[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"family-support\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:family-support":32},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,53,83,108],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":37,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100510689","evaluating-novel-healthcare-approaches-to-nurturing-and-caring-for-hospitalized-elders-100510689",false,"NCT05929703","Evaluating Novel Healthcare Approaches to Nurturing and Caring for Hospitalized Elders","Evaluating Novel Healthcare Approaches to Nurturing and Caring for Hospitalized Elders (ENHANCE)","ENHANCE","Inclusion Criteria:\n\n* Provision of informed consent\n* At least 70 years of age\n* Anticipated length of hospital stay at least 72 hours\n* Family member or care partner available to be on-site in the hospital\n* At least one delirium risk factor (e.g., cognitive or functional impairment, dehydration, vision or hearing impairment)\n* Evaluable cognitive function at baseline (i.e., ability to complete baseline cognitive function assessment)\n\nExclusion Criteria:\n\n* Delirium on admission\n* Unable to communicate verbally (e.g., coma, mechanical ventilation)\n* Unable to participate fully in interventions (e.g., terminal condition, advanced dementia)\n* Staff safety concerns (e.g., violent behavior)\n* Cardiac or intracranial surgery (due to competing causes of delirium)","ALL","70 Years",{"count":20,"type":21},1900,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical trial is to compare the Hospital Elder Life Program (HELP) with a family-augmented version of HELP (FAM-HELP), that includes family members and care partners, for the prevention of delirium in older patients during hospital admission. The main objectives of the trial are the following:\n\n1. To compare the effectiveness of FAM-HELP and HELP in reducing both the incidence of delirium and its severity.\n2. To compare the effectiveness of FAM-HELP and HELP in improving patient- and family-reported outcomes.\n3. To explore the implementation context, process, and outcomes of the FAM-HELP program in diverse hospital settings.",[27,28,29,30,31,32,33,34,35,36],"Delirium","Neurocognitive Disorders","Mild Cognitive Impairment","Alzheimer Disease","Aging","Family Support","Family Members","Caregiver Burden","Implementation Science","Patient Satisfaction",[27,38,39,35],"Clinical Trial","Comparative Effectiveness Research","RECRUITING","2026-03-20",{"date":43,"type":44},"2026-03-24","ACTUAL",{"date":46,"type":44},"2023-12-04",{"date":48,"type":21},"2027-08",{"name":50,"class":51},"University of Michigan","OTHER",7,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":4,"eligibilityCriteria":59,"healthyVolunteers":11,"sex":17,"minAge":60,"maxAge":61,"enrollmentInfo":62,"targetDuration":4,"studyType":22,"phases":64,"briefSummary":65,"conditions":66,"keywords":4,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":82},"100536179","hybrid-type-1-randomized-pilot-trial-of-a-peer-led-family-and-social-strengthening-group-intervention-for-refugee-families-100536179","NCT06261463","Hybrid Type 1 Randomized Pilot Trial of a Peer-led Family and Social Strengthening Group Intervention for Refugee Families","Leveraging Implementation Science and Design Methods to Sustain Community-based Mental Health Services for Refugees","To participate in the study, the families must meet the following criteria:\n\n1. Country of origin: Iraq, Syria, Lebanon, Jordan, Palestine or Yemen\n2. refugee family living in Chicago \\\u003C three years\n3. Contains at least one adult caregiver (18-55) and at least one of their children (age 12 and older) living in one household\n4. One family member with \\> 3 on the GHQ-12\n5. able to give written informed consent.