REFERENCES
- Ayamann, P., Filipp, S.H., & Klauer, T. (1995). Family support and coping with cancer: Some determinants and adaptive correlates. British Journal of Social Psychology, 34, 107–124.
- Belasco, A.G., & Sesso, R. (2002). Burden and quality of life of caregivers for hemodialysis patients. American Journal of Kidney Diseases, 39(4), 805–812.
- Brinkley, D. (1983). Emotional distress during cancer chemotherapy. British Medical Journal, 286, 663–664.
- Cassileth, B.R., Lusk, E.J., Strouse, T.B., Miller, D.S., Brown, L.L., & Cross, P.A. (1985). A psychological analysis of cancer patients and their next-of-kin. Cancer, 55(1), 72–76.
- Celik, G., Annagur, B.B., Yılmaz, M., Demir, T., & Kara, F. (2012). Are sleep and life quality of family caregivers affected as much as those of hemodialysis patients. General Hospital Psychiatry, 34(5), 518–524.
- Cohen, S., & Wills, T.A. (1985). Stress, social support and buffering hypothesis. Psychological Bulletin, 98(2), 310–357.
- Daneker, B., Kimmel, P.L., Ranich, T., & Peterson, R.A. (2001). Depression and marital dissatisfaction in patients with end-stage renal disease and in their spouses. American Journal of Kidney Diseases, 38(4), 839–846.
- Dunkel-Schetter, C. (1984). Social support and cancer: Findings based on patient interviews and their implications. Journal of Social Issues, 40(4), 77–98.
- Gao, X., Prigerson, H.G., Diamond, E.L., Zhang, B., Wright, A.A., Meyer, F., &Maciejewski, P.K. (2013). Minor cognitive impairments in cancer patients magnify the effect of caregiver preferences on end-of-life care. Journal of Pain and Symptom Management, 45(4), 650–659.
- Given, B.A., Given C.W., & Kozachik S. (2001). Family support in advanced cancer. CA: A Cancer Journal for Clinicians, 51(4), 213–231.
- Harding, R., & Higginson, I.J. (2003). What is the best way to help caregivers in cancer and palliative care? A systematic literature review of interventions and their effectiveness. Palliative Medicine, 17(1), 63–74.
- King, R.M. (1998). Support for patients receiving dialysis and their caregivers. American Nephrology Nurses’ Association Journal, 25(4), 431–432.
- Lichtman, R.R., Taylor, S.E., & Wood, J.V. (1987). Social support and marital adjustment after breast cancer. Journal of Psychosocial Oncology, 5(3), 47–74.
- Ockerby, C., Livingston, P., O’Connell, B., & Gaskin, C.J. (2013). The role of informal caregivers during cancer patients’ recovery from chemotherapy. Scandinavian Journal of Caring Sciences, 27(1), 147–55.
- Pasacrets, J.V., & McCorkle, R. (2000). Cancer care: Impact of interventions on caregiver outcomes. Annual Review of Nursing Research, 18, 127–134.
- Reis, J, McGinty, B, & Jones, S (2003). An e-learning caregiving program for prostate cancer patients and family members. Journal of Medical Systems, 27(1), 1–12.
- Shelby, R.A., Taylor, K.I., Kerner, L.F., Coleman, E., & Blum, D. (2002). The role of community-based and philanthropic organizations in meeting cancer patients and caregiver needs. CA: A Cancer Journal for Clinicians, 52(4), 229–246.
- Tang, S.T., Chang, W.C., Chen, J.S., Wang, H.M., Shen, W.C., Li, C.Y., & Liao, Y.C. (2012). Course and predictors of depressive symptoms among family caregivers of terminally ill cancer patients until their death. Psychooncology, 22(6), 1312–1318.
- Vahon, M.L. (1998). Caring for the caregiver in oncology and palliative care. Seminars in Oncology Nursing, 14(2), 152–157.
- Weitzner, M.A., Haley, W.E., & Chen, H. (2000). The family caregiver of the older cancer patient. Hematology/Oncology Clinics of North America, 14(1), 269–281.
- Wortman, C.B., & Dunkel-Schetter, C. (1979). Interpersonal relationship and cancer: A theoretical analysis. Journal of Social Issues, 351, 120–155.
- Zhang, B., Nilsson, M.E., & Prigerson, H.G. (2012). Factors important to patients’ quality of life at the end of life. Archives of Internal Medicine, 172(15), 1133–1142.