Besser, L. M., & Galvin, J. E. (2018). Perceived burden among caregivers of patients with frontotemporal degeneration in the United States. International psychogeriatrics, 1-11. doi: https://doi.org/10.1017/S104161021800159X
Boots, L. M., de Vugt, M. E., Kempen, G. I., & Verhey, F. R. (2016). Effectiveness of the blended care self-management program “Partner in Balance” for early-stage dementia caregivers: study protocol for a randomized controlled trial. Trials, 17(1), 231. doi: https://doi.org/10.1186/s13063-016-1351-z
Cheng, S. T. (2017). Dementia caregiver burden: A research update and critical analysis. Current psychiatry reports, 19(9), 64. doi: https://doi.org/10.1007/s11920-017-0818-2
Cheung, D. S. K., Ho, K. H. M., Cheung, T. F., Lam, S. C., & Tse, M. M. Y. (2018). Anticipatory grief of spousal and adult children caregivers of people with dementia. BMC palliative care, 17(1), 124. doi: https://doi.org/10.1186/s12904-018-0376-3
Chiao, C. Y., Wu, H. S., & Hsiao, C. Y. (2015). Caregiver burden for informal caregivers of patients with dementia: a systematic review. International nursing review, 62(3), 340-350. doi: https://doi.org/10.1111/inr.12194
de Labra, C., Millán-Calenti, J. C., Buján, A., Núñez-Naveira, L., Jensen, A. M., Peersen, M.C.,…Maseda, A. (2015). Predictors of caregiving satisfaction in informal caregivers of people with dementia. Archives of gerontology and geriatrics, 60, 380-388. doi:10.1016/j.archger.2015.03.002
Donath, C., Luttenberger, K., Graessel, E., Scheel, J., Pendergrass, A., & Behrndt, E. M. (2019). Can brief telephone interventions reduce caregiver burden and depression in caregivers of people with cognitive impairment?-long-term results of the German day-care study (RCT). BMC geriatrics, 19(1), 196. doi: https://doi.org/10.1186/s12877-019-1207-y
Fields, N. L., Xu, L., & Miller, V. J. (2019). Caregiver burden and desire for institutional placement—The roles of positive aspects of caregiving and religious coping. American journal of Alzheimer's disease & other dementias ®, 34(3), 199-207. doi: https://doi.org/10.1177/1533317519826217
Fountoulakis, K. N., Tsolaki, M., Iacovides, A., Yesavage, J., O’hara, R., Kazis, A., & Ierodiakonou, C. (1999). The validation of the short form of the Geriatric Depression Scale (GDS) in Greece. Aging clinical and experimental research, 11(6), 367-372. doi: https://doi.org/10.1007/BF03339814
Fukawa, T. (2018). Prevalence of dementia among the elderly population in Japan. Health and primary care, 2(4),1-6. doi: https://doi.org/10.1007/BF03339814
George, D., & Mallery, M. (2003). Using SPSS for Windows step by step: a simple guide and reference. 4th ed. Boston, MA: Allyn & Bacon.
Gorsuch, R. L. (1983). Factor analysis Lawrence Erlbaum Associates. Hillsdale, NJ.
Harris, G. M., Durkin, D. W., Allen, R. S., DeCoster, J., & Burgio, L. D. (2011). Exemplary care as a mediator of the effects of caregiver subjective appraisal and emotional outcomes. The gerontologist, 51(3), 332-342. doi: https://doi.org/10.1093/geront/gnr003
Hilgeman, M. M., Allen, R. S., DeCoster, J., & Burgio, L. D. (2007). Positive aspects of caregiving as a moderator of treatment outcome over 12 months. Psychology and aging, 22(2), 361. doi: https://doi.org/10.1037/0882-7974.22.2.361
Herrmann, N., Mittmann, N., Silver, I. L., Shulman, K. I., Busto, U. A., Shear, N. H., & Naranjo, C. A. (1996). A validation study of the Geriatric Depression Scale short form. International journal of geriatric psychiatry, 11(5), 457-460. doi: https://doi.org/10.1002/(SICI)1099-1166(199605)11:5<457::AID-GPS325>3.0.C O;2-2
Jütten, L. H., Mark, R. E., & Sitskoorn, M. M. (2019). Empathy in informal dementia caregivers and its relationship with depression, anxiety, and burden. International journal of clinical and health psychology , 19(1), 12-21. doi: https://doi.org/10.1016/j.ijchp.2018.07.004
Kajiwara, K., Nakatani, H., Ono, M., & Miyakoshi, Y. (2015). Positive appraisal of in ‐ home family caregivers of dementia patients as an influence on the continuation of caregiving. Psychogeriatrics, 15(1), 26-31. doi: https://doi.org/10.1111/psyg.12074
Kasahara, H., Kada H., and Yanagawa, Y. (1995). Rounen seisin igaku kanren ryouiki de mochiirareru sokudo; Utsu joutai wo hyukasurutameno sokudo (1), Rounenseisinnigakuzasshi, 6(6), 757-766. in Japanese.
