References
- Adams, K. B., Leibbrandt, S., & Moon, H. (2011). A critical review of the literature on social and leisure activity and wellbeing in later life. Ageing and Society, 31(4), 683–712. doi:https://doi.org/10.1017/S0144686X10001091
- Andreassen, S., Randers, I., Na¨ Slund, E., Stockeld, D., &., & Mattiasson, A. (2007). Informationneeds following a diagnosis of esophageal cancer; self-perceivedinformation needs of patients and family members compared with theperception of health care professional: A pilot study. European Journal of Cancer Care, 16(3), 277–285. doi:https://doi.org/10.1111/j.1365-2354.2006.00742.x
- Axelsson, B., & Sjoden, P. O. (1998). Quality of life of cancer patients and their spouses in palliative home care. Palliative Medicine, 12(1), 29–39. doi:https://doi.org/10.1191/026921698676629560
- Baider, L., & Surbone, A. (2014). Universality of aging: Family caregivers for elderly cancer patients. Frontiers in Psychology, 5(744), 1–7. doi:https://doi.org/10.3389/fpsyg.2014.00744
- Bandura, A. (1997). Self-efficacy. W. H. Freeman and Company.
- Bedim, L. A., Guinan, D. M. (1996). If I could just be selfish …”: Caregivers’ perceptions of their entitlement to leisure. Leisure Sciences, 18(3), 227–240. doi:https://doi.org/10.1080/01490409609513284
- Bedini, L. A. (2002). Family caregivers and leisure: An oxymoron? Parks and Recreation, 37(1), 25–31.
- Bedini, L. A., & Gladwell, N. J. (2006). Barriers to leisure travel of family caregivers: A preliminary examination. Topics in Geriatric Rehabilitation, 22(4), 322–333. doi:https://doi.org/10.1097/00013614-200610000-00007
- Bevans, M., & Sternberg, E. M. (2012). Caregiving burden, stress, and health effects among family caregivers of adult cancer patients. JAMA, 307(4), 398–403. doi:https://doi.org/10.1001/jama.2012.29
- Brinkmann, S. (2011). Towards a theory of rights for qualitative researchers. International Review of Qualitative Research, 4(2), 189–208.
- Burnette, D., Duci, V., & Dhembo, E. (2017). Psychological distress, social support, and quality of life among cancer caregivers in Albania. Psycho-Oncology, 26(6), 779–786. doi:https://doi.org/10.1002/pon.4081
- Cameron, J. I., Franche, R. L., Cheung, A. M., & Stewart, D. E. (2002). Lifestyle interference and emotional distress in family caregivers of advanced cancer patients. Cancer, 94(2), 521–527. doi:https://doi.org/10.1002/cncr.10212
- Carstairs, S. (2000). Quality end-of-life care: The right of every Canadian. https://sencanada.ca/content/sen/committee/362/upda/rep/repfinjun00-e.htm
- Cho, H. (2020). Importance of leisure nostalgia on life satisfaction and leisure participation. The Service Industries Journal, 40(1–2), 90–109. doi:https://doi.org/10.1080/02642069.2019.1567714
- Cho, H., Joo, D., & Chi, C. G. Q. (2019a). Examining nostalgia in sport tourism: The case of US college football fans. Tourism Management Perspectives, 29, 97–104. doi:https://doi.org/10.1016/j.tmp.2018.11.002
- Cho, H., Joo, D., Moore, D., & Norman, W. (2019b). Sport tourists’ nostalgia and its effect on attitude and intentions: A multilevel approach. Tourism Management Perspectives Advance Perspectives, 32, 100563. doi:https://doi.org/10.1016/j.tmp.2019.100563
- Cho, H., Joo, D., & Woosnam, K. (2020). Testing cross-cultural validation of a nostalgia scale for sport tourism: A multilevel analysis. Journal of Hospitality & Tourism Research. Advance Online Publication, doi.org/https://doi.org/10.1177/1096348019899461
- Cho, H., Khoo, E. C., & Lee, H.-W. (2019). Nostalgia, motivation, and intention for international football stadium tourism. Asia Pacific Journal of Tourism Research, 24(9), 912–923. doi:https://doi.org/10.1080/10941665.2019.1653339
- Cho, H., Pyun, D. Y., & Lim, S. H. (2020). Enhancing the stability of the leisure nostalgia scale: Assessment of the measurement invariance between two different leisure populations. Leisure Studies, 39(2), 294–303. doi:https://doi.org/10.1080/02614367.2019.1653356
- Cho, H., Pyun, D. Y., & Wang, C. K. J. (2019). Leisure nostalgia: Scale development and validation. Journal of Leisure Research, 50(4), 330–349. doi:https://doi.org/10.1080/00222216.2019.1602014
- Cho, H., Ramshaw, G., & Norman, W. (2014). A conceptual model for nostalgia in the context of sport tourism: Re-classifying the sporting past. Journal of Sport & Tourism, 19(2), 145–167. doi:https://doi.org/10.1080/14775085.2015.1033444
- Colaizzi, P. F. (1978). Psychological research as the phenomenologist views it. In R. Vaile & M. King (Eds.), Existential phenomenological alternatives for psychology (pp. 48–71). Oxford University Press.
