[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"caregiver-burden\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:caregiver-burden":29},{"pageToken":4,"total":5,"offset":6,"count":7,"results":8},null,69,0,25,[9,47,82,115,138,164,198,222,243,274,301,336,368,396,426,448,473,499,526,564,589,614,640,671,692],{"id":10,"slug":11,"hasResults":12,"nctId":13,"briefTitle":14,"officialTitle":15,"acronym":4,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":32,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":4},"100652748","ergonomic-and-exercise-training-in-family-caregivers-a-randomized-controlled-trial-100652748",false,"NCT07776470","Examining the Effectiveness of Ergonomics and Exercise Training in Caregivers","Examining the Effectiveness of Ergonomics and Exercise Training in Caregivers: A Randomized Controlled Trial","Inclusion Criteria\n\n* Aged 18-65 years\n* Providing care to a dependent individual for at least 6 months, at least 4 hours per day\n* Literate, with no intellectual or hearing impairment preventing communication\n* Not having participated in a regular exercise or ergonomic training programme in the previous 6 months\n* Willing to participate and provide written informed consent\n\nExclusion Criteria\n\n* Severe neurological, cardiovascular, or orthopaedic disease precluding exercise\n* Pregnancy\n* Spinal or extremity surgery within the previous 3 months",true,"ALL","30 Years","60 Years",{"count":22,"type":23},48,"ESTIMATED","INTERVENTIONAL",[26],"NA","Family and formal caregivers of partially or fully dependent individuals repeatedly perform physically demanding tasks such as lifting, transferring, repositioning, and hygiene care. These tasks increase biomechanical loading and place caregivers at high risk of musculoskeletal complaints, which in turn increase perceived caregiver burden, burnout, and fatigue. Interventions for this population have most often been limited to information leaflets or theoretical instruction, and the active exercise component has usually been absent. Furthermore, teaching safe transfer techniques alone may be insufficient when caregivers lack the muscle strength, trunk (core) stability, and flexibility required to perform those techniques.",[29,30,31],"Caregiver Burden","Caregiver Burnout","Musculoskeletal Pain",[33,34],"ergonomic","caregivers","NOT_YET_RECRUITING","2026-08-19",{"date":38,"type":39},"2026-08-21","ACTUAL",{"date":41,"type":23},"2026-08-25",{"date":43,"type":23},"2027-01-20",{"name":45,"class":46},"Uskudar University","OTHER",{"id":48,"slug":49,"hasResults":12,"nctId":50,"briefTitle":51,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":12,"sex":18,"minAge":53,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":24,"phases":56,"briefSummary":57,"conditions":58,"keywords":63,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":81},"100652450","a-mobile-informatics-solution-to-assist-caregivers-in-care-coordination-and-monitoring-social-engagement-100652450","NCT07773493","A Mobile Informatics Solution to Assist Caregivers in Care Coordination and Monitoring Social Engagement","Inclusion Criteria:\n\n* Persons with memory concerns must be English speaking.\n* Persons with memory concerns must self-report a healthcare provider visit due to memory concerns or memory related diagnosis by a physician or other qualified health care provider consistent with having mild-to-moderate memory impairment.\n* Persons with memory concerns must be over the age of 65.\n* Persons with memory concerns must be able to formally consent or assent to participate in the study.\n* Persons with memory concerns must have internet access.\n* Care partners of persons with memory concerns must speak English.\n* Care partners must be 18 years of age and over.\n* Care partners must self-identify as the primary caregiver for the person with memory concerns.\n* Care partners must indicate a willingness to use the Social Reminder System as well as to being randomized to a control group.\n* Care partners must have a mobile phone with internet access in order to install and use the care partner app.\n\nExclusion Criteria:\n\n* Those who do not meet the criteria above will be excluded.\n* Persons with memory concerns with severe or no dementia are not eligible.\n* Individuals who score below 6 and above 24 on the TICS-40 will not be eligible.","18 Years",{"count":55,"type":23},200,[26],"This study will evaluate the Social Reminder System, a mobile informatics system designed to support persons with memory concerns and their care partners. The system is intended to aid social integration for persons with memory concerns and improve care coordination and reduce caregiver burden among caregivers.\n\nResearchers will enroll 100 persons with memory concerns and their care partners. Half of the dyads will be randomly assigned to receive the Social Reminder System technology for a 6-month period, and the other half will be randomly assigned to the usual care control group. Participants will complete baseline, 3-month, and 6-month surveys. A subset of participants who receive the technology will also be asked to complete a semi-structured interview after the 6-month survey.",[59,60,61,62,29],"Memory Disorders","Mild Cognitive Impairment","Dementia","Social Isolation",[64,65,66,67,68,69,70,71,72],"Social Reminder System","SRS","Persons with memory concerns","Social engagement","Mobile health","Care coordination","Alzheimer's disease and related dementias","Mild-to-moderate memory impairment","Caregiver stress","2026-08-14",{"date":36,"type":39},{"date":76,"type":23},"2026-11-01",{"date":78,"type":23},"2028-06",{"name":80,"class":46},"University of Minnesota",1,{"id":83,"slug":84,"hasResults":12,"nctId":85,"briefTitle":86,"officialTitle":87,"acronym":88,"eligibilityCriteria":89,"healthyVolunteers":12,"sex":18,"minAge":53,"maxAge":90,"enrollmentInfo":91,"targetDuration":4,"studyType":24,"phases":93,"briefSummary":94,"conditions":95,"keywords":98,"overallStatus":105,"whyStopped":4,"lastUpdateSubmitDate":106,"lastUpdatePostDateStruct":107,"startDateStruct":109,"completionDateStruct":111,"leadSponsor":113,"locationsCount":81},"100609916","improving-self-care-of-caregivers-of-adults-in-homecare-with-heart-failure-and-cognitive-impairment-100609916","NCT07220798","Improving Self-Care of Caregivers of Adults in Homecare With Heart Failure and Cognitive Impairment","Improving Self-Care of Caregivers of Adults in Homecare With Heart Failure and Cognitive Impairment (iCare4Me Homecare)","iCare4Me HC","Inclusion Criteria:\n\n* Patient Inclusion Criteria\n\n  1. Older adults (=\\>50 years of age)\n  2. Enrolled in Home Health Care\n  3. Documented to have HF\n  4. Mild to moderate CI on the BIMS or OASIS items\n  5. Able to provide informed consent\n  6. Able to provide self-report data\n* Caregiver Inclusion Criteria\n\n  1. Adults (=\\>18 years of age)\n  2. Spouse\u002Fpartner\u002Fchild or other informal caregiver living with or in close proximity to the patient\n  3. Caregiver of a home care patient who is currently receiving or recently received services and who has mild to severe cognitive impairment\n  4. Reporting poor self-care on screening (Health Self-Care Neglect scale score =\\>2)\n  5. Reporting poor mental health on screening (screened with the PROMIS Global Mental Health 4a score \\\u003C12)\n  6. Caregiving or supporting the patient at least 8 hours\u002Fweek\n  7. Able to complete the protocol, e.g., adequate vision and hearing, English speaking.\n  8. Able to provide informed consent\n  9. Able to use technology\n\nExclusion Criteria:\n\n* Patient Exclusion Criteria\n\n  1. Dementia (ICD-10 code for dementia)\n  2. Enrolled in hospice\n  3. Non-English speaking\n* Caregiver Exclusion Criteria 1. Non-English speaking","101 Years",{"count":92,"type":23},316,[26],"This RCT design will enroll 256 informal caregivers (spouse\u002Fpartner or child) of HHC patients with HF\u002FCI and 60 patients with HF and mild to moderate CI (60 dyads). After collecting baseline data, we will block randomize the caregivers 1:1 to the ViCCY intervention or comparator group, stratifying randomization by caregiver sex (male\u002Ffemale), relationship (spouse\u002Fpartner or child), and race (white\u002Fother)- factors known to influence caregiving burden, perceived stress, and receptivity to the intervention. We will encourage caregivers to use their own devices but provide tablet devices with wireless network access if needed. The intervention group will receive 10 sessions of ViCCY over 6 months.",[96,97,29],"Heart Failure","Cognitive Impairment",[99,100,101,102,103,104],"heart failure","cognitive impairment","caregiver burden","caregiver stress","self-care","dyads","RECRUITING","2026-08-10",{"date":108,"type":39},"2026-08-12",{"date":110,"type":39},"2026-05-28",{"date":112,"type":23},"2030-04-28",{"name":114,"class":46},"Visiting Nurse Service of New York",{"id":116,"slug":117,"hasResults":12,"nctId":118,"briefTitle":119,"officialTitle":120,"acronym":121,"eligibilityCriteria":122,"healthyVolunteers":12,"sex":18,"minAge":20,"maxAge":4,"enrollmentInfo":123,"targetDuration":4,"studyType":24,"phases":125,"briefSummary":126,"conditions":127,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":130,"lastUpdatePostDateStruct":131,"startDateStruct":132,"completionDateStruct":134,"leadSponsor":136,"locationsCount":81},"100628402","penn-state-emergency-medicine-cares-care-partner-evaluation-and-sourcing-in-the-emergency-department-100628402","NCT07461168","Penn State Emergency Medicine CarES: Care-partner Evaluation and Sourcing in the Emergency Department","Penn State Emergency Medicine CarES: Care-partner Evaluation and Sourcing in the ED","CarES","Inclusion Criteria:\n\n* Person completed the CarES Observational Study.