[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"home-care-services\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:home-care-services":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,47,71,101,126,160],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":32,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100641485","nurse-led-integrated-home-service-to-support-parents-in-symptom-management-for-children-requiring-respiratory-support-100641485",false,"NCT07652268","Nurse-led Integrated Home Service to Support Parents in Symptom Management for Children Requiring Respiratory Support","Nurse-led Integrated Home Health Service to Support Parents in Symptom Management for Children With Respiratory Support: an Effectiveness-implementation Hybrid 2 Study","Inclusion Criteria:\n\n1. parent of a child with respiratory support aged 6-month to 22 years old\n2. having a Smartphone\n3. able to communicate in Chinese or in English\n4. living with his\u002Fher child at home.\n\nExclusion Criteria:\n\n1. a reported mental health disorder\n2. engaging in other structured programs related to symptom management\n3. living in an area with no internet coverage","ALL","6 Months","22 Years",{"count":20,"type":21},80,"ESTIMATED","INTERVENTIONAL",[24],"NA","The aims of this study are to test the effectiveness of a nurse-led integrated home health service to enhance parental self-efficacy in symptom management for children requiring respiratory support, and alongside identify factors facilitating or deterring the program implementation.\n\nA single group pre-post quasi-experimental study on parents of CMC requiring respiratory support.\n\nParents will be recruited from non-government organizations, with an estimated sample size of 80 parents. Self-administrated questionnaire, and semi-structured interview guide will be used for data collection.",[27,28,29,30,31],"Children With Medical Complexity (CMC)","Symptom Management","Nurse-led Supportive Care","Self Efficacy","Home Care Services",[33],"Children requiring respiratory support","NOT_YET_RECRUITING","2026-06-16",{"date":37,"type":38},"2026-06-18","ACTUAL",{"date":40,"type":21},"2026-07-27",{"date":42,"type":21},"2029-06-30",{"name":44,"class":45},"Dr Winsome Lam","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":16,"minAge":54,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":22,"phases":57,"briefSummary":58,"conditions":59,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":46},"100579096","acute-hospital-care-at-home-for-people-living-with-dementia-100579096","NCT06819852","Acute Hospital Care at Home for People Living With Dementia","Skipping the Hospital: Acute Hospital Care at Home for People Living With Dementia","Inclusion Criteria:\n\n* Diagnosis of moderate or severe dementia (as ascertained by the Quick Dementia Rating System; QDRS)\n* Resides in a private or assisted living residence with or nearby (\\\u003C15min travel time) to a family caregiver\n* Resides within the Mass General Brigham (MGB) home hospital catchment area\n* Has had at least 1 hospitalization in the last 12 months.\n\nExclusion Criteria:\n\n* No functioning utilities, such as no working heat (October-April), no running water, or no electricity.\n* Resides in skilled nursing facility\n* Resides in group home\n* Domestic violence screen positive\n* In police custody\n* Family caregiver unable to initiate or maintain communication with care team\n* End-stage renal disease on hemodialysis\n* On methadone requiring daily pickup of medication\n* Active substance use disorder, without functioning treatment plan\n* Psychiatric diagnosis that would prohibit successful home hospital care\n* Acute delirium without explanation or without the ability to manage at home\n* Patients with cancer requiring consistent hospital-based treatments\n* Cannot ambulate to bedside commode with assistance present in the home (if different from baseline), unless home-based aides are available","18 Years",{"count":56,"type":21},200,[24],"The investigators will perform a parallel-group multicenter randomized controlled trial of a 1-year pre-enrolled acute hospital care at home intervention vs usual care for people living with dementia. Patients will be randomized only after eligibility determination and after the family caregiver agrees to enroll; people living with dementia will assent when able. Patients will be allocated in a concealed fashion to the control and intervention groups in randomly selected block sizes of 4 or 6 in 4 strata reflecting their functional status (activities of daily living: 0, 1, 2-3, 4-6). Although family and clinicians cannot be blinded, the investigators will blind the data collectors and assessors.",[60,31,61],"Emergency Department Visit","Dementia","2026-03-16",{"date":64,"type":38},"2026-03-17",{"date":66,"type":21},"2026-04",{"date":68,"type":21},"2028-05",{"name":70,"class":45},"Brigham and Women's