[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"caregiver-health-related-qol\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:caregiver-health-related-qol":32},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,54],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":42,"lastUpdatePostDateStruct":43,"startDateStruct":46,"completionDateStruct":48,"leadSponsor":50,"locationsCount":53},"100633559","act-group-for-family-caregivers-of-stroke-survivors-100633559",false,"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).",true,"ALL","40 Years",{"count":20,"type":21},30,"ESTIMATED","INTERVENTIONAL",[24],"NA","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.",[27,28,29,30,31,32,33,34,35,36,37,38,39,40],"Caregiver Stress","Caregiver Stress Syndrome","Caregiver Burnout","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 Burden","Caregiver Mental Health","Caregiver Resilience and Stress","Caregiver Sense of Control Over Life","Caregiver Awareness","Caregiver Stress in Chronic Mental Illness","RECRUITING","2026-04-29",{"date":44,"type":45},"2026-05-01","ACTUAL",{"date":47,"type":45},"2025-09-01",{"date":49,"type":21},"2028-05-31",{"name":51,"class":52},"The Wright Institute","OTHER",1,{"id":55,"slug":56,"hasResults":11,"nctId":57,"briefTitle":58,"officialTitle":59,"acronym":4,"eligibilityCriteria":60,"healthyVolunteers":16,"sex":17,"minAge":61,"maxAge":4,"enrollmentInfo":62,"targetDuration":64,"studyType":65,"phases":4,"briefSummary":66,"conditions":67,"keywords":4,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":4},"100616645","examination-of-the-relationship-between-quality-of-life-and-caregiving-burden-among-caregivers-of-pediatric-oncology-patients-100616645","NCT07308301","Examination of the Relationship Between Quality of Life and Caregiving Burden Among Caregivers of Pediatric Oncology Patients","EXAMİNATİON OF THE RELATİONSHİP BETWEEN QUALİTY OF LİFE AND CAREGİVİNG BURDEN AMONG CAREGİVERS OF PEDİATRİC OCOLOGY PATİENTS","Inclusion Criteria:\n\n* Being a family member who provides care for a child aged 0-18 years diagnosed with cancer\n* The child being in the active treatment phase (chemotherapy, radiotherapy, post-surgical follow-up, etc.)\n* Being able to read and write in Turkish and having sufficient literacy to complete the research questionnaire\n* Willingness to participate in the study\n\nExclusion Criteria:\n\n* Not being the primary caregiver of the child (serving only as a short-term companion)\n* Being unable to complete the questionnaire due to a psychiatric diagnosis or communication difficulties\n* The child having a disability","18 Years",{"count":63,"type":21},95,"4 Months","OBSERVATIONAL","Primary Aim\n\nThe primary aim of this study is to determine the quality of life and caregiving burden levels of caregivers of pediatric oncology patients and to examine the relationship between these two variables.\n\nSecondary Aims\n\nTo evaluate the differences between caregivers' sociodemographic characteristics (age, gender, education level, marital status, income level, etc.) and their quality of life.\n\nTo examine the differences between caregivers' sociodemographic characteristics and their caregiving burden levels.\n\nTo determine whether caregivers' quality of life and caregiving burden differ according to the diagnosis and treatment characteristics of pediatric oncology patients (duration of diagnosis, type of treatment, frequency of hospitalization, etc.).\n\nSignificance of the Study\n\nChildhood cancer is a process that deeply affects not only the patient but also the family, particularly the caregivers. Family members who provide care for children often face intense physical, psychological, social, and economic burdens. These challenges reduce caregivers' quality of life and increase their caregiving burden.\n\nIdentifying the relationship between the quality of life and caregiving burden among caregivers of pediatric oncology patients is highly important in planning support services for families during the care process and in strengthening family-centered care practices by healthcare professionals.\n\nThe findings of this study will contribute to the development of family-centered approaches in nursing care, the design of psychosocial support programs, and a better understanding of caregivers' needs.",[68,69,70,71,72,73,32],"Childhood Cancer","Childhood Cancers","Caregiver Subjective Burden","Primary Caregivers of Children Newly Diagnosed With Cancer","Caregiver","Caregiver Anxiety","NOT_YET_RECRUITING","2025-12-26",{"date":77,"type":45},"2025-12-31",{"date":79,"type":21},"2026-01-01",{"date":81,"type":21},"2026-06-30",{"name":83,"class":52},"Fatma Beyza Akdeniz"]