\n* Person is a care partner and:\n* Lives with the person living with dementia or\n* Checks on them at least once per week in person or by phone\n* Person is willing and able to participate in study assessments\n\nExclusion Criteria:\n\n* Person is no longer a care partner for a person living with dementia\n* Person declines participation",{"count":124,"type":23},20,[26],"Care partners of people living with dementia often experience ongoing stress and unmet support needs. This study evaluates the feasibility of a low-intensity, supportive education and resource intervention for care partners who previously participated in an observational study.\n\nParticipants complete a baseline phone interview and a short stress journaling activity, followed by a six-week series of automated educational and supportive messages delivered by text message or email. Participants may also take part in an optional peer support focus group. The study examines caregiver stress, resilience, engagement with resources, and participant feedback to inform future caregiver support interventions.",[61,128,29,129],"Caregiver Stress","Caregiver Burden of People With Dementia","2026-08-06",{"date":106,"type":39},{"date":133,"type":23},"2026-08-31",{"date":135,"type":23},"2026-12-30",{"name":137,"class":46},"Milton S. Hershey Medical Center",{"id":139,"slug":140,"hasResults":12,"nctId":141,"briefTitle":142,"officialTitle":143,"acronym":144,"eligibilityCriteria":145,"healthyVolunteers":17,"sex":18,"minAge":53,"maxAge":146,"enrollmentInfo":147,"targetDuration":4,"studyType":24,"phases":149,"briefSummary":150,"conditions":151,"keywords":4,"overallStatus":105,"whyStopped":4,"lastUpdateSubmitDate":154,"lastUpdatePostDateStruct":155,"startDateStruct":157,"completionDateStruct":159,"leadSponsor":161,"locationsCount":163},"100651299","lived-experience-narratives-in-dementia-100651299","NCT07757178","Lived Experience Narratives in Dementia","Improving the Quality of Life for People Living With Dementia and Carers: The Design and Development of a Dementia Specific Online Narrative-Based Intervention With a Feasibility Study","LEND","General Inclusion Criteria (apply across WP1-WP3)\n\n* Adults aged 18+.\n* Able to give informed consent and participate meaningfully in the required tasks.\n* Adequate communication ability in the required study language\n\nGeneral Exclusion Criteria (apply across WP1-3)\n\n* Living in a hospital or healthcare institution at the time of the study.\n* Refusal or inability to provide informed consent, or lack of capacity to consent.\n* Inability to comprehend participant information or communicate meaningfully","99 Years",{"count":148,"type":23},60,[26],"The Lived Experience Narratives in Dementia (LEND) research programme involves five work packages (WP). WP1 explores how people living with dementia use narratives and how narratives can impact them. Findings will support the development of LEND theory. WP 2-3 focus on developing the digital Online LEND Intervention, assessing its usability and acceptability, and conducting a feasibility study within NHS memory assessment and community services. Activities across the first three WPs include interviews, focus groups, user-testing sessions, engagement evaluation interviews, and a two-arm randomised feasibility trial using a range of outcome measures. Findings from this stage will inform refinement of the intervention and determine the feasibility of progressing to a future randomised controlled trial (RCT) of the Online LEND Intervention. WP4 is the Online LEND Intervention two-arm RCT. WP5 involves dissemination. The protocol for WP4 and 5 have not yet been developed and rely on results from WP1-3.",[61,152,153,29,30],"Neuro-Degenerative Disease","Alzheimer Disease","2026-08-05",{"date":156,"type":39},"2026-08-11",{"date":158,"type":39},"2025-11-17",{"date":160,"type":23},"2029-07",{"name":162,"class":46},"University of Nottingham",2,{"id":165,"slug":166,"hasResults":12,"nctId":167,"briefTitle":168,"officialTitle":169,"acronym":4,"eligibilityCriteria":170,"healthyVolunteers":12,"sex":171,"minAge":53,"maxAge":4,"enrollmentInfo":172,"targetDuration":4,"studyType":24,"phases":174,"briefSummary":175,"conditions":176,"keywords":183,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":189,"lastUpdatePostDateStruct":190,"startDateStruct":192,"completionDateStruct":194,"leadSponsor":196,"locationsCount":4},"100649938","the-effect-of-dyadic-self-care-education-provided-to-breast-cancer-patient-caregiver-dyads-on-patient-and-caregiver-outcomes-100649938","NCT07742969","The Effect of Dyadic Self-Care Education Provided to Breast Cancer Patient-Caregiver Dyads on Patient and Caregiver Outcomes","The Effect of Dyadic Self-Care Education Provided to Breast Cancer Patient-Caregiver Dyads on Patient and Caregiver Outcomes: Self-Care Behavior, Anxiety Level, and Caregiver Burden","Inclusion Criteria:\n\nPatients:\n\n* Female patients aged 18 years or older.\n* Diagnosed with stage II or III breast cancer.\n* Aware of their breast cancer diagnosis.\n* Receiving outpatient chemotherapy after mastectomy.\n* Having received at least one cycle of an EC (epirubicin-cyclophosphamide) or AC (doxorubicin-cyclophosphamide) chemotherapy regimen.\n* Able to read and write Turkish.\n* Having a primary caregiver who is willing to participate in the study.\n* Living with the primary caregiver.\n* Conscious, able to communicate effectively, and able to provide informed consent.\n* No diagnosed psychiatric disorder.\n\nPrimary Caregivers:\n\n* Aged 18 years or older.\n* Able to read and write Turkish.\n* Living with the patient.\n* Being the patient's spouse, parent, child, friend, or another relative.\n* Assuming the main responsibility for the patient's care.\n* Willing and able to cooperate and provide informed consent.\n* No diagnosed psychiatric disorder.\n\nExclusion Criteria:\n\nPatients:\n\n* Having experienced a major adverse life event within the previous 3 months, such as bereavement or divorce.\n* Admission to an intensive care unit during the study.\n* Progression of the disease to stage IV breast cancer.\n* Death or loss to follow-up.\n\nPrimary Caregivers:\n\n* Having experienced a major adverse life event within the previous 3 months, such as bereavement or divorce.\n* Deterioration in health that prevents continued participation.\n* Transfer of the primary caregiving responsibility to another person.","FEMALE",{"count":173,"type":23},156,[26],"This randomized controlled trial aims to evaluate the effect of dyadic self-care education provided to breast cancer patient-caregiver dyads receiving outpatient chemotherapy on patient self-care behaviors, anxiety levels, and caregiver anxiety levels and caregiver burden. Participants will be randomly assigned to either a dyadic self-care education intervention or routine care. Outcomes will be assessed at baseline and follow-up using validated instruments.",[177,178,179,180,181,182,29],"Breast Cancer","Caregiver","Caregiver Anxiety","Self Care","Dyadic Intervention","Education",[184,185,186,187,188,101],"breast cancer","dyadic self care","education","self care behaviour","anxiety","2026-07-31",{"date":191,"type":39},"2026-08-03",{"date":193,"type":23},"2026-08-15",{"date":195,"type":23},"2026-10-15",{"name":197,"class":46},"Ulviye Aydan NACAK",{"id":199,"slug":200,"hasResults":12,"nctId":201,"briefTitle":202,"officialTitle":203,"acronym":204,"eligibilityCriteria":205,"healthyVolunteers":12,"sex":18,"minAge":206,"maxAge":4,"enrollmentInfo":207,"targetDuration":4,"studyType":24,"phases":209,"briefSummary":210,"conditions":211,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":214,"lastUpdatePostDateStruct":215,"startDateStruct":216,"completionDateStruct":218,"leadSponsor":220,"locationsCount":81},"100649491","artificially-intelligent-robot-control-100649491","NCT07738016","Artificially Intelligent Robot Control","Asthma Under Artificially Intelligent Robot (AIR) Control: Robotic Support for Pediatric Education","AIR","Inclusion Criteria for Caregivers or Parents:\n\n* The participant must be at least 18 years old.\n* The participant must be willing and able to participate.\n* The participant can read English or Spanish and is able to fill out survey instruments by themselves or with assistance.\n* The participant cares for a child age 4-11 with asthma.\n\nInclusion Criteria for Children:\n\n* The participant must be at least 4 years old - 11 years old with asthma.\n* The child can speak English or Spanish.\n* The participant must assent to participation.\n* The participant's guardian must have consented.\n\nExclusion Criteria for Caregivers or Parents:\n\n* The participant is younger than 18 years old.\n* The participant is unwilling to participate in the study.\n* The participant is unable to complete survey instruments.\n* The participant does not care for a child with asthma who is age 4-11.\n\nExclusion Criteria for Children:\n\n* The participant is younger than 4 years old, over 11 years old, or does not have asthma.\n* The child does not speak English or Spanish.\n* The participant is unwilling to participate in the study.