Kinney, J. M., & Stephens, M. A. P. (1989). Hassles and uplifts of giving care to a family member with dementia. Psychology and aging, 4(4), 402. doi: https://doi.org/10.1037/0882-7974.4.4.402
Las Hayas, C., López de Arroyabe, E., & Calvete, E. (2014). Positive aspects of caregiving in Spanish caregivers of individuals with acquired brain injury. Rehabilitation psychology, 59(2), 193. doi: https://doi.org/10.1037/a0035622 Lawton,
M. P., Kleban, M. H., Moss, M., Rovine, M., & Glicksman, A. (1989). Measuring caregiving appraisal. Journal of gerontology, 44(3), P61-P71. doi: https://doi.org/10.1093/geronj/44.3.P61
Lesher, E. L., & Berryhill, J. S. (1994). Validation of the geriatric depression scale – short form among inpatients. Journal of clinical psychology, 50(2), 256-260. doi: https://doi.org/10.1002/1097-4679(199403)50:2<256::AID-JCLP2270500218>3. 0.CO;2-E
Liew, T. M., Tai, B. C., Yap, P., & Koh, G. C. H. (2019). Comparing the effects of grief and burden on caregiver depression in dementia caregiving: a longitudinal path analysis over 2.5 years. Journal of the American medical directors association, 20(8), 977-983. doi: https://doi.org/10.1016/j.jamda.2018.11.016
Liu, S., Li, C., Shi, Z., Wang, X., Zhou, Y., Liu, S., ... & Ji, Y. (2017). Caregiver burden and prevalence of depression, anxiety and sleep disturbances in Alzheimer's disease caregivers in China. Journal of clinical nursing, 26(9-10), 1291-1300. doi: https://doi.org/10.1111/jocn.13601
Lloyd, J., Patterson, T., & Muers, J. (2016). The positive aspects of caregiving in dementia: A critical review of the qualitative literature. Dementia, 15(6), 1534-1561. doi: https://doi.org/10.1177/1471301214564792
Lou, V. W., Lau, B. H. P., & Cheung, K. S. L. (2015). Positive aspects of caregiving (PAC): Scale validation among Chinese dementia caregivers (CG). Archives of gerontology and geriatrics, 60(2), 299-306. doi: https://doi.org/10.1016/j.archger.2014.10.019
Lyons, J. S., Strain, J. J., Hammer, J. S., Ackerman, A. D. & Fulop, G. (1990) Reliability, validity and temporal stability of the Geriatric Depression Scale in hospitalized elderly. The international journal of psychiatry in medicine , 19, 203-209. doi: https://doi.org/10.2190/NLG4-MC90-78E6-XV80
McGivney, S. A., Mulvihill, M., & Taylor, B. (1994). Validating the GDS depression screen in the nursing home. Journal of the American geriatrics society, 42(5), 490-492. doi: https://doi.org/10.1111/j.1532-5415.1994.tb04969.x
Nikmat, A. W., Hawthorne, G., & Al-Mashoor, S. H. (2015). The comparison of quality of life among people with mild dementia in nursing home and home care—a preliminary report. Dementia, 14(1), 114-125. doi: https://doi.org/10.1177/1471301213494509
OECD. (2017). Health at a Glance 2017. Retrieved May 16, 2020, from https://www.oecd-ilibrary.org/docserver/health_glance-2017-en.pdf?expires=158 9593314&id=id&accname=guest&checksum=1C789BB02278EC9F63AC175803 0597E0
Ogihara, Y. (2017). Temporal changes in individualism and their ramification in Japan: Rising individualism and conflicts with persisting collectivism. Frontiers in psychology, 8, 695. doi: https://doi.org/10.3389/fpsyg.2017.00695
Olsen, C., Pedersen, I., Bergland, A., Enders-Slegers, M. J., Jøranson, N., Calogiuri, G., & Ihlebæk, C. (2016). Differences in quality of life in home-dwelling persons and nursing home residents with dementia–a cross-sectional study. BMC geriatrics, 16(1), 137. doi: https://doi.org/10.1186/s12877-016-0312-4
