行政院衛生署(2008)。衛生資訊—衛生統計—死因統計。台北:行政院衛生署。
余德慧、石世明、夏淑怡、王英偉(2006)。病床陪伴的心理機制:一個二元複合模式的提出。應用心理研究，29，71-100。
林耀盛(2006)。聆聽受苦之聲:從「咱們」關係析究慢性病照顧。應用心理研究，29，183-212。
胡至家(2005)。憂鬱傾性、親密關係與乳癌術後婦女身體意象關係之探討。高雄醫學大學行為科學研究所，碩士論文，未出版，高雄。
姚開屏(2002 a)。台灣版世界衛生組織生活品質問卷之發展與應用。臺灣醫學，6(3)，193-200。
姚開屏(2002 b)。健康相關生活品質概念與測量原理之簡介。臺灣醫學，6(2)，183-192。
姚開屏(2005)。台灣簡明版世界衛生組織生活品質問卷之發展及使用手冊。台北:台灣版世界衛生組織生活品質問卷發展小組。
侯懿真(2006)。悲悼的歧異:癌症新近喪偶者傷逝療癒歷程的建構詮釋。高雄醫學大學行為科學研究所碩士論文，未出版，高雄。
陳怡靜(2001)。婦癌患者身體心像、社會支持和憂鬱的對照研究。高雄醫學大學護理研究所碩士論文，未出版，高雄。 陳麗如(2004)。居家照護病患主要照顧者人格韌性健康狀況與生活品質相關性探討。高雄醫學大學護理研究所碩士論文，未出版，高雄。
湯梅芬(2004)。居家運動訓練指導改善癌症病患睡眠障礙與生活品質成效之探討。台北醫學大學護理學研究所碩士論文，未出版，高雄。
蔡盈盈(2006)。乳癌患者家屬照顧者的因應，社會支持與生活品質之相關性初探。國立成功大學行為醫學研究所碩士論文，未出版，台南。
Banthia, R., Malcarne, V. L., Varni, J. W., Ko, C. M., Sadler, G. R., & Greenbergs, H. L.(2003). The effects of dyadic strength and coping styles on psychological distress in couples faced with prostate cancer. Journal of Behavioral Medicine, 26, 31-52.
Barrera, M., Sandler, I., & Ramsay, T. (1981). Preliminary development of a scale of social support: Studies on college students. American Journal of Community Psychology, 9, 435-447.
Baumgarten, M., Battista, R. N., Infante-Rivard, C., Finley, J. A., Becker, R., & Gauthier, S. (1992). The psychological and physical health of family members caring for an elderly person with dementia. Journal of Clinical Epidemiology, 45(1), 61-70.
Ben-Zur, G., Gilbar, O., & Lev, S. (2001). Coping with breast cancer: Patient, spouse, and dyad models. Psychosomatic Medicine, 63(1), 32-39.
Berg-Weger, M., Rubio, D. M., & Tebb, S. S. (2000). Depression as a mediator: Viewing caregiver well-being and strain in a different light. Families in Society: The Journal of Contemporary Human Services, 81(2), 162-173.
Bleiker, E. M., Pouwer, F., van der Ploeg, H. M., Leer, J. W., & Ader, H. J. (2000). Psychological distress two years after diagnosis of breast cancer: Frequency and prediction. Patient Education and Counseling, 40(3), 209-217.
Cheng, C. (1998). Getting the right kind of support: Functional differences in the types of social support on depression for Chinese adolescents. Journal of Clinical Psychology, 54(6), 845-849.
Cheung, J., & Hocking, P. (2004). Caring as worrying: The experience of spousal carers. Journal of Advanced Nursing, 47, 475-482.
Chien, C. P., & Cheng, T. A. (1985). Depression in Taiwan: Epidemiological survey utilizing CES-D. Seishin Shinkeigaku Zasshi (Psychiatria et Neurologia Japonica), 87(5), 335-338.
Cohen, D., Luchins, D., Eisdorfer, C., Paveza, G., Ashford, J. W., & Gorelick, P. (1990). Caring for relatives with Alzheimer’s disease: The mental health risks to spouses, adult children and other family caregivers. Behavior, Health and Aging, 1(3), 171-182.
Cull, A., Stewart, M., & Altman, D. C. (1995). Assessment of and intervention for psycho- social problems in routine oncology practice. British Journal of Cancer, 72, 229-235.
Dakof, G. A., & Taylor, S. E. (1990). Victims' perceptions of social support: What is help- ful from whom? Journal of Personality and Social Psychology, 58(1), 80-89.
Downe-Wamboldt, B., Butler, L., & Coulter, L.(2006). The relationship between meaning of illness, social support, coping strategies, and quality of life for lung cancer patients and their family members. Cancer Nursing, 29(2), 111-119.
Feldman, B. N., & Broussard, C. A. (2006). Men’s adjustment to their partners’ breast cancer: A dyadic coping perspective. Health Social Work, 31, 117-127.
Hagedoorn, M., Sanderman, R., Buunk, B. P., & Wobbes, T. (2002). Failing in spousal caregiving: The 'identity-relevant stress' hypothesis to explain sex differences in care- giver distress. British Journal of Health Psychology, 7(4), 481-494.
Hipkins, J., Whitworth, M., Tarrier, N., & Jayson, G. (2004). Social support, anxiety and depression after chemotherapy for ovarian cancer: A prospective study. British Jour- nal of Health Psychology, 9, 569-581.

Hodges, L. J., Humphris, G. M., & Macfarlane, G. (2005). A meta-analytic nvestigation of the relationship between the psychological distress of cancer patients and their carers.Social Science and Medicine, 60(1), 1-12.