\n* The participant's guardian did not consent.","4 Years",{"count":208,"type":23},80,[26],"The purpose of the study is to compare the impact of standard asthma education with the standard + Artificially Intelligent Robot (AIR) Control intervention.",[212,213,29],"Asthma in Children","Artificial Intelligence","2026-07-30",{"date":191,"type":39},{"date":217,"type":23},"2026-09",{"date":219,"type":23},"2027-08-30",{"name":221,"class":46},"University of Miami",{"id":223,"slug":224,"hasResults":12,"nctId":225,"briefTitle":226,"officialTitle":227,"acronym":4,"eligibilityCriteria":228,"healthyVolunteers":17,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":229,"targetDuration":4,"studyType":24,"phases":231,"briefSummary":232,"conditions":233,"keywords":4,"overallStatus":105,"whyStopped":4,"lastUpdateSubmitDate":235,"lastUpdatePostDateStruct":236,"startDateStruct":238,"completionDateStruct":240,"leadSponsor":241,"locationsCount":81},"100649299","online-fbt-dbt-caregiver-intervention-for-caregivers-of-individuals-with-anorexia-nervosa-100649299","NCT07734779","Online FBT-DBT Caregiver Intervention for Caregivers of Individuals With Anorexia Nervosa","A Randomized Controlled Trial of an Online Family-Based Treatment (FBT) Combined With Dialectical Behavior Therapy (DBT) Intervention Versus Online Supportive Psychological Intervention for Reducing Caregiver Burden Among Caregivers of Individuals With Anorexia Nervosa","Inclusion Criteria:\n\n* Primary caregiver of an individual diagnosed with anorexia nervosa (AN) by a qualified clinician.\n\nThe individual with AN is between 10 and 18 years of age. The individual with AN does not have a severe comorbid physical illness or severe psychiatric disorder.\n\nThe caregiver lives in the same household as the individual with AN. The caregiver has at least a primary school level of education and is able to complete study procedures and questionnaires.\n\nAll participating caregivers from the same family are willing to participate in the intervention and assessment procedures.\n\nAble and willing to provide informed consent.\n\nExclusion Criteria:\n\n* Currently providing care for another family member with a chronic physical illness or psychiatric disorder.\n\nCurrent or past history of a severe physical illness or severe psychiatric disorder that would interfere with study participation.\n\nSevere emotional instability, active self-harm or suicidal behavior, psychotic symptoms, or other psychiatric conditions requiring immediate clinical intervention.\n\nUnable or unwilling to participate in the intervention or assessment procedures.",{"count":230,"type":23},100,[26],"Anorexia nervosa (AN) is a severe psychiatric disorder characterized by a chronic and relapsing course. Caregivers of individuals with AN often experience substantial caregiving burden, emotional distress, and impairment in family functioning due to their ongoing responsibilities in meal supervision, treatment support, and symptom management. Despite the critical role of caregivers in treatment and recovery, evidence-based interventions specifically targeting caregiver burden remain limited in China.\n\nThis study aims to develop and evaluate an online intervention integrating Family-Based Treatment (FBT) and Dialectical Behavior Therapy (DBT) for caregivers of individuals with AN. FBT emphasizes empowering caregivers to support nutritional rehabilitation and recovery, whereas DBT provides skills in emotion regulation, validation, and effective communication. The integration of these approaches may help caregivers reduce distress, improve caregiving skills, and enhance family functioning.\n\nThis study will employ a randomized controlled trial design. A total of 80 primary caregivers of individuals with AN will be recruited and randomly assigned to either an online FBT-DBT intervention group or an online supportive psychological intervention group. Both interventions will be delivered in a group format over 12 weeks. Assessments will be conducted at baseline, 4 weeks, 8 weeks, post-intervention (12 weeks), and at 1-month and 3-month follow-up. The primary outcome will be caregiver burden. Secondary outcomes will include psychological distress, negative emotional experiences, and the impact of eating disorder symptoms on the family.\n\nThe study aims to determine the effectiveness of the online FBT-DBT intervention in reducing caregiver burden and psychological distress and to evaluate whether it provides greater benefits than supportive psychological intervention. Findings may contribute to the development of accessible and evidence-based caregiver interventions for families affected by AN in China.",[234,29],"Anorexia Nervosa","2026-07-24",{"date":237,"type":39},"2026-07-29",{"date":239,"type":39},"2026-04-03",{"date":43,"type":23},{"name":242,"class":46},"Shanghai Mental Health Center",{"id":244,"slug":245,"hasResults":12,"nctId":246,"briefTitle":247,"officialTitle":248,"acronym":249,"eligibilityCriteria":250,"healthyVolunteers":12,"sex":18,"minAge":53,"maxAge":4,"enrollmentInfo":251,"targetDuration":4,"studyType":24,"phases":253,"briefSummary":254,"conditions":255,"keywords":258,"overallStatus":105,"whyStopped":4,"lastUpdateSubmitDate":235,"lastUpdatePostDateStruct":266,"startDateStruct":268,"completionDateStruct":270,"leadSponsor":272,"locationsCount":81},"100643619","nurse-led-caregiver-support-program-in-home-palliative-care-100643619","NCT07593729","Nurse-Led Caregiver Support Program in Home Palliative Care","Effect of a Nurse-Led Caregiver Support Program on Caregiver Competency and Healthcare Utilization Among Family Caregivers in Home Palliative Care: A Randomized Controlled Trial","CARE-PAL","Inclusion Criteria:\n\n* Adult family caregivers of patients receiving home palliative care services\n* Age 18 years or older\n* Being the primary caregiver responsible for the patient's daily care\n* Ability to communicate in Turkish\n* Willingness to participate in the study\n\nExclusion Criteria:\n\n* Professional or paid caregivers\n* Caregivers with severe cognitive impairment or severe psychiatric disorders\n* Inability to participate in follow-up assessments",{"count":252,"type":23},150,[26],"This randomized controlled trial aims to evaluate the effect of a nurse-led caregiver support program on caregiver competency and healthcare utilization among family caregivers of patients receiving home palliative care. Family caregivers in the intervention group will receive a structured 6-week nurse-led support program including face-to-face education, weekly telephone coaching, caregiver guidance materials, and decision support for symptom management and healthcare utilization. The control group will continue to receive routine home palliative care services. Primary outcome is caregiver competency. Secondary outcomes include caregiver burden, self-efficacy, patient symptom burden, emergency department visits, and hospitalizations.",[256,29,257],"Palliative Care","Home Care",[259,260,261,262,263,264,265],"Nurse-led intervention","Family caregiver","Caregiver competency","Home care","Randomized controlled trial","Palliative care","Healthcare utilization",{"date":267,"type":39},"2026-07-27",{"date":269,"type":39},"2026-05-12",{"date":271,"type":23},"2026-09-30",{"name":273,"class":46},"Kutahya Health Sciences University",{"id":275,"slug":276,"hasResults":12,"nctId":277,"briefTitle":278,"officialTitle":279,"acronym":4,"eligibilityCriteria":280,"healthyVolunteers":12,"sex":18,"minAge":53,"maxAge":4,"enrollmentInfo":281,"targetDuration":4,"studyType":24,"phases":283,"briefSummary":284,"conditions":285,"keywords":290,"overallStatus":105,"whyStopped":4,"lastUpdateSubmitDate":294,"lastUpdatePostDateStruct":295,"startDateStruct":296,"completionDateStruct":297,"leadSponsor":299,"locationsCount":81},"100648086","supporting-mental-health-and-reducing-care-stress-in-caregivers-of-persons-with-cardiovascular-disease-100648086","NCT07717723","Supporting Mental Health and Reducing Care Stress in Caregivers of Persons With Cardiovascular Disease","Supporting Mental Health and Reducing Care Stress in Caregivers of Persons With Cardiovascular Disease: A Hybrid Effectiveness-Implementation Study of Caregiving Support in Cardiac Rehabilitation","Inclusion Criteria:\n\n* 18 years of age or older\n* Is a caregiver for a patient receiving care in our UC Davis Cardiac Rehabilitation Clinic. A caregiver is defined as someone who provides support to the patient with one or more basic or instrumental activities of daily living.\n* Has one or more caregiving-related challenges or issues that they would like support with\n* Is able to read and speak in English\n\nExclusion Criteria:\n\n* Is a paid professional caregiver with no family or fictive kin relationship with the care recipient\n* Has a diagnosis of major cognitive impairment or Alzheimer's or related dementias\n* Is unable to complete the protocol or participate in the intervention (e.g., unavailable during the intervention period, unable to access or use virtual meeting technology)",{"count":282,"type":23},40,[26],"The purpose of this study is to evaluate the preliminary efficacy, feasibility, acceptability, and barriers and facilitators to implementation of the Confident Caregiver intervention among family caregivers of persons with cardiovascular disease participating in cardiac rehabilitation. Caregivers receive four individualized intervention sessions focused on assessment of caregiving challenges, tailored coaching, stress reduction, education, and referrals to supportive resources. Outcomes include reductions in caregiving-related challenges, improvements in mental health, and reductions in stress.",[29,286,287,288,289],"Stress","Depression","Anxiety","Cardiovascular Diseases",[291,292,293],"Cardiac Rehabilitation","Caregiver Support","Confident Caregiver","2026-07-23",{"date":267,"type":39},{"date":294,"type":39},{"date":298,"type":23},"2027-12",{"name":300,"class":46},"University of California, Davis",{"id":302,"slug":303,"hasResults":12,"nctId":304,"briefTitle":305,"officialTitle":306,"acronym":307,"eligibilityCriteria":308,"healthyVolunteers":12,"sex":18,"minAge":53,"maxAge":4,"enrollmentInfo":309,"targetDuration":4,"studyType":24,"phases":311,"briefSummary":312,"conditions":313,"keywords":317,"overallStatus":105,"whyStopped":4,"lastUpdateSubmitDate":327,"lastUpdatePostDateStruct":328,"startDateStruct":330,"completionDateStruct":332,"leadSponsor":334,"locationsCount":163},"100647499","nurse-led-caregiver-support-for-older-adults-with-advanced-lung-cancer-100647499","NCT07708870","Nurse-Led Caregiver Support for Older Adults With Advanced Lung Cancer","Expanding Caregiving Capacities for Caregivers of Older Adults With Newly Diagnosed Advanced Lung Cancer: A Study of Current Status and Evaluation of the Integrating Nurse-Led and Resource Utilization-Based Caregiver Support Model (ICSM)","ICSM","Inclusion Criteria:\n\nPatient inclusion criteria:\n\n* Older adults with newly diagnosed locally advanced or advanced non-small cell lung cancer.