Hospital",{"id":72,"slug":73,"hasResults":11,"nctId":74,"briefTitle":75,"officialTitle":75,"acronym":4,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":16,"minAge":77,"maxAge":4,"enrollmentInfo":78,"targetDuration":4,"studyType":80,"phases":4,"briefSummary":81,"conditions":82,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":46},"100629258","home-based-acute-care-for-older-persons-initiated-by-the-emergency-medical-and-ambulance-services---a-retrospective-observation-of-effects-on-healthcare-utilisation-and-mortality-100629258","NCT07472335","Home-based Acute Care for Older Persons Initiated by the Emergency Medical and Ambulance Services - a Retrospective Observation of Effects on Healthcare Utilisation and Mortality","Inclusion Criteria:\n\n* Contact with the emergency number (112), followed by either a telephone assessment by the Emergency Medical Dispatch Centre or an in-home assessment by an ambulance nurse\n* Home-based acute care a weekday between 8 AM - 4 PM\n* Emergency-department care weeknight 4 PM - 8 AM or weekends\n* Registered residence in one of the municipalities of Gothenburg, Mölndal, Partille, or Härryda\n\nExclusion Criteria:\n\n* Immediate conditions requiring hospital care\n* Care at the emergency department or by a mobile primary care team occurring more than 24 hours after assessment by the Emergency Medical Dispatch Centre or ambulance services\n* Individuals who have already been assessed by a physician and\u002For have a written referral to the emergency department","75 Years",{"count":79,"type":21},5000,"OBSERVATIONAL","This observational study aims to examine outcomes of home-based acute care delivered by a mobile healthcare team in persons aged 75 years and older following an episode of acute illness.\n\nThe study will assess whether home-based acute care initiated by the emergency medical dispatch centre or ambulance services is non-inferior to emergency department care with regard to care needs and mortality.",[83,84,31,85,86,87,88,89,90,91],"Aged","Home Care, Hospital-Based","Emergency Medical Dispatch Centre","Emergency Medical Services","Ambulances","Emergency Service, Hospital","Acute Disease","Mortality","Treatment Outcome","2026-03-10",{"date":62,"type":38},{"date":95,"type":21},"2026-04-01",{"date":97,"type":21},"2027-12-31",{"name":99,"class":100},"Vastra Gotaland Region","OTHER_GOV",{"id":102,"slug":103,"hasResults":11,"nctId":104,"briefTitle":105,"officialTitle":106,"acronym":107,"eligibilityCriteria":108,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":109,"targetDuration":4,"studyType":80,"phases":4,"briefSummary":110,"conditions":111,"keywords":112,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":117,"lastUpdatePostDateStruct":118,"startDateStruct":120,"completionDateStruct":122,"leadSponsor":124,"locationsCount":4},"100600593","factors-influencing-home-nursing-care-service-100600593","NCT07099508","Factors Influencing Home Nursing Care Service","Factors Influencing Home Nursing Care Service: a Pilot Study Shedding Light Over the Feasibility","HoNuCaS-01","Inclusion Criteria: all patients receiving home care nursing services who agree to voluntary participation",{"count":56,"type":21},"This pilot study investigates the feasibility of a prospective longitudinal observational approach to identify variables influencing home nursing care time. Conducted within the ULSS 6 Euganea health district in Italy, the study will analyze nursing care and travel time across approximately 350 home visits involving up to 200 voluntarily enrolled adult patients. Data will be collected anonymously by nurses using a digital tool (REDCap), capturing a predefined core set of variables previously selected via the Delphi method. The study aims to understand the association between individual, contextual, and organizational variables and the time required for home nursing interventions. Results will inform better planning and resource allocation for home care services.",[31],[113,114,115,116],"Home Nursing Care","Nursing time measurement","Travel time","Health planning","2025-07-25",{"date":119,"type":38},"2025-08-01",{"date":121,"type":21},"2025-09",{"date":123,"type":21},"2025-11",{"name":125,"class":45},"University of Padova",{"id":127,"slug":128,"hasResults":11,"nctId":129,"briefTitle":130,"officialTitle":131,"acronym":132,"eligibilityCriteria":133,"healthyVolunteers":11,"sex":16,"minAge":134,"maxAge":4,"enrollmentInfo":135,"targetDuration":4,"studyType":22,"phases":137,"briefSummary":138,"conditions":139,"keywords":142,"overallStatus":150,"whyStopped":4,"lastUpdateSubmitDate":151,"lastUpdatePostDateStruct":152,"startDateStruct":154,"completionDateStruct":156,"leadSponsor":158,"locationsCount":46},"100579106","autonomous-at-home-with-occupational-therapy-support-and-assistive-devices-100579106","NCT06819982","Autonomous At Home with Occupational Therapy Support and Assistive Devices","Autonome À Domicile Grâce À Un Appareil Connecté Et À Un Suivi Ergo","AUDACE","Inclusion Criteria:\n\n* people aged 65 and over\n* living at home in the Walloon and Brussels regions\n* who are considered frail or at risk of frailty. The risk of frailty is defined as having at least one loss of intrinsic