- Coleman, D., & Iso-Ahola, S. E. (1993). Leisure and health: The role of social support and self-determination. Journal of Leisure Research, 25(2), 111–128. doi:https://doi.org/10.1080/00222216.1993.11969913
- Cotrim, H., & Pereira, G. (2008). Impact of colorectal cancer on patient and family: Implications for care. European Journal of Oncology Nursing, 12(3), 217–226. doi:https://doi.org/10.1016/j.ejon.2007.11.005
- Denzin, N. (2003). Performance ethnography: Critical pedagogy and the politics of culture. Thousand Oaks, CA: Sage.
- DesRosier, M. B., Catanzaro, M., & Piller, J. (1992). Living with chronic illness: Social support and the well spouse perspective. Rehabilitation Nursing, 17(2), 87–91. doi:https://doi.org/10.1002/j.2048-7940.1992.tb01519.x
- Dunn, N. J., & Strain, L. A. (2001). Caregivers at risk? Changes in leisure participation. Journal of Leisure Research, 33(1), 32–55. doi:https://doi.org/10.1080/00222216.2001.11949929
- Fletcher, B. S., Miaskowski, C., Given, B., & Schumacher, K. (2012). The cancer family caregiving experience: An updated and expanded conceptual model. European Journal of Oncology Nursing, 16(4), 387–398. doi:https://doi.org/10.1016/j.ejon.2011.09.001
- García‐Villamisar, D. A., & Dattilo, J. (2010). Effects of a leisure programme on quality of life and stress of individuals with ASD. Journal of Intellectual Disability Research, 54(7), 611–619. doi:https://doi.org/10.1111/j.1365-2788.2010.01289.x
- George, L. K. (1983). Caregiver well-being: Correlates and relationships with participation in community self-help groups. Final report to the Andrus Foundation. Center for the Study of Aging, Duke University.
- Gill, P., Stewart, K., Treasure, E., & Chadwick, B. (2008). Methods of data collection in qualitative research: Interviews and focus groups. British Dental Journal, 204(6), 291–295. doi:https://doi.org/10.1038/bdj.2008.192
- Gilligan, C. (1982). In a different voice. Cambridge, MA: Harvard University Press.
- Given, B. A., Given, C. W., & Kozachik, S. (2001). Family support in advanced cancer. CA: A Cancer Journal for Clinicians, 51(4), 213–231. doi:https://doi.org/10.3322/canjclin.51.4.213
- Grant, J. S., Glandon, G. L., Elliott, T. R., Giger, J. N., & Weaver, M. (2004). Caregiving problems and feelings experienced by family caregivers of stroke survivors the first month after discharge. International Journal of Rehabilitation Research, 27(2), 105–111. doi:https://doi.org/10.1097/01.mrr.0000127639.47494.e3
- Greenson, R. R. (1953). On boredom. Journal of the American Psychoanalytic Association, 1(1), 7–21. doi:https://doi.org/10.1177/000306515300100102
- Grunfeld, E., Coyle, D., Whelan, T., Clinch, J., Reyno, L., Earle, C. C., Willan, A., Viola, R., Coristine, M., Janz, T. & Glossop, R. (2004). Family caregiver burden: Results of a longitudinal study of breast cancer patients and their principal caregivers. Canadian Medical Association Journal, 170(12), 1795–1801. doi:https://doi.org/10.1503/cmaj.1031205
- Hopkinson, J., & Corner, J. (2006). Helping patients with advanced cancer live with concerns about eating: A challenge for palliative care professionals. Journal of Pain and Symptom Management, 31(4), 293–305. doi:https://doi.org/10.1016/j.jpainsymman.2005.09.005
- Iso-Ahola, S. E., & Park, C. J. (1996). Leisure-related social support and self-determination as buffers of stress-illness relationship. Journal of Leisure Research, 28(3), 169–187. doi:https://doi.org/10.1080/00222216.1996.11949769
- Iwasaki, Y. (2003). Examining rival models of leisure coping mechanisms. Leisure Sciences, 25(2-3), 183–206. doi:https://doi.org/10.1080/01490400306560
- Jensen, S., & Given, B. (1993). Fatigue affecting family caregivers of cancer patients. Supportive Care in Cancer, 1(6), 321–325. doi:https://doi.org/10.1007/BF00364970
- Kelly, J. R. (1996). Leisure (3rd ed.). Prentice Hall.