\n* Stage III or stage IV non-small cell lung cancer.\n* Aware of their cancer diagnosis.\n* Preparing to receive anti-cancer medical treatment.\n* Able to communicate verbally and complete study assessments.\n* Willing to participate in the study and provide written informed consent.\n\nCaregiver inclusion criteria:\n\n* Adult aged 18 years or older.\n* Identified by the eligible patient as the fixed primary family caregiver.\n* Able to participate in the study together with the patient as a patient-caregiver dyad.\n* Willing to participate in the study and provide written informed consent.\n\nExclusion Criteria:\n\nPatient exclusion criteria:\n\n\\- Severe cognitive impairment that prevents completion of study questionnaires or assessments.\n\nCaregiver exclusion criteria:\n\n* Unable to communicate sufficiently to complete study assessments.\n* Unable or unwilling to provide written informed consent.",{"count":310,"type":23},120,[26],"This two-phase study aims to examine the current status of older adults with newly diagnosed locally advanced or advanced non-small cell lung cancer and their primary family caregivers, and to evaluate the effects of the Integrating Nurse-Led and Resource Utilization-Based Caregiver Support Model (ICSM). Phase I is a cross-sectional correlational study assessing distress, unmet care needs, resource awareness and utilization, social support, and health promotion practice. Phase II is a two-group randomized controlled trial comparing ICSM plus oncology case manager care with oncology case manager care and usual hospital care. The intervention includes nurse-led education and counseling, symptom management, emotional coping, problem-solving, social resource use, caregiving activity arrangement, and use of a web-based or LINE-based integrated resource system.",[314,315,29,316],"Non-Small Cell Lung Cancer","Advanced Lung Cancer","Resource Utilization",[318,319,320,316,321,322,323,324,325,326],"Older Adults","Family Caregivers","Nurse-Led Intervention","Oncology Case Management","Web-Based Platform","LINE-Based Platform","Supportive Care","Psychological Distress","Quality of Life","2026-07-12",{"date":329,"type":39},"2026-07-16",{"date":331,"type":39},"2025-04-08",{"date":333,"type":23},"2027-06",{"name":335,"class":46},"National Taiwan University Hospital",{"id":337,"slug":338,"hasResults":12,"nctId":339,"briefTitle":340,"officialTitle":340,"acronym":341,"eligibilityCriteria":342,"healthyVolunteers":17,"sex":18,"minAge":53,"maxAge":343,"enrollmentInfo":344,"targetDuration":4,"studyType":24,"phases":345,"briefSummary":346,"conditions":347,"keywords":352,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":359,"lastUpdatePostDateStruct":360,"startDateStruct":362,"completionDateStruct":364,"leadSponsor":366,"locationsCount":81},"100645589","pilot-feasibility-study-of-a-dyadic-culinary-nutrition-intervention-100645589","NCT07702864","Pilot Feasibility Study of a Dyadic Culinary Nutrition Intervention","CHEF","Inclusion Criteria: Survivors\n\n* History of prostate cancer diagnosis at any stage (I-IV)\n* Identifies as Hispanic\n* Completed primary curative treatment (e.g., chemotherapy, radiation, surgery) 6 weeks prior to enrollment.\n\nNote: Men on continuing hormone therapy (ADT) or immunotherapy as maintenance or consolidation treatment are eligible. Men on active surveillance only (no treatment) are not eligible.\n\nInclusion Criterion: Caregivers\n\n* Provides unpaid support for the cancer survivor\n* No prior history of cancer (except non-melanoma skin cancer) Note: Caregivers do not need to identify as Hispanic to be eligible\n\nInclusion Criteria: Survivors and Caregivers\n\n* Aged 18-90 years\n* Reports low fruit and vegetable intake\n* Able to write, read, and speak in English or Spanish\n* Access to a mobile device with Internet and a camera\n* Co-residing and able to participate at the same time and location\n\nExclusion Criteria: Survivors and Caregivers\n\n* Cognitive difficulties that preclude answering the survey questions, that answering survey questions or participating in study activities, or providing informed consent.\n* A medical condition, movement or neurological disorder, or medication use that contraindicates participation in meal preparation.\n* Not co-residing (live in the separate households).\n* No survivor or caregiver available or willing to participate simultaneously.\n* Less than 18 years or greater than 90 years of age.","90 Years",{"count":282,"type":23},[26],"This study will determine the feasibility and acceptability of a 12-week dyadic culinary nutrition program among Hispanic prostate cancer survivor\u002Fcaregiver dyads using a randomized controlled trial design.",[348,349,350,29,351],"Neoplams","Prostate Cancer (Adenocarcinoma)","Cancer Survivors","Nutrition Therapy",[353,354,355,356,357,358],"Cancer survivorship","Caregivers","Hispanic","Men's Health","Nutrition","Pilot study","2026-07-08",{"date":361,"type":39},"2026-07-14",{"date":363,"type":23},"2027-01-01",{"date":365,"type":23},"2028-04-30",{"name":367,"class":46},"University of Arizona",{"id":369,"slug":370,"hasResults":12,"nctId":371,"briefTitle":372,"officialTitle":373,"acronym":4,"eligibilityCriteria":374,"healthyVolunteers":12,"sex":18,"minAge":53,"maxAge":4,"enrollmentInfo":375,"targetDuration":4,"studyType":24,"phases":377,"briefSummary":378,"conditions":379,"keywords":381,"overallStatus":105,"whyStopped":4,"lastUpdateSubmitDate":386,"lastUpdatePostDateStruct":387,"startDateStruct":389,"completionDateStruct":391,"leadSponsor":393,"locationsCount":395},"100557035","telephone-support-in-advanced-gastrointestinal-cancer-100557035","NCT06532877","Telephone Support in Advanced Gastrointestinal Cancer","Telephone Support Program for Patients With Advanced Gastrointestinal Cancer and Their Family Caregivers","Patient Inclusion Criteria:\n\n* Patient is at least 3 weeks post-diagnosis of unresectable stage III or stage IV gastrointestinal cancer (i.e., ampullary, anal, appendix, bile duct, colon, esophageal, gallbladder, liver, pancreatic, rectal, small intestine, or stomach cancer) and is receiving cancer care at one of the study sites.\n* Patient is at least 18 years of age.\n* Patient can speak and read English.\n* Patient has an eligible, consenting family caregiver (see criteria below).\n* Patient has moderate to severe fatigue interference with functioning.\n\nPatient Exclusion Criteria:\n\n* Patient shows significant psychiatric or cognitive impairment that would preclude providing informed consent and study participation.\n* Patient reports being able to do little activity on a functional status measure.\n* Patient is receiving hospice care at screening.\n* Patient does not have working phone service.\n* Patient has hearing impairment that precludes participation.\n* Patient participated in the pilot trial testing the same intervention.\n\nCaregiver Inclusion Criteria:\n\n* Family caregiver identified by a gastrointestinal cancer patient who meets the eligibility criteria.\n* Caregiver has significant caregiving burden.\n* Caregiver lives with the patient or has visited the patient in-person at least twice a week for the past month.\n* Caregiver is at least 18 years of age.\n* Caregiver can speak and read English.\n\nCaregiver Exclusion Criteria:\n\n* Caregiver shows significant psychiatric or cognitive impairment that would preclude providing informed consent and study participation.\n* Caregiver does not have working phone service.\n* Caregiver has hearing impairment that precludes participation.\n* Patient declines study participation.",{"count":376,"type":23},488,[26],"The goal of this clinical trial is to see if telephone support programs help patients and their family caregivers adjust to advanced gastrointestinal cancer. A new telephone counseling program that involves practicing strategies for managing stress and symptoms will be compared to a telephone program involving education on quality-of-life issues and psychosocial support. The main questions it aims to answer are:\n\nDoes our telephone counseling program lower the negative impact of patients' fatigue on their activities, emotions, and thinking abilities compared to a telephone program involving education and support? Does our telephone counseling program lower family caregivers' feelings of burden compared to a telephone program involving education and support?