Yaşar, Beril NisaTerzioğlu, FüsunNursing2024-07-052024-07-05202202687-46442687-464410.5152/ArcHealthSciRes.2021.210242-s2.0-85125646167https://doi.org/10.5152/ArcHealthSciRes.2021.21024Objective: The aim of this study is to evaluate the care burden and quality of life of caregivers of patients with gynecologic cancer.\rMaterial and Methods: This descriptive study was conducted with 251 individuals who provided care to patients with gynecologic cancer in gynecologic oncology\rservices of a university hospital and a state oncology hospital. The data were collected by a semi-structured questionnaire form, Caregiver Burden Inventory (CBI),\rand Quality of Life Family Version.\rResults: The mean age of the participants was 39.76 ± 14.20; 79.3% of them were female, 65.3% were married, 28.7% were high school graduates, 57.4% were\remployed and 56.2% were unemployed before starting care, 91.2% had health insurance, 58.6% perceived their income as moderate, and 57% had relatives of the\rpatient receiving care. Care burden was statistically significant in terms of gender, marital status, educational level, and degree of affinity with the patient (P < .005).\rThe correlation between caregivers’ quality of life, gender, health insurance, income status, and the degree of affinity with the patient was statistically significant\r(P < .005).\rConclusion: As a result of this study, it was determined that some socio-demographic characteristics of the caregivers of patients with gynecologic cancer affected\rthe care burden and quality of life.eninfo:eu-repo/semantics/openAccessArticleN/AQ4915154