\n\nExclusion criteria for refugee families:\n\n1. Not from one of the following Arabic-speaking countries in the Middle East: Iraq, Syria, Jordan, Lebanon, Palestine, Yemen\n2. men and women who do not have least one child aged 12 years and older living in one household\n3. arrived in the U.S as a refugee greater than 3 years ago\n4. persons with developmental disabilities which would preclude their participation in the adapted CAFES intervention\n5. persons with severe mental health (e.g., suicidality psychotic disorder), active substance use or current in family crisis (e.g., domestic violence, divorce proceedings).","12 Years","55 Years",{"count":63,"type":21},74,[24],"The proposed study draws on prior research to evaluate the feasibility, acceptability and explore preliminary effectiveness of Coffee and Family Education and Support, Version (CAFES2) using a pilot randomized type 1 hybrid effectiveness-implementation design. CAFES2 is a peer-led family and social strengthening multiple family group intervention that is designed to respond to multi-level needs of refugee families. Results of the trial will contribute to the emerging evidence base on family-based mental health interventions for refugee and newcomer communities. The trial will also generate new insights regarding implementation strategies needed to promote successful delivery of services by peer providers and the unique role of human-centered design practices for adaptation of mental health and psychosocial interventions.",[67,68,69,70,71,32,72],"Depression","Anxiety","PTSD","Family Dynamics","Social Functioning","Family Relations","2025-09-25",{"date":75,"type":44},"2025-10-01",{"date":77,"type":44},"2024-05-31",{"date":79,"type":21},"2026-08-30",{"name":81,"class":51},"University of Illinois at Chicago",1,{"id":84,"slug":85,"hasResults":11,"nctId":86,"briefTitle":87,"officialTitle":87,"acronym":4,"eligibilityCriteria":88,"healthyVolunteers":89,"sex":17,"minAge":90,"maxAge":4,"enrollmentInfo":91,"targetDuration":4,"studyType":22,"phases":93,"briefSummary":94,"conditions":95,"keywords":4,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":100,"startDateStruct":102,"completionDateStruct":104,"leadSponsor":106,"locationsCount":82},"100519127","the-family-perspectives-project-pilot-trial-100519127","NCT06039501","The Family Perspectives Project Pilot Trial","Inclusion Criteria:\n\n* Patient inclusion criteria:\n\n  * Individuals 18 years old or older.\n  * Individuals admitted to the medical intensive care unit (MICU) at Cedars-Sinai Medical Center.\n  * Individuals with acute respiratory failure, defined as \\>24 hours of invasive mechanical ventilation.\n  * Individuals who received invasive mechanical ventilation within 24 hours of admission to the MICU.\n  * Individuals expected to need invasive mechanical ventilation for \\>72 hours total, as determined by the patient's intensivist physician (fellow or attending).\n* Primary surrogate decision maker inclusion criteria:\n\n  o Individuals 18 years old or older.\n  * Individual who self-identifies as the most responsible for making decisions for the enrolled patient (can be either family member or close friend).\n  * Proficiency in English language.\n* ICU support counselor inclusion criteria:\n\n  * Individuals 18 years old or older.\n  * Individuals who work as hospital chaplains in the MICU.\n* Physician (intensivist) inclusion criteria:\n\n  * Individuals 18 years old or older.\n  * Individuals who work as critical care physicians in the MICU (fellow or attending).\n* Nurse inclusion criteria:\n\n  * Individuals 18 years old or older.\n  * Individuals who work as bedside nurses in the MICU.\n* Social worker inclusion criteria:\n\n  * Individuals 18 years old or older.\n  * Individuals work as social workers in the MICU.\n\nExclusion Criteria:\n\n* Patient exclusion criteria:\n\n  o Any records flagged \"break the glass\" or \"research opt out.\"\n\n  o Individuals expected to die within 24 hours of potential enrollment, as determined by the patient's intensivist physician (fellow or attending).\n\n  o Individuals on comfort care protocol or with clear preference for comfort care, as determined by the patient's intensivist physician (fellow or attending).\n  * Individuals who are chronically dependent on a ventilator prior to admission.\n  * Individuals with acute on chronic neuromuscular disease-related respiratory failure (e.g., Guillain Barre, Muscular Dystrophy, Myasthenia Gravis, etc.).\n  * Individuals imminently awaiting organ transplant, as determined by the patient's intensivist physician (fellow or attending).\n  * Individuals with decisional capacity, as determined by the patient's intensivist physician (fellow or attending).