Hurt, G. J., McQuellon, R. P., & Barrett, R. J. (1994). After treatment ends: Neutral time.Cancer Practice, 2, 417-421.
Kalnins, I. (2006). Caring for the terminally ill: Experiences of Latvian family caregiver.International Nursing Review, 53, 129-135.
Lim, J-W., & Zebrack, B. (2004). Caring for family members with chronic physical illness: A critical review of caregiver literature. Health and Quality of Life Outcome, 2(50). Retrieved June 25, 2006 from http://www.hqlo.com/content /2/1/50
Little, M., & Sayers, E. J. (2004). While there’s life...Hope and the experience of cancer. Social Science and Medicine, 59, 1329-1337.
Manne, S., Taylor, K., Dougherty, J., & Kemeny, N. (1997). Supportive and negative responses in the partner relationship: Their association with psychological adjustment among individuals with cancer. Journal of Behavioral Medicine, 20(2), 101-125.
Martire, L. M., Stephens, M. A., Druley, J. A., & Wojno, W. C. (2002). Negative reactions to received spousal care: Predictors and consequences of miscarried support. Health Psychology, 21(2), 167-176.
Meshefedjian, G., McCusker, J., Bellavance, F., & Baumgarten, M. (1998). Factors associated with symptoms of depression among informal caregivers of demented elders in the community. Gerontologist, 38(2), 247-253.
Middelboe, T., Ovesen, L., Mortensen, E. L., & Bech, P. (1994). Depressive symptoms in cancer patients undergoing chemotherapy: A psychometric analysis. Psychotherapy and Psychosomatics, 61(3-4), 171-177.
Milne, D. J., Mulder L. L., Beelen H. C. M., Schofield, P., Kempen, G. I. J. M., & Aranda, S. (2006). Patients’ self-report and family caregivers’ perception of quality of life in patients with advanced cancer: How do they compare? European Journal of Cancer Care, 15, 125-132.
Newby, N. M. (1996). Chronic illness and the family life-cycle. Journal of Advanced Nursing, 23(4), 786-791.
Newport, D. J., & Nemeroff, C. B. (1998). Assessment and treatment of depression in the cancer patient. Journal of Psychosomatic Research, 45, 215-237.
Newsom, J. T. (1999). Another side to caregiving: Negative reactions to being helped.Current Directions in Psychological Science, 8(6), 183-187.
Noonan, A. E., & Tennstedt, S. L. (1997). Meaning in caregiving and its contribution to caregiver well-being. Gerontologist, 37(6), 785-794
Norton, T. R., Manne, S. L., Rubin, S., Hernandez, E., & Carlson, J. (2005). Ovarian cancer patients’ psychological distress: The role of physical impairment, perceived unsupportive family and friend behaviors, perceived control, and self-esteem. Health Psychology, 24, 143-152.
O’Connor, D. W., Pollitt, P. A., Roth, M., Brook, C. P. B., & Reiss, B. B. (1990). Memory complaints and impairment in normal, depressed and demented elderly persons iden- tified in a community survey. Archives of General Psychiatry, 47, 224-227.
O’Reilly, D., Connolly, S., Rosato, M., & Patterson, C. (2008). Is caring associated with an increased risk of mortality? A longitudinal study. Social Science & Medicine, 67, 1282-1290.
Pearman, T. (2003). Quality of life and psychosocial adjustment in gynecologic cancer survivors. Health and Quality of Life Outcomes, 1(33). Retrieved Novenber 19, 2006 from http://www.hqlo.com/content/1/1/33
Pitts, M., & Phillips, K. (2000). The psychology of health: An introduction (2nd ed.). Lon- don, UK: Routledge.
Reynolds, J. S., & Perrin, N. A. (2004). Mismatches in social support and psychosocial adjustment to breast cancer. Health Psychology, 23(4), 425-430.
Sarafino, E. P. (2008). Health psychology: Biopsychosocial interactions (6th ed.). New York, NY: John Wiley & Sons.
Sellick, S. M., & Crooks, D. L. (1999). Depression and cancer: An appraisal of the literature for prevalence, detection and practice guideline development for psychological interventions. Psycho-Oncology, 8, 315-333.
Silverstein, M., Chen, X., & Heller, K. (1996). Tou much of a good thing? Intergenerational soaul support and pecchologial well-being of older parents. Journal of Marni- age and Family, 58, 970-982.
Smerglia, V. L., & Deimling, G. T. (1997). Care-related decision-making satisfaction and caregiver well-being in families caring for older members. The Gerontologist, 37(5), 658-665.
Soothill, K., Morris, S. M., Harman, J. C., Thomas, C., Francis, B., & MCIllmurray, M. B. (2002). Cancer and faith. Having faith- does it make a difference among patients and their informal carers? Scandinavian Journal of Caring Sciences, 16(3), 256-263.
Van Manen, M.(1998). Modalities of body experience in illness and health. Qualitative Health Research, 8(1), 7-24.
Wenzel, L., DeAlba, I., Habbal, R., Kluhsman, B. C., Fairclough, D., & Krebs, L. U. (2005). Quality of life in long-term cervical cancer survivors. The Women’s Oncology Review, 5, 157-158.
Winkeler, M., Filipp, S.-H., & Aymanns, P. (2006). Direct and indirect strategies of mobilization as determinants of social support provided for cancer patients. Journal of Applied Psychology, 36, 248-267.
Yao, G., Chung, C. W., Yu, C. F., & Wang, J. D. (2002). Development and verification of validity and reliability of the WHOQOL-BRIEF Taiwan version. Journal of Formosan Medical Assosiation, 101(5), 342-351.