[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100616645":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":10,"centralContacts":10,"locations":10,"responsibleParty":20,"collaborators":10,"id":24,"slug":25,"hasResults":26,"nctId":27,"briefTitle":28,"officialTitle":29,"acronym":10,"eligibilityCriteria":30,"healthyVolunteers":31,"sex":32,"minAge":33,"maxAge":10,"enrollmentInfo":34,"targetDuration":37,"studyType":38,"phases":10,"briefSummary":39,"conditions":40,"keywords":10,"overallStatus":48,"whyStopped":10,"lastUpdateSubmitDate":49,"lastUpdatePostDateStruct":50,"startDateStruct":53,"completionDateStruct":55,"leadSponsor":57,"locationsCount":10},{"fullName":5,"class":6},"Fenerbahce University","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Primary caregivers eighteen and older of hospitalized pediatric cancer patients will be included.",null,"The study includes individuals who provide care for pediatric oncology patients. The research will involve primary caregivers aged 18 years or older who provide care for a child diagnosed with cancer and who are currently hospitalized in the Pediatric Hematology and Oncology Unit of Başakşehir Çam and Sakura City Hospital. The study will examine caregivers' sociodemographic characteristics, quality of life, and caregiving burden levels.",[13],"Behavioral: Assessment of caregiver quality of life and burden",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":10},"BEHAVIORAL","Assessment of caregiver quality of life and burden","This intervention consists of assessing the quality of life and caregiving burden of primary caregivers of children diagnosed with cancer using standardized questionnaires and scales. It does not involve any medical procedures, treatments, or experimental applications. The intervention includes only the administration of data collection tools to caregivers and is therefore distinct from treatment-based interventions used in other clinical studies.",[9],{"type":21,"investigatorFullName":22,"investigatorTitle":23,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"SPONSOR_INVESTIGATOR","Fatma Beyza Akdeniz","Pediatric Nurse","100616645","examination-of-the-relationship-between-quality-of-life-and-caregiving-burden-among-caregivers-of-pediatric-oncology-patients-100616645",false,"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",true,"ALL","18 Years",{"count":35,"type":36},95,"ESTIMATED","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.",[41,42,43,44,45,46,47],"Childhood Cancer","Childhood Cancers","Caregiver Subjective Burden","Primary Caregivers of Children Newly Diagnosed With Cancer","Caregiver","Caregiver Anxiety","Caregiver Health Related QOL","NOT_YET_RECRUITING","2025-12-26",{"date":51,"type":52},"2025-12-31","ACTUAL",{"date":54,"type":36},"2026-01-01",{"date":56,"type":36},"2026-06-30",{"name":22,"class":6}]