\n  * Individuals who are unrepresented (i.e., patient has no surrogate decision maker).\n  * Individuals whose potential enrolled family member (primary surrogate decision maker) is not proficient in English.\n  * Individuals whose attending physician is the PI on this study at the time of potential enrollment.\n  * Individuals who are cared for by intensivist physicians (fellow and attending) who do not agree to participate in the study.\n  * Individuals who have a pre-existing relationship with a hospital chaplain who does not agree to participate in the study, as determined by that chaplain.\n* Primary surrogate decision maker exclusion criteria:\n\n  o Not proficient in English language. (Rationale: materials and intervention are not adapted in other languages.)\n* ICU support counselor exclusion criteria:\n\n  o None\n* Physician (intensivist) exclusion criteria:\n\n  o None\n* Nurse exclusion criteria:\n\n  o None\n* Social worker exclusion criteria:\n\n  * None",true,"18 Years",{"count":92,"type":21},70,[24],"The purpose of the study is to conduct a pilot randomized trial of a program designed to enhance equitable communication and emotional support for families of critically ill patients in order to determine feasibility, acceptability, and participant experience with the program.\n\nThe primary study procedures include: chart abstraction, questionnaires, meetings with ICU support counselors, meetings with ICU physicians and care team, audio recordings of these meetings (optional), and interviews with study participants (optional).\n\nStudy participants include: 70 critically ill patients with acute respiratory failure (enrolled with the consent of their Legally Authorized Representative) and their primary surrogate decision makers as well as ICU support counselors and ICU care teams (physicians, nurses, social workers).",[96,32,97,98],"Respiratory Failure","Physician-Patient Relations","Critical Illness","2025-06-12",{"date":101,"type":44},"2025-06-15",{"date":103,"type":44},"2023-10-13",{"date":105,"type":21},"2026-10",{"name":107,"class":51},"Matthew Modes",{"id":109,"slug":110,"hasResults":11,"nctId":111,"briefTitle":112,"officialTitle":113,"acronym":114,"eligibilityCriteria":115,"healthyVolunteers":11,"sex":17,"minAge":116,"maxAge":117,"enrollmentInfo":118,"targetDuration":4,"studyType":22,"phases":120,"briefSummary":121,"conditions":122,"keywords":123,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":128,"lastUpdatePostDateStruct":129,"startDateStruct":131,"completionDateStruct":133,"leadSponsor":135,"locationsCount":82},"100540874","dialogical-family-guidance-postdoc-study-100540874","NCT06322511","Dialogical Family Guidance PostDoc Study","The Effectiveness of Dialogical Family Guidance in Families With a Child With Neurodevelopmental Disorders","DFG II","Inclusion Criteria:\n\n* Families with a child with clinical diagnosis within neurodevelopmental ambrella (ADHD, Tourette, Autism disorder, OCD...).\n* the child must be between 4-13 years.\n\nExclusion Criteria:\n\n* Families who do not understand finnish language (because they can not fill the questionnaires and professionals offering DFG are all finnish speaking). At least one parent needs to talk finnish.\n* Families who are not motivated to receive DFG.\n* Families who do not have a child with neurodevelopmental disorders.","4 Years","13 Years",{"count":119,"type":21},50,[24],"This new family intervention, called Dialogical Family Guidance (DFG) is developed to target family needs especially in families with a child with neurodevelopmental disorders. PhD study showed, that this intervention is functioning with this target group. Participants (families) experienced that they got information, guidance to ordinary life and that the DFG-therapists were listening to them and above all, helping with individual problems and questions. DFG include six meetings and professionals need to attend on a 3-day long education before using this intervention.",[70,72,32],[124,125,126,127],"neurodevelopmental disorders","family health","family functionality","family support","2024-03-13",{"date":130,"type":44},"2024-03-21",{"date":132,"type":44},"2024-01-02",{"date":134,"type":21},"2027-12-31",{"name":136,"class":51},"Tampere University"]