- Kershaw, T., Northouse, L. L., Kritpracha, C., Schafenacker, A., & Mood, D. (2004). Coping strategies and quality of life in women with advanced breast cancer and their family caregivers. Psychology & Health, 19(2), 139–155. doi:https://doi.org/10.1080/08870440310001652687
- King, N. J., Tonge, B. J., Mullen, P., Myerson, N., Heyne, D., Rollings, S., Martin, R., & Ollendick, T. H. (2000). Treating sexually abused children with posttraumatic stress symptoms: A randomized clinical trial. Journal of the American Academy of Child & Adolescent Psychiatry, 39(11), 1347–1355. doi:https://doi.org/10.1097/00004583-200011000-00008
- Kitrungrote, L., & Cohen, M. Z. (2006). Quality of life of family caregivers of patients with cancer. Oncology Nursing Forum, 33(3), 625–632. doi:https://doi.org/10.1188/06.ONF.625-632
- Klapp, O. E. (1986). Overload and boredom: Essays on the quality of life in the information society. Greenwood Publishing Group Inc.
- Lazarus, R. S., & Folkman, S. (1984). Stress, appraisal, and coping. Springer Publishing Company.
- Lincoln, Y. S., & Guba, E. G. (1985). Naturalistic inquiry. Sage.
- Losada, A., Pérez-Peñaranda, A., Rodriguez-Sanchez, E., Gomez-Marcos, M. A., Ballesteros-Rios, C., Ramos-Carrera, I. R., Campo-de la Torre, M. Á., & García-Ortiz, L. (2010). Leisure and distress in caregivers for elderly patients. Archives of Gerontology and Geriatrics, 50(3), 347–350. doi:https://doi.org/10.1016/j.archger.2009.06.001
- Lynch, S. H., & Lobo, M. L. (2012). Compassion fatigue in family caregivers: A Wilsonian concept analysis. Journal of Advanced Nursing, 68(9), 2125–2134. doi:https://doi.org/10.1111/j.1365-2648.2012.05985.x
- Marks, N., Lambert, J. D., & Choi, H. (2002). Transitions to caregiving, gender, and psychological wellbeing: A prospective U.S. national study. Journal of Marriage and Family, 64(3), 657–667. doi:https://doi.org/10.1111/j.1741-3737.2002.00657.x
- Markula, P., & Silk, M. L. (2011). Qualitative research for physical culture. London: Palgrave Macmillan.
- Mundy, J. (1998). Leisure education: Theory and practice (2nd ed.). Sagamore.
- National Cancer Center. (2019, January). National cancer center newsletter: 1.73 milion cancer patients cancer survival rate increases. Breast cancer increases for 17 years. http://ncc.re.kr/webzine/201901/sub_05.jsp
- Neulinger, J. (1974). The psychology of leisure. Charles C Thomas.
- Pearlin, L., I., Mullan, J. T., Semple, S. J., & Skaff, M. M. (1990). Caregiving and the stress process: An overview of concepts and their measures. The Gerontologist, 30(5), 583–594. doi:https://doi.org/10.1093/geront/30.5.583
- Porter, E. J. (2000). Setting aside the identity furor: Staying her story-course of sameness. Qualitative Inquiry, 6(2), 238–250. doi:https://doi.org/10.1177/107780040000600205
- Reinhard, S. C., Feinberg, L. F., Choula, r., & Houser, A. (2015). Valuing the invaluable: 2015 update. Washington, DC: AARP Public Policy Institute.