\n\nParticipants in both study conditions will:\n\nComplete 6 weekly telephone sessions of counseling or education\u002Fsupport Complete a telephone booster session Complete 3 telephone interviews over about 5 months",[380,29],"Gastrointestinal Neoplasm Malignant",[382,319,383,384,385,29],"Gastrointestinal Neoplasms","Acceptance and Commitment Therapy","Fatigue","Psychotherapy","2026-07-02",{"date":388,"type":39},"2026-07-06",{"date":390,"type":39},"2024-08-21",{"date":392,"type":23},"2029-02",{"name":394,"class":46},"Indiana University",4,{"id":397,"slug":398,"hasResults":12,"nctId":399,"briefTitle":400,"officialTitle":401,"acronym":4,"eligibilityCriteria":402,"healthyVolunteers":17,"sex":18,"minAge":403,"maxAge":404,"enrollmentInfo":405,"targetDuration":4,"studyType":24,"phases":407,"briefSummary":408,"conditions":409,"keywords":415,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":418,"lastUpdatePostDateStruct":419,"startDateStruct":421,"completionDateStruct":422,"leadSponsor":424,"locationsCount":81},"100638259","brief-intervention-addressing-stigma-among-parents-of-children-with-mental-health-problems-100638259","NCT07594730","Brief Intervention Addressing Stigma Among Parents of Children With Mental Health Problems","RCT of Brief Intervention Addressing Stigma Among Parents of Children With Mental Health Problems","Inclusion Criteria:\n\n* Self-identify as English Speaking\n* Live in the US\n* Ages 25-50\n* Have a child 6-18 years old with either depression, ADHD, or a substance use problem\n\nExclusion Criteria:\n\n* Do not speak English\n* Do not live in the US\n* \\\u003C25 or \\>50\n* Do not have a child between ages 6-18 with depression, ADHD, or a substance use problem","25 Years","50 Years",{"count":406,"type":23},1600,[26],"The goal of this study is to test the efficacy of brief video interventions parental internalized stigma and stigma-related outcomes (e.g., treatment intentions, caregiver burden, secrecy) among parents (ages 25-50) of children ages 6-18 with depression, ADHD, or substance use problems.\n\nTimely identification and treatment of mental health problems in youth is a public health priority. However, many youth do not receive treatment, and stigma has been identified as the primary barrier to help-seeking. Parents experience stigma related to their children having mental health problems, which has been associated with reduced help-seeking and increased parental distress. Prior experiments have found brief video-based interventions (BVIs), 1-2 minute videos similar to those viewed by youth on social media platforms, based on the principle of \"social contact\" with individuals affected by a stigmatized condition, effective in reducing mental health stigma and increasing help-seeking.\n\nIn this 4-arm RCT, the investigators will recruit parents aged 25-50 using an online crowdsourcing platform, to test the efficacy of BVIs featuring a personal parent narrative of their experience with their child's a) depression, b) ADHD, or c) substance use, or d) a control condition that provides general written psychoeducational information without social contact.",[410,411,412,413,414,29],"Depression Disorders","ADHD","Substance Abuse","Social Stigma","Help-Seeking Behavior",[416,417,101],"social stigma","help-seeking behavior","2026-06-26",{"date":420,"type":39},"2026-06-30",{"date":388,"type":23},{"date":423,"type":23},"2026-09-06",{"name":425,"class":46},"New York State Psychiatric Institute",{"id":427,"slug":428,"hasResults":12,"nctId":429,"briefTitle":430,"officialTitle":431,"acronym":432,"eligibilityCriteria":433,"healthyVolunteers":12,"sex":18,"minAge":53,"maxAge":4,"enrollmentInfo":434,"targetDuration":4,"studyType":24,"phases":436,"briefSummary":437,"conditions":438,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":440,"lastUpdatePostDateStruct":441,"startDateStruct":442,"completionDateStruct":444,"leadSponsor":446,"locationsCount":4},"100644580","care-burden-and-qualty-of-lfe-100644580","NCT07672340","Care Burden And Qualıty of Lıfe","Effect Of Multıdımensıonal Traınıng Applıed to Caregıvers of Home Health Servıce Recıpıents Aged 65 And Over on Care Burden And Qualıty of Lıfe","Care Burden","Inclusion Criteria:\n\nBe willing to participate in the study\n\n* Be literate\n* Have registered with a home health care unit\n* Have been responsible for the care of a relative aged 65 or older for at least one month\n* Score at least 21 on the Zarit Caregiver Burden Scale\n\nExclusion Criteria:\n\n* • Having severe reading comprehension difficulties\n\n  * Having severe hearing difficulties\n  * Having been diagnosed with a psychiatric disorder (schizophrenia, bipolar disorder, or anxiety disorder)\n  * Failing to complete the data collection instruments used in the study\n  * Failing to attend at least two training sessions",{"count":435,"type":23},78,[26],"This randomized controlled trial will be conducted to examine the effect of a multidimensional training program, to be implemented by a public health nurse, on the care burden and quality of life of primary caregivers of patients aged 65 and older.",[29,326,439],"Public Health","2026-06-24",{"date":418,"type":39},{"date":443,"type":23},"2026-07",{"date":445,"type":23},"2026-08",{"name":447,"class":46},"Aydin Adnan Menderes University",{"id":449,"slug":450,"hasResults":12,"nctId":451,"briefTitle":452,"officialTitle":453,"acronym":4,"eligibilityCriteria":454,"healthyVolunteers":17,"sex":18,"minAge":53,"maxAge":4,"enrollmentInfo":455,"targetDuration":4,"studyType":457,"phases":4,"briefSummary":458,"conditions":459,"keywords":463,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":465,"lastUpdatePostDateStruct":466,"startDateStruct":467,"completionDateStruct":469,"leadSponsor":471,"locationsCount":4},"100644131","burden-of-care-and-health-literacy-of-caregivers-in-the-emergency-department-100644131","NCT07666373","Burden of Care and Health Literacy of Caregivers in the Emergency Department","The Relationship Between Caregiver Burden and Health Literacy Among Caregivers of Patients With Chronic Diseases Presenting to the Emergency Department","The patient having visited the Yalova Training and Research Hospital Emergency Department.\n\nBeing at least 18 years of age. Being cognitively capable of answering the data collection tools (scales\u002Fquestionnaires).\n\nVolunteering to participate in the study and providing informed consent.\n\nExclusion Criteria:\n\nRefusal to participate in the research voluntarily. Not being the primary caregiver for the patient. Inability to communicate or complete the scales due to cognitive or language barriers.\n\n\\-",{"count":456,"type":23},350,"OBSERVATIONAL","This study aims to investigate the relationship between caregiver burden and health literacy among primary caregivers of patients with chronic diseases presenting to the emergency department. The study will be conducted in the Emergency Department of Yalova Training and Research Hospital and will include at least 300 caregivers. Data will be collected using a sociodemographic questionnaire, the Turkish Health Literacy Scale-32 (THLS-32), and the Zarit Burden Interview (ZBI). The findings are expected to contribute to a better understanding of caregivers' needs and to clarify the role of health literacy in caregiver burden among those providing care for individuals with chronic illnesses.",[29,460,461,462],"Health Literacy","Chronic Disease","Emergency Service Utilization",[29,460,319,464],"Emergency Service","2026-06-18",{"date":440,"type":39},{"date":468,"type":23},"2026-07-01",{"date":470,"type":23},"2027-05-31",{"name":472,"class":46},"University of Yalova",{"id":474,"slug":475,"hasResults":12,"nctId":476,"briefTitle":477,"officialTitle":478,"acronym":479,"eligibilityCriteria":480,"healthyVolunteers":12,"sex":18,"minAge":53,"maxAge":4,"enrollmentInfo":481,"targetDuration":4,"studyType":24,"phases":483,"briefSummary":484,"conditions":485,"keywords":489,"overallStatus":105,"whyStopped":4,"lastUpdateSubmitDate":490,"lastUpdatePostDateStruct":491,"startDateStruct":493,"completionDateStruct":495,"leadSponsor":497,"locationsCount":81},"100501644","the-snap-tool-for-head-and-neck-cancer-survivor-caregiver-dyads-100501644","NCT05811936","The SNAP Tool for Head and Neck Cancer Survivor-Caregiver Dyads","A Randomized Controlled Trial to Evaluate the Survivorship Needs Assessment Planning (SNAP) Tool for Head and Neck Cancer Survivor-Caregiver Dyads","SNAP","Patient Inclusion Criteria:\n\n1. Age \\>18\n2. Stage I-IV non-metastatic HNC (i.e., lip\u002Foral cavity, nasopharynx, salivary gland, oropharynx, hypopharynx, paranasal sinus, larynx and cutaneous cancers)\n3. Currently receiving radiation treatment (with\u002Fwithout surgery and\u002For concurrent chemotherapy) with curative intent\n4. Able to nominate caregiver, the primary support person, also interested in participating\n\nCaregiver Inclusion Criteria:\n\n1. Age \\>18\n2. Provide care for a loved one with stage I-IV HNC\n3. Agrees to participate after being nominated\n\nPatient Exclusion Criteria:\n\n1. Patients who do not read\u002Funderstand English\n2. Patients who are cognitively impaired and cannot complete interviews as judged by the referring health care provider\n3. Patients concurrently diagnosed with and\u002For receiving treatment for a second \"significant\" primary cancer, except the following:\n\n   * Excised and cured non-melanoma skin cancer\n   * Carcinoma in situ of breast or cervix\n   * Superficial bladder cancer\n   * Stage 1 differentiated thyroid cancer that is resected or observed\n   * pT1a\u002FpT1b prostate cancer comprising \\\u003C5% of resected tissue with normal prostate specific antigen (PSA) since resection\n   * cT1a\u002FcT1b prostate cancer treated with brachytherapy\n\nCaregiver Exclusion Criteria:\n\n1. Inability to read or understand English\n2. Cognitively impaired and cannot complete interviews, as judged by the referring health care provider",{"count":482,"type":23},352,[26],"In this randomized behavioral intervention, head and neck cancer (HNC) survivors and their caregivers (N=176 HNC survivor-caregiver dyads) will be randomized to either Survivorship Needs Assessment Planning (SNAP) or Usual Care (UC) groups to examine the effects of SNAP on outcomes. SNAP includes two sessions with a needs assessment and tailored care plan and a supportive mobile app after completion of radiation to promote uptake of recommended