is a secondary prevention program for patients with cardiovascular disease (CVD). It is especially valuable as CVD increasingly occurs in combination with comorbidity, frailty, and complexities of care that predispose patients to functional decline, disability, and high costs. Still, few Veterans participate in CR, in part because of the difficult logistics to attend. Promising Practice home-based CR (HBCR) was developed to increase CR participation, but many Veterans remain too limited by comorbidity and frailty for participation. A Transition to CR (T2CR) intervention is a face-to-face program that fosters vital skills, education, insights, motivation, and patient-provider relationships conducive to successful HBCR thereafter. This study compares Veterans eligible for CR who are randomized to T2CR intervention versus usual care. Differences in functional capacity, HBCR participation, and healthy days at home are compared over one year. Patients' experiences and providers' perspectives of barriers and facilitators to T2CR are also compared.",[72,73,27],"Cardiovascular Diseases","Cardiac Rehabilitation",[75,76,77],"cardiovascular diseases","cardiac rehabilitation","transition of care","RECRUITING","2025-10-21",{"date":81,"type":50},"2025-10-22",{"date":83,"type":50},"2024-11-01",{"date":85,"type":20},"2027-08-31",{"name":87,"class":88},"VA Office of Research and Development","FED",{"id":90,"slug":91,"hasResults":11,"nctId":92,"briefTitle":93,"officialTitle":94,"acronym":95,"eligibilityCriteria":96,"healthyVolunteers":97,"sex":16,"minAge":98,"maxAge":4,"enrollmentInfo":99,"targetDuration":4,"studyType":101,"phases":4,"briefSummary":102,"conditions":103,"keywords":4,"overallStatus":46,"whyStopped":4,"lastUpdateSubmitDate":110,"lastUpdatePostDateStruct":111,"startDateStruct":113,"completionDateStruct":115,"leadSponsor":117,"locationsCount":4},"100586133","palliative-assessment-cohort-in-the-geriatric-emergency-setting-100586133","NCT06911411","PALLIATIVE ASSESSMENT COHORT IN THE GERIATRIC EMERGENCY SETTING","PALLIATIVE ASSESSMENT AND MANAGEMENT IN THE GERIATRIC EMERGENCY SETTING (PALMA)","PALMA cohort","Inclusion Criteria: Older patient \\>64 years acutely admitted to the geriatric emergency department -\n\nExclusion Criteria: Severe cognitive impairment. Not able to provide informed consent. Not reading Danish\n\n\\-",true,"65 Years",{"count":100,"type":20},300,"OBSERVATIONAL","The PALMA project is part of a larger palliative research program COPAL in Capital Region of Denmark led by Professor Tom Møller. PALMA aims to improve palliative care for geriatric patients transitioning from emergency-hospital to primary care. The project addresses the lack of a systematic approach for assessing and managing palliative symptoms in geriatric patients to enhance communication between hospitals and municipal health care services.\n\nThe PALMA cohort investigates the applicability of systematic palliative assessment (EORTC-C15 PAL) in the geriatric emergency setting combined with measures of frailty, socio-demographic risks, and cross-sectoral healthcare support.",[104,105,106,107,108,109,27],"Geriatric","Palliative Care","Socio-demographic Risk","Frailty at Older Adults","Loneliness","Collaborative Care","2025-03-28",{"date":112,"type":50},"2025-04-04",{"date":114,"type":20},"2025-04-01",{"date":116,"type":20},"2026-12-30",{"name":118,"class":57},"University Hospital Bispebjerg and Frederiksberg"]