capacity measured by a trained occupational therapist using the ICOPE screening tool\n\nExclusion Criteria:\n\n* People benefiting from other AViQ autonomy programmes of this project are excluded","65 Years",{"count":136,"type":21},3900,[24],"The aim of the AUDACE study is to evaluate the 'Bien chez Moi 2.0' programme, to assess how, for whom and why do assistive devices, integrated with occupational therapy support, enable older people to remain at home, and under what conditions? The study assesses the impact on areas such as the degree of autonomy, the extent to which life goals are taken into account, the feeling of security at home, the use of hospital emergency services and the postponement of definitive institutionalisation in a nursing home. The expected results of this study are to be able to robustly describe the impact of the 'Bien chez moi 2.0' programme in the areas listed above.",[140,141,31],"Frailty","Aging",[143,31,144,145,146,147,148,149],"Education, Continuing","Monitoring, Ambulatory","Occupational Therapy","Personal Autonomy","Primary Health Care \u002F methods","Program Evaluation","Self-Help Devices","RECRUITING","2025-02-05",{"date":153,"type":38},"2025-02-11",{"date":155,"type":38},"2024-03-04",{"date":157,"type":21},"2025-09-04",{"name":159,"class":45},"Université Catholique de Louvain",{"id":161,"slug":162,"hasResults":11,"nctId":163,"briefTitle":164,"officialTitle":165,"acronym":166,"eligibilityCriteria":167,"healthyVolunteers":11,"sex":16,"minAge":168,"maxAge":4,"enrollmentInfo":169,"targetDuration":4,"studyType":22,"phases":171,"briefSummary":172,"conditions":173,"keywords":4,"overallStatus":150,"whyStopped":4,"lastUpdateSubmitDate":177,"lastUpdatePostDateStruct":178,"startDateStruct":180,"completionDateStruct":182,"leadSponsor":184,"locationsCount":5},"100488151","supportive-care-at-home-research-for-patients-with-advanced-cancer-stahr-cancer-100488151","NCT05636384","SupporTive Care At Home Research for Patients With Advanced Cancer (STAHR-cancer)","SupporTive Care At Home Research (STAHR): a Cluster Non-randomized Controlled Trial for Patients With Advanced Cancer","HOMECARE","Inclusion Criteria:\n\nBoth the patient and their family caregiver must meet the criteria to be considered for this research.\n\n1. Patient\n\n   1. A person who has an advanced-stage solid cancer diagnosis (ICD-10 code C00-C70); A person who is receiving or planning to receive cancer treatment\n   2. A person who meets one of the following conditions\n\n      1. Has been evaluated as having ECOG performance status 2\n      2. Has been evaluated as having ECOG performance status 1 and is over 70 years of age\n   3. A person who wishes to stay at home\n   4. A person whose family caregiver resides at home\n   5. A person who wishes to participate in the research\n2. Family Caregiver\n\n   1. A family\\* member of the patient\n\n      \\* Family: refers to the patient's spouse (including a common-law partner), descendants and their spouses up to the second degree, siblings and their spouses, and relatives and their spouses up to the eighth degree.\n   2. A person who meets one of the following conditions:\n\n      1. Lives with the patient (patient's household member)\n      2. Does not live with the patient, but visits the patient's home more than three times a week\n   3. A person who wants the patient to stay at home\n   4. A person who can communicate easily with medical staff\n   5. A person who wishes to participate in the research\n\nExclusion Criteria:\n\nIf either the patient or the family caregiver meets any one of these criteria, they are excluded from the study.\n\n1. Patient\n\n   1. A person who cannot speak, hear, or read Korean\n   2. A person who is judged by a medical doctor to be unable to take part in this research due to extremely poor health\n   3. A person residing outside the range that can be visited by the respective medical institution (the conditions for distance are to be specified by each medical institution)\\*\n\n      \\* This condition is not applicable for the control group.\n   4. A person who has used hospital- or home-type hospice and palliative care services\n   5. A person who is under the age of 19\n2. Family Caregiver\n\n   1. A person who cannot speak, hear, or read Korean\n   2. A person who is judged by a medical doctor to be unable to take part in this research due to extremely poor health\n   3. A person under the age of 19","19 Years",{"count":170,"type":21},396,[24],"To test the effects of home-based care on unplanned hospitalization within 6 months among advanced cancer patients with decreased performance status. Home-based care includes education for patients and their family caregivers, home visits by specialized home-based medical staff, and regular status check-ups.",[174,31,175,176],"Malignant Neoplasm","Quality of LIfe","Unplanned Hospitalization","2022-11-23",{"date":179,"type":38},"2022-12-05",{"date":181,"type":38},"2022-07-25",{"date":183,"type":21},"2026-12-31",{"name":185,"class":45},"Seoul National University Hospital"]