medical and supportive care. The study aims to evaluate the effects of SNAP on symptom severity in patients and caregiver burden in caregivers. Secondary outcomes include psychological distress (anxiety and depression), healthcare utilization (receipt of recommended care) and unmet needs and self-efficacy in HNC survivor-caregiver dyads. Participants will complete surveys at baseline, 6 months, and 9 months post randomization with validated PROMs, and receive intervention modules at the end of radiation and month 3. Participants in the SNAP group will also receive mobile app support.",[486,487,29,488],"Head and Neck Cancer","Survivorship","Head and Neck Neoplasms",[486,487],"2026-06-09",{"date":492,"type":39},"2026-06-11",{"date":494,"type":39},"2023-08-23",{"date":496,"type":23},"2027-12-31",{"name":498,"class":46},"Medical University of South Carolina",{"id":500,"slug":501,"hasResults":12,"nctId":502,"briefTitle":503,"officialTitle":504,"acronym":505,"eligibilityCriteria":506,"healthyVolunteers":17,"sex":18,"minAge":53,"maxAge":4,"enrollmentInfo":507,"targetDuration":4,"studyType":24,"phases":509,"briefSummary":510,"conditions":511,"keywords":515,"overallStatus":105,"whyStopped":4,"lastUpdateSubmitDate":518,"lastUpdatePostDateStruct":519,"startDateStruct":520,"completionDateStruct":521,"leadSponsor":523,"locationsCount":525},"100596131","psychoeducation-program-for-family-caregivers-coordinated-by-an-aprn-100596131","NCT07041463","Psychoeducation Program for Family Caregivers Coordinated by an APRN","Impact of a New Psychoeducation Program Coordinated by an Advanced Practce Nurse on the Burden of Family Caregivers of Patients With a First Pyschotic Episode.","APIPEP","Inclusion Criteria:\n\n* Caregiver relative of a patient under the care of the FEP team and meeting the criteria of international recommendations of FEP diagnosis made by the specialized team of less than 6 months, between 18 and 35 years of age.\n* Caregiver having received information about the study and having giveń consent.\n* Caregiver covered by a health insurance plan\n\nExclusion Criteria:\n\n* Caregiver under curatorship, guardianship, safeguard of justice, family habilitation or future protection mandate\n* Caregiver participating in another study that may interact with this one\n* Caregiver not fluent in French (comprehension\u002Freading)\n* Caregiver who has already received psycho-education on FEP\n* Patient's opposition to caregiver's participation in research",{"count":508,"type":23},180,[26],"The aim of this study is to assess the impact of implementing a specific family program coordinated by APRNs, covering the 5 levels of the family care pyramid through a consultation, an individual psychoeducation program and a group psychoeducation program, on improving caregiver burden and thus contributing to the recovery of users suffering from FEP.\n\nDetailed Description: Psychotic disorders are among the most disabling chronic pathologies in psychiatry. These disorders modify the individual's perceptions, thoughts, moods, behaviours and day-to-day functioning (Implementing interventions as early as possible in the first psychotic episode (FEP) would be likely to decrease the severity and consequences of the illness and improve prospects for recovery. Evidence supports the establishment of multidisciplinary teams to detect early and treat early those experiencing FEP and those at increased risk of psychosis. Recommended interventions include cognitive-behavioral therapies, family interventions, employment and educational support, and above all, at the heart of the system, case management. These specialized teams need to be multidisciplinary, bringing together psychiatrists, psychologists and social workers in addition to case managers. More recently in France, Advanced practice nurse (APRN) have joined these teams. But getting young people to accept both disorders and care is a difficult necessity, and remains a major challenge. Poor compliance with treatment is said to be one of the primary causes of relapse after FEP. Factors that increase the risk of relapse include initially more severe symptoms, persistent substance abuse, poor adherence to treatment and inadequate support from family and friends. Nowadays, support from a close caregiver for a person living with a psychic disorder is recognized as a very favorable factor for long-term prognosis. But the occurrence of a FEP often has the effect of a tidal wave for loved ones, who present high levels of psychological distress and feelings of burden. Unfortunately, it is still difficult for families to gain access to family caregiver support services, which are still insufficiently available and often unknown to them. A number of barriers stand in the way of systematically proposing family interventions, such as health professionals' lack of awareness of the effectiveness of interventions aimed at family carers, their difficulty in establishing a double therapeutic alliance with the young person and his or her family, or the misperception that family interventions are in contradiction with professional secrecy.\n\nThe pyramid of family care in early intervention presents the family support that should be available to families of young people with FEP. The levels of intervention are designed to meet the support needs of family caregivers and can be used flexibly depending on specific needs or the phase of the psychotic episode. Also, APRNs could contribute to the success of these caregiver support programs thanks to their skills in prevention, assessment and coordination of complex pathways. This study therefore aims to determine the extent to which a specific program coordinated by APRNs can influence the burden of a family caregiver of a young person suffering from FEP.",[512,29,513,514],"First Episode Psychosis (FEP)","Nurse Practitioners","IMPACT OF A NEW PSYCHOEDUCATION PROGRAM COORDINATED BY AN ADVANCED PRACTICE NURSE ON THE BURDEN OF FAMILY CAREGIVERS OF PATIENTS WITH A FIRST PSYCHOTIC EPISODE",[512,516,517],"Caregiver burden","Advanced Practice Nurse","2026-06-05",{"date":490,"type":39},{"date":518,"type":39},{"date":522,"type":23},"2030-11-04",{"name":524,"class":46},"Hôpital le Vinatier",5,{"id":527,"slug":528,"hasResults":12,"nctId":529,"briefTitle":530,"officialTitle":531,"acronym":532,"eligibilityCriteria":533,"healthyVolunteers":12,"sex":18,"minAge":53,"maxAge":4,"enrollmentInfo":534,"targetDuration":4,"studyType":24,"phases":536,"briefSummary":537,"conditions":538,"keywords":541,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":556,"lastUpdatePostDateStruct":557,"startDateStruct":558,"completionDateStruct":560,"leadSponsor":562,"locationsCount":81},"100643231","vocale-lbd-online-peer-support-for-caregivers-of-people-with-lewy-body-dementia-100643231","NCT07637097","VOCALE LBD: Online Peer Support for Caregivers of People With Lewy Body Dementia","Reducing Depression in Family Caregivers of Persons Living With Lewy Body Dementia Through Tailored Asynchronous Online Intervention.","VOCALE LBD","Inclusion Criteria:\n\n* Current family member or informal (unpaid) caregiver of a person with a confirmed diagnosis of Lewy Body Dementia (LBD) or LBD mixed pathology\n* Experiences depressive symptoms as defined by a score of 5 or higher on the Patient Health Questionnaire-9 (PHQ-9)\n* Able to read, write, and speak English\n* Has access to a device (computer, tablet, or smartphone) that can connect to the internet and be used for videoconferencing or phone calls, OR is interested in using a loaner device\n\nExclusion Criteria:\n\n* Active suicidal ideation as indicated by endorsement of PHQ-9 Item 9 (thoughts that you would be better off dead, or thoughts of hurting yourself)\n* Paid or professional caregiver (must be unpaid family\u002Finformal caregiver)\n* Unable to read, write, or speak English",{"count":535,"type":23},220,[26],"This study tests whether a tailored, fully asynchronous online group intervention (VOCALE LBD) reduces depression in family caregivers of people with Lewy Body Dementia (LBD), compared to standard educational materials. LBD is the second most common form of degenerative dementia and causes distinct challenges, including visual hallucinations, REM sleep disorder, and severe motor symptoms, that are not addressed by generic caregiver interventions. Depression rates in LBD caregivers reach 40-50%, double the rate seen in Alzheimer's disease caregivers, yet no rigorous digital interventions exist specifically for this population. VOCALE LBD is a text-based, low-bandwidth platform (Discourse) that brings groups of 10-15 caregivers together in an 8-week moderated online community. Weekly topics address LBD-specific challenges (sleep problems, hallucinations, self-care) and problem-solving skills using the ADAPT method. A pilot study (n=54) showed strong effects on depressive symptoms (Cohen's d=0.54 at 1-month follow-up), near-perfect engagement, and high participant satisfaction. This RCT (N=220) will test efficacy, examine mechanisms of action (self-efficacy and problem-solving), and explore analytics approaches for pragmatic monitoring, laying groundwork for future implementation in clinics and community organizations.",[539,540,29,354],"Lewy Bodies Disease","Depression Disorder",[542,543,544,545,546,547,548,549,550,551,552,553,554,555],"Lewy body disease","LBD","Family caregivers","Caregiver Depression","Online Intervention","Asynchronous","Digital Health","Peer Support","Problem-solving therapy","VOCALE","Telehealth","Dementia caregiver","ADAPT method","Discourse Platform","2026-06-03",{"date":490,"type":39},{"date":559,"type":23},"2026-12-01",{"date":561,"type":23},"2030-11-30",{"name":563,"class":46},"University of Washington",{"id":565,"slug":566,"hasResults":12,"nctId":567,"briefTitle":568,"officialTitle":569,"acronym":570,"eligibilityCriteria":571,"healthyVolunteers":17,"sex":18,"minAge":53,"maxAge":4,"enrollmentInfo":572,"targetDuration":4,"studyType":24,"phases":573,"briefSummary":574,"conditions":575,"keywords":578,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":581,"lastUpdatePostDateStruct":582,"startDateStruct":584,"completionDateStruct":585,"leadSponsor":587,"locationsCount":81},"100640320","tiva-mobile-health-intervention-for-family-caregivers-100640320","NCT07616284","TIVA Mobile Health Intervention for Family Caregivers","A Mobile Health Intervention for the Promotion of Mental Health in Family Caregivers: Protocol for a Pilot Study","TIVA-Pilot","Inclusion Criteria:\n\n* Adults aged 18 years or older.