4.6 Article

Financial burden for caregivers of adolescents and young adults with cancer

Journal

PSYCHO-ONCOLOGY
Volume 31, Issue 8, Pages 1354-1364

Publisher

WILEY
DOI: 10.1002/pon.5937

Keywords

adolescent; adolescent and young adult oncology; cancer; caregiver; financial burden; financial distress; financial toxicity; oncology; psycho-oncology; young adult

Funding

  1. Wake Forest Baptist Comprehensive Cancer Center's NCI Cancer Center [P30CA012197]
  2. National Cancer Institute (NCI) of the National Institutes of Health [R01CA218398]
  3. Wake Forest Clinical and Translational Science Institute's National Center for Advancing Translational Sciences (NCATS) [ULTR001420]
  4. NCATS [KL2TR001421]

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This study conducted qualitative concept elicitation interviews with caregivers of Adolescent and young adult (AYA) cancer survivors to enhance the existing conceptual model of financial burden. The study identified seven themes related to financial burden, which varied by age group and included areas such as cancer costs, socio-economic impact, strategies to manage costs, and worries about the future. The study also found that COVID-19 has exacerbated financial burden for some caregivers. Developing a reliable self-report measure of financial burden among caregivers of AYA cancer survivors is an important next step.
Objective Adolescent and young adult (AYA) cancer survivors are vulnerable to cancer-related financial burden, which is likely shared by their caregivers. This study aims to enhance an existing conceptual model of financial burden by conducting concept elicitation interviews with caregivers to generate knowledge that can be translated to inform instrumental and psychosocial support in cancer care. Methods Qualitative concept elicitation interviews were conducted with 24 caregivers of AYA cancer survivors (caregivers of adolescents, n = 12; caregivers of emerging adults, n = 12) recruited from four sites. Constant comparative methods were used to identify themes, and results were interpreted and organized into domains of the conceptual model. We also explored COVID-19 related financial impacts among a subset (n = 12) of caregivers. Results Seven themes emerged, which varied by age group and strengthened the conceptualization of the model. Themes centered on: (1) direct and indirect costs of cancer; (2) impact of socioeconomic status on financial burden; (3) caregiver desire to shield AYAs from distress due to financial burden; (4) strategies to manage cancer-related costs; (5) worries about AYAs' financial future; (6) seeking and receiving financial support; and (7) navigating the healthcare system. Findings also revealed that COVID-19 exacerbates financial burden for some caregivers. Conclusions Building upon our prior work, we have adapted the conceptual model of financial burden to reflect perspectives of AYAs, oncology providers, and now, caregivers. An important next step is to develop a reliable and valid self-report measure of financial burden among caregivers of AYA cancer survivors.

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