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- W4206232214 abstract "Objectives: A pediatric cancer diagnosis can have a significant impact on the quality of life (QOL) of the child. Diagnosis and treatment impact caregiver anxiety/depression symptoms and family functioning, and these in turn may influence child QOL. However, there has been limited longitudinal examination of the impact of both caregiver anxiety/depression symptoms and family functioning on youth QOL at specific points during the early diagnosis and treatment period.Methods: Ninety-six caregivers of youth (diagnosed with leukemia/lymphoma or a solid tumor) reported on their own anxiety/depression symptoms, family functioning, demographic and medical factors, and on their child’s generic and cancer-specific QOL shortly after diagnosis (T1) and 6 months later (T2).Results: Caregiver anxiety/depression symptoms were associated with poorer cancer-specific and generic child QOL within and across time points. Family conflict was associated with youth cancer-related QOL at T1.Conclusions: Attendance to caregiver anxiety/depression symptoms and family functioning, beginning early in the cancer trajectory, is an important aspect of family-centered care. Routine psychosocial screening and triage may help identify and intervene to support both caregiver and child psychosocial well-being." @default.
- W4206232214 created "2022-01-25" @default.
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- W4206232214 date "2022-01-12" @default.
- W4206232214 modified "2023-09-30" @default.
- W4206232214 title "The impact of caregiver anxiety/depression symptoms and family functioning on child quality of life during pediatric cancer treatment: From diagnosis to 6 months" @default.
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- W4206232214 doi "https://doi.org/10.1080/07347332.2021.2015646" @default.
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