\n* Unpaid family caregivers of a person with chronic illness, disability, or dependency.\n* Providing regular caregiving assistance for at least 4 months.\n* Living in Portugal.\n* Ability to read and understand Portuguese.\n* Ownership and use of a smartphone with internet access compatible with the TIVA mobile application.\n* Willingness to install and use the TIVA app for 4 weeks.\n* Ability to provide informed consent.\n\nExclusion Criteria:\n\n* Severe cognitive impairment.\n* difficulties preventing independent use of the application or completion of study assessments.\n* Severe psychiatric disorder or acute mental health crisis interfering with participation.\n* Participation in another structured caregiver support or psychological intervention during the study period.\n* Inability to use a smartphone independently.",{"count":208,"type":23},[26],"This pilot study aims to evaluate the feasibility, usability, and preliminary effects of the TIVA mobile health intervention in promoting positive mental health among family caregivers of older adults. TIVA is a culturally adapted mobile application based on Lluch's Positive Mental Health model and designed to support caregivers through daily activities, motivational messages, relaxation strategies, and psychoeducational content over a four-week intervention period.\n\nA pilot randomized controlled study with parallel allocation will be conducted involving family caregivers recruited in community and primary healthcare settings in Portugal. Participants will be allocated either to the TIVA intervention group or to a usual care control group. Outcomes will include positive mental health, caregiver burden, usability, satisfaction, adherence, and acceptability. Data will be collected at baseline, post-intervention, and follow-up.\n\nThis study intends to contribute to the development of accessible digital mental health strategies to support family caregivers and promote healthy ageing.",[576,319,577,29],"Positive Mental Health","Mental Health Promotion",[579,319,576,318,577,580,29],"TIVA mHealth","Mobile Application","2026-05-29",{"date":583,"type":39},"2026-06-01",{"date":217,"type":23},{"date":586,"type":23},"2027-04",{"name":588,"class":46},"Universidade do Porto",{"id":590,"slug":591,"hasResults":12,"nctId":592,"briefTitle":593,"officialTitle":594,"acronym":4,"eligibilityCriteria":595,"healthyVolunteers":17,"sex":18,"minAge":53,"maxAge":4,"enrollmentInfo":596,"targetDuration":4,"studyType":24,"phases":597,"briefSummary":598,"conditions":599,"keywords":601,"overallStatus":105,"whyStopped":4,"lastUpdateSubmitDate":604,"lastUpdatePostDateStruct":605,"startDateStruct":607,"completionDateStruct":609,"leadSponsor":611,"locationsCount":613},"100539722","a-study-of-meaning-centered-psychotherapy-for-caregivers-to-people-with-cancer-100539722","NCT06307535","A Study of Meaning-Centered Psychotherapy for Caregivers to People With Cancer","Meaning-Centered Psychotherapy to Meet Palliative Care Needs of Cancer Caregivers","Inclusion Criteria:\n\n* Age 18 or over;\n* As per self-report, a current caregiver to a patient with Stage III or IV solid tumor cancer currently receiving medical care of any kind (e.g., curative, palliative);\n* Experiences distress as evidenced by a score of 4 or greater on the Distress Thermometer (DT) and an indication that this distress is associated with caregiving;\n* As per self-report, can read and understand English;\n* As per self-report, residing in New York, New Jersey, Connecticut, or Florida, or have the ability to complete sessions while complying with current telehealth regulations.\n\nExclusion Criteria:\n\n* Participant does not have a reasonable understanding of the study activities by the judgment of the consenting professional;\n* Engagement in regular individual psychotherapeutic support that the participant is unable or unwilling to put on hold for the course of treatment.",{"count":55,"type":23},[26],"Participants will complete 1 set of questionnaires about 2 weeks before beginning their Meaning-Centered Psychotherapy for Caregivers\u002FMCP-C or standard Supportive Psychotherapy for Caregivers\u002FSP-C sessions. These questionnaires will ask about participants' sense of meaning and purpose in life, spiritual well-being, depression and\u002For anxiety, and social support. Participants will then be assigned to receive either MCP-C or SP-C for 7 sessions. Participants will complete additional sets of questionnaires about 2 weeks, 6 months, and 12 months after their last session of MCP-C or SP-C. It will take between 35 and 50 minutes to complete each set of questionnaires.\n\nAfter participants complete the MCP-C or SP-C sessions and all 4 sets of questionnaires, their participation in this study will end. If participants decide not to complete all 7 sessions, they may still choose to complete the questionnaires.\n\nParticipants may remain in the study and continue to receive all 7 sessions of MCP-C or SP-C even if their loved one passes away.",[29,30,600],"Caregiver Stress Syndrome",[178,600,29,30,602,603],"Meaning-Centered Psychotherapy","23-376","2026-05-21",{"date":606,"type":39},"2026-05-26",{"date":608,"type":39},"2024-03-13",{"date":610,"type":23},"2029-03-01",{"name":612,"class":46},"Icahn School of Medicine at Mount Sinai",8,{"id":615,"slug":616,"hasResults":12,"nctId":617,"briefTitle":618,"officialTitle":618,"acronym":619,"eligibilityCriteria":620,"healthyVolunteers":17,"sex":18,"minAge":621,"maxAge":4,"enrollmentInfo":622,"targetDuration":4,"studyType":24,"phases":623,"briefSummary":624,"conditions":625,"keywords":627,"overallStatus":105,"whyStopped":4,"lastUpdateSubmitDate":631,"lastUpdatePostDateStruct":632,"startDateStruct":634,"completionDateStruct":636,"leadSponsor":638,"locationsCount":81},"100456159","caregiver-stress-and-sleep-study-100456159","NCT05219955","Caregiver Stress and Sleep Study","CARES","Inclusion Criteria:\n\n* Age 55 years or older.\n* Provide at least 15 hours\u002Fweek of unpaid care to a patient with a dementia diagnosis.\n* Reporting stress or strain delivering care\n* No or stable pharmacotherapy for depression\n* Meets screening definition for having morning activation difficulty or a definite morning type per the Composite Morningness Questionnaire (CMQ)\n\nExclusion Criteria:\n\n* Unsafe or unable to undergo MRI\n* Active Cognitive Behavioral Therapy for mood or insomnia\n* Probable dementia diagnosis\n* Deadly illness or plans to leave the study area\n* Current active substance use disorder","55 Years",{"count":310,"type":23},[26],"The purpose of this research study is to better understand how stress, sleep and activity might impact caregivers' mood and brain health. This study includes a randomized experimental component where therapists will systematically deliver one of two evidence-based talk-therapy treatments. The aim is to evaluate effects on meaningful health-relevant measures including morning activation levels, depression symptoms, rumination, and aspects brain connectivity previously linked with depression. Participants will complete surveys about their caregiving experiences, health, and mood, undergo an MRI, and wear an actigraphy watch that measures activity levels throughout the day and when sleeping.",[626,29],"Depressive Symptoms",[287,628,629,630],"Caregiving","Late-Life","Morningness","2026-05-15",{"date":633,"type":39},"2026-05-19",{"date":635,"type":39},"2022-07-15",{"date":637,"type":23},"2027-06-30",{"name":639,"class":46},"University of Pittsburgh",{"id":641,"slug":642,"hasResults":12,"nctId":643,"briefTitle":644,"officialTitle":645,"acronym":4,"eligibilityCriteria":646,"healthyVolunteers":12,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":647,"targetDuration":4,"studyType":24,"phases":649,"briefSummary":650,"conditions":651,"keywords":658,"overallStatus":105,"whyStopped":4,"lastUpdateSubmitDate":662,"lastUpdatePostDateStruct":663,"startDateStruct":665,"completionDateStruct":667,"leadSponsor":669,"locationsCount":81},"100605888","ai-based-personalized-health-and-self-care-100605888","NCT07168382","AI-Based Personalized Health and Self-Care","AI-Based Personalized Health and Self-Care: Investigating A Mobile Virtual Assistant to Address Health-Related Social Needs","Inclusion Criteria (Caregivers):\n\n* Must be a caregiver of a child seen within the NCH primary care network who self-identifies with at least one unmet social need\n* Must be 18 years of age or older\n* Must be English-speaking\n* Must have a device that connects to the internet\n\nInclusion Criteria (Primary Care Providers and Support Team Members):\n\n* Must be 18 years or older\n* Must be employed at Nationwide Children's Hospital\n\nExclusion Criteria:\n\n\\- Due to the intervention only being translated into English, non-English Speakers will be excluded from this study.",{"count":648,"type":23},70,[26],"The goal of this clinical trial is to learn if the DAPHNE chatbot can improve caregiver engagement, usability, and integration of social care support tools into clinical workflows in caregivers of pediatric patients receiving care at the Nationwide Children's Hospital Primary Care Center (NCH PCC). This is a pilot randomized clinical trial.