- Rose, L., Mallinson, R. K., & Walton-Moss, B. (2002). A grounded theory of families responding to mental illness. Western Journal of Nursing Research, 24(5), 516–536. doi:https://doi.org/10.1177/019394502400446397
- Ruskin, H., & Sivan, A., Eds. (1995). Leisure education toward the 21st century. Brigham Young University.
- Sadala, M. L. A., Stolf, N. G., Bocchi, E. A., & Bicudo, M. A. V. (2013). Caring for heart transplant recipients: The lived experience of primary caregivers. Heart & Lung, 42(2), 120–125. doi:https://doi.org/10.1016/j.hrtlng.2012.09.006
- Scheier, M. F., Carver, C. S., & Bridges, M. W. (2001). Optimism, pessimism, and psychological well-being. Optimism and Pessimism: Implications for Theory. Research, and Practice, 1, 189–216.
- Schulz, R., Hebert, R. S., Dew, M. A., Brown, S. L., Scheier, M. F., Beach, S. R., Czaja, S. J., Martire, L. M., Coon, D., Langa, K. M., Gitlin, L. N., Stevens, A. B., & Nichols, L. (2007). Patient suffering and caregiver compassion: New opportunities for research, practice, and policy. The Gerontologist, 47(1), 4–13. doi:https://doi.org/10.1093/geront/47.1.4
- Shields, C. G. (1992). Family interaction and caregivers of Alzheimer’s disease patients: Correlates of depression. Family Process, 31(1), 19–33. doi:https://doi.org/10.1111/j.1545-5300.1992.00019.x
- Smith, B., & Sparkes, A. C. (2009). Narrative analysis and sport and exercise psychology: Understanding lives in diverse ways. Psychology of Sport and Exercise, 10(2), 279–288. doi:https://doi.org/10.1016/j.psychsport.2008.07.012
- Sörensen, S., & Pinquart, M. (2005). Racial and ethnic differences in the relationship of caregiving stressors, resources, and sociodemographic variables to caregiver depression and perceived physical health. Aging & Mental Health, 9(5), 482–495. doi:https://doi.org/10.1080/13607860500142796
- Spillers, R. L., Wellisch, D. K., Kim, Y., Matthews, A., & Baker, F. (2008). Family caregivers and guilt in the context of cancer care. Psychosomatics, 49(6), 511–519. doi:https://doi.org/10.1176/appi.psy.49.6.511
- Stajduhar, K. I., Martin, W., & Cairns, M. (2010). What makes grief difficult? Perspectives from bereaved family caregivers and healthcare providers of advanced cancer patients. Palliative and Supportive Care, 8(3), 277–289. doi:https://doi.org/10.1017/S1478951510000076
- Stumbo, N. J., & Peterson, C. A. (2009). Therapeutic recreation program design: Principles and procedures (5th ed.). Pearson.
- Teitelman, J., & Watts, J. H. (2004). Family members’ recommendations for achieving a mental break from caring for a loved one with Alzheimer’s disease. Alzheimer’s Care Today, 5(3), 252–260.
- van Ryn, M., Sanders, S., Kahn, K., van Houtven, C., Griffin, J. M., Martin, M., Atienza, A. A., Phelan, S., Finstad, D., & Rowland, J. (2011). Objective burden, resources, and other stressors among informal cancer caregivers: A hidden quality issue? Psycho-Oncology, 20(1), 44–52. doi:https://doi.org/10.1002/pon.1703
- Waldrop, D. P., Meeker, M. A., Kerr, C., Skretny, J., Tangeman, J., & Milch, R. (2012). The nature and timing of family-provider communication in late-stage cancer: A qualitative study of caregivers’ experiences. Journal of Pain and Symptom Management, 43(2), 182–194. doi:https://doi.org/10.1016/j.jpainsymman.2011.04.017
- 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. doi:https://doi.org/10.1016/S0889-8588(05)70288-4
- Yun, Y. H., Rhee, Y. S., Nam, S. Y., Park, S. M., Lee, J. S., Park, M. H., Choe, W. S., Lee, C. G. & Won, J. H. (2005). The socioeconomic impact of terminal cancer on patients´ families and its associated factors. The Korean Academy of Family Medicine, 26(1), 31–39.
- Zhang, A. Y., & Siminoff, L. A. (2003). The role of the family in treatment decision making by patients with cancer. Oncology Nursing Forum, 30(6), 1022–1028. doi:https://doi.org/10.1188/03.ONF.1022-1028