\n\nThe main questions it aims to answer are:\n\n* Is the DAPHNE chatbot usable, acceptable, and minimally burdensome for caregivers over a 6-month period?\n* Can the DAPHNE chatbot be effectively integrated into primary care provider workflows?\n\nResearchers will compare the DAPHNE chatbot intervention arm to the standard of care control arm to see if the intervention improves caregiver-reported outcomes and provider workflow integration.\n\nParticipants that are patients will be randomly assigned to either the DAPHNE chatbot group or the standard of care group. Complete surveys assessing usability, acceptability, and burden and participate in brief qualitative interviews to share feedback on their experience.\n\nParticipants that are Primary Care providers will discuss integration of DAPHNE into clinical workflows and complete workflow integration assessments.",[652,653,654,655,29,656,657],"Social Needs Status","Unmet Health-Related Social Needs and Access to Community Resources","Primary Health Care and Access to Primary Care","Technology Use to Support Caregivers","Health Status, Child and Infant Care","Preventative Care Services",[659,660,661],"Social Needs","Chatbot","Community Resources","2026-05-06",{"date":664,"type":39},"2026-05-11",{"date":666,"type":39},"2026-04-24",{"date":668,"type":23},"2028-08",{"name":670,"class":46},"Emre Sezgin",{"id":672,"slug":673,"hasResults":12,"nctId":674,"briefTitle":675,"officialTitle":676,"acronym":4,"eligibilityCriteria":677,"healthyVolunteers":17,"sex":18,"minAge":20,"maxAge":4,"enrollmentInfo":678,"targetDuration":4,"studyType":457,"phases":4,"briefSummary":680,"conditions":681,"keywords":4,"overallStatus":105,"whyStopped":4,"lastUpdateSubmitDate":662,"lastUpdatePostDateStruct":684,"startDateStruct":686,"completionDateStruct":688,"leadSponsor":690,"locationsCount":81},"100568198","swallowing-impairments-in-adults-with-and-without-alzheimers-disease-100568198","NCT06678100","Swallowing Impairments in Adults With and Without Alzheimer's Disease","Prevalence and Care Partner Burden of Individuals With Alzheimer's Disease","Inclusion criteria for AD cohort:\n\n1. adult ≥60 years old\n2. diagnosis of AD by a neurologist (confirmed with imaging, spinal tap, behavioral testing)\n3. no prior history of other neurological diseases (aside from stroke which has resolved with no current symptoms)\n4. no prior history of respiratory diseases\n5. no prior history of head and neck surgery\u002Fhead and neck cancer\u002Fradiation to head and neck region\n6. consuming some form of oral intake\n7. able to follow basic directions\n8. able\u002Fwilling to provide consent\u002Fassent.\n\nExclusion Criteria for AD Cohort:\n\n1. individual \\\u003C60 years old\n2. Diagnosis of another type of dementia\n3. History of neurological\u002Frespiratory diseases\n4. History of head and neck surgery\u002Fhead and neck cancer\u002Fradiation to head and neck region\n5. not consuming any oral intake\n6. Unable to follow basic directions\n7. Unable to provide consent based on the University of California, San Diego Brief Assessment of Capacity to Consent (UBACC), score \\\u003C15 OR provide assent and a legal guardian\u002Fhealth care decision maker provides consent.\n\nInclusion criteria for care partners of individuals with AD will be:\n\n1. care partner of an individual with AD\n2. willing to complete questionnaires\u002Fparticipate in an interview.\n\nExclusion Criteria for Caregivers of Individuals with AD:\n\n1. not the primary caregiver of an individual with AD\n2. unwilling to complete questionnaires\u002Fsemi-structured interview\n\nInclusion criteria for community-dwelling adults will be:\n\n1. adult ≥60 years old\n2. no prior history of neurological diseases (aside from stroke which has resolved with no current symptoms)\n3. no prior history of respiratory diseases\n\n3\\) no prior history of head and neck surgery\u002Fhead and neck cancer\u002Fradiation to head and neck region 4) no prior history of swallowing difficulties based on participant report. 5) Score ≥25th percentile based on sex\u002Fage\u002Feducation\u002Frace on the Montreal Cognitive Assessment (MOCA)\n\nExclusion Criteria for Healthy Cohort:\n\n1. individual \\\u003C60 years old\n2. history of neurological disease\n3. history of respiratory disease\n4. history of head and neck surgery\u002Fhead and neck cancer\u002Fradiation to head and neck region\n5. history of swallowing difficulties\n6. Score \\\u003C25th percentile based on sex\u002Fage\u002Feducation\u002Frace on the Montreal Cognitive Assessment (MOCA)",{"count":679,"type":23},240,"This research study is investigating whether people with Alzheimer's disease (AD) experience more changes to swallowing than their healthy age-matched peers. The prevalence of swallowing impairments in moderate-severe AD is high (85-93%), yet little is known about how swallow function evolves throughout the disease course in people with AD. The overall objective of this study is to evaluate swallowing function in adults with and without Alzheimer's disease. The investigator will also be involving the primary caregivers of individuals with Alzheimer's that are enrolled in the study to better understand the impact of swallowing impairments on the primary caregivers of those with Alzheimer's Disease.\n\nHealthy adults and individuals with Alzheimer's disease will:\n\n* undergo tests of cough and swallow function\n* undergo tests of grip and tongue strength\n* complete questionnaires\n\nCaregivers of individuals with Alzheimer's disease will also complete questionnaires.",[153,29,682,683],"Healthy Aging","Dysphagia",{"date":685,"type":39},"2026-05-08",{"date":687,"type":39},"2025-04-21",{"date":689,"type":23},"2028-02",{"name":691,"class":46},"Vanderbilt University Medical Center",{"id":693,"slug":694,"hasResults":12,"nctId":695,"briefTitle":696,"officialTitle":697,"acronym":4,"eligibilityCriteria":698,"healthyVolunteers":17,"sex":18,"minAge":699,"maxAge":4,"enrollmentInfo":700,"targetDuration":4,"studyType":24,"phases":702,"briefSummary":703,"conditions":704,"keywords":4,"overallStatus":105,"whyStopped":4,"lastUpdateSubmitDate":715,"lastUpdatePostDateStruct":716,"startDateStruct":718,"completionDateStruct":720,"leadSponsor":722,"locationsCount":81},"100633559","act-group-for-family-caregivers-of-stroke-survivors-100633559","NCT07528261","ACT Group for Family Caregivers of Stroke Survivors","Effects of Acceptance and Commitment Therapy (ACT) Group for Family Caregivers of Stroke Survivors","Inclusion Criteria:\n\n* Age 40 or above.\n* Taking the primary responsibility for the care of a family member suffering from stroke (i.e. spending at least 70% of the time on performing caregiving tasks).\n* The stroke patient has been discharged from hospital and is currently living with the caregiver.\n* Having cared for the stroke patient for at least six months, including at least two months after discharge.\n* CSAQ score (as determied during pre-group screening meeting) indicates a high level of distress, as evidenced by one of the following: a) participant answered \"Yes\" to either or both questions 4 and 11; b) total \"Yes\" scores = 10 or more; c) score on question 17 is 6 or higher; d) score on question 18 is 6 or higher.\n* Able to use a computer and has internet access.\n* Able to provide informed consent to participate.\n\nExclusion Criteria:\n\n* is below 40 years old.\n* has any comorbid mental disorder or disability that may impede group participation (e.g., personality disorder, learning disability).\n* does not understand English (read, write, listen, and speak).\n* has current active suicidal\u002Fhomicidal ideation.\n* is currently receiving psychological intervention (individual or group).","40 Years",{"count":701,"type":23},30,[26],"The goal of this study is to evaluate the efficacy of group-based ACT intervention in improving the levels of psychological distress in caregivers of stroke survivors. The main questions it aims to answer are:\n\n1. Does group-based ACT intervention improve the levels of psychological distress and QoL in family caregivers of stroke survivors?\n2. Do the levels of psychological flexibility and experiential avoidance in family caregivers of stroke survivors mediate the outcome of the ACT Group?\n\nThe researcher will compare the experimental group (i.e., participants who received group-based ACT intervention) with the control group (i.e., participants who did not receive group-based ACT intervention) to assess whether the group-based ACT intervention is effective in mitigating caregiver stress and improving caregivers' QoL.\n\nParticipants in the experimental group will:\n\n1. Receive a 5-weekly, 1.5-hour group intervention based on the ACT Model;\n2. Complete study measures at pre-treatment, immediate post-treatment, and 2-month follow-up.\n\nParticipants in the control group will not receive the group intervention but will complete the same study measures.",[128,600,30,705,706,707,708,709,29,710,711,712,713,714],"Caregiver Distress","Caregiver Exhaustion","Caregiver Health Related QOL","Caregiver Burden for Those Who Care for Adults With Impaired Functional Status","Caregiver Quality of Life","Caregiver Mental Health","Caregiver Resilience and Stress","Caregiver Sense of Control Over Life","Caregiver Awareness","Caregiver Stress in Chronic Mental Illness","2026-04-29",{"date":717,"type":39},"2026-05-01",{"date":719,"type":39},"2025-09-01",{"date":721,"type":23},"2028-05-31",{"name":723,"class":46},"The Wright Institute"]