Pallant, J. F., & Reid, C. (2014). Measuring the positive and negative aspects of the caring role in community versus aged care setting. Australasian journal on ageing, 33(4), 244-249. doi: https://doi.org/10.1111/ajag.12046
Papastavrou, E., Kalokerinou, A., Papacostas, S. S., Tsangari, H., & Sourtzi, P. (2007). Caring for a relative with dementia: family caregiver burden. Journal of advanced nursing, 58(5), 446-457. doi: https://doi.org/10.1111/j.1365-2648.2007.04250.x
Peacock, S., Forbes, D., Markle-Reid, M., Hawranik, P., Morgan, D., Jansen, L., ... & Henderson, S. R. (2010). The positive aspects of the caregiving journey with dementia: Using a strengths-based perspective to reveal opportunities. Journal of applied gerontology, 29(5), 640-659. doi: https://doi.org/10.1177/0733464809341471
Prince, M., Comas-Herrera, A., Knapp, M., Guerchet, M., & Karagiannidou, M. (2016). World Alzheimer report 2016: improving healthcare for people living with dementia: coverage, quality and costs now and in the future.
Quinn, C., Nelis, S. M., Martyr, A., Victor, C., Morris, R. G., Clare, L., & IDEAL Study Team. (2019). Influence of positive and negative dimensions of dementia caregiving on caregiver well-being and satisfaction with life: Findings from the IDEAL Study. The American journal of geriatric psychiatry, 27(8), 838-848. doi: https://doi.org/10.1016/j.jagp.2019.02.005
Quinn, C., & Toms, G. (2019). Influence of positive aspects of dementia caregiving on caregivers’ well-being: A systematic review. The gerontologist, 59(5), e584-e596. doi: https://doi.org/10.1093/geront/gny168
Riffin, C., Van Ness, P. H., Wolff, J. L., & Fried, T. (2019). Multifactorial examination of caregiver burden in a national sample of family and unpaid caregivers. Journal of the American Geriatrics Society, 67(2), 277-283. doi: https://doi.org/10.1111/jgs.15664
Roff, L. L., Burgio, L. D., Gitlin, L., Nichols, L., Chaplin, W., & Hardin, J. M. (2004). Positive aspects of Alzheimer's caregiving: The role of race. The journals of gerontology series B: Psychological Sciences and Social Sciences , 59(4), P185-P190. doi: https://doi.org/10.1093/geronb/59.4.P185
Roth, D. L., Dilworth-Anderson, P., Huang, J., Gross, A. L., & Gitlin, L. N. (2015). Positive aspects of family caregiving for dementia: Differential item functioning by race. Journals of Gerontology Series B: Psychological Sciences and Social Sciences, 70(6), 813-819. doi: https://doi.org/10.1093/geronb/gbv034
Scott, C. B., Clay, O. J., Epps, F., Cothran, F. A., & Williams, I. C. (2018). Associations of knowledge of Alzheimer’s disease and memory loss and employment status with burden in African American and Caucasian family caregivers. Dementia, 1471301218788147. doi: https://doi.org/10.1177/1471301218788147
Sinha, P., Desai, N. G., Prakash, O., Kushwaha, S., & Tripathi, C. B. (2017). Caregiver burden in Alzheimer-type dementia and psychosis: A comparative study from India. Asian journal of psychiatry, 26, 86-91. doi: https://doi.org/10.1016/j.ajp.2017.01.002
Siow, J. Y. M., Chan, A., Østbye, T., Cheng, G. H. L., & Malhotra, R. (2017). Validity and reliability of the positive aspects of caregiving (PAC) scale and development of its shorter version (S-PAC) among family caregivers of older adults. The gerontologist, 57(4), e75-e84. doi: https://doi.org/10.1093/geront/gnw198
Tarlow, B. J., Wisniewski, S. R., Belle, S. H., Rubert, M., Ory, M. G., & Gallagher-Thompson, D. (2004). Positive aspects of caregiving: Contributions of the REACH project to the development of new measures for Alzheimer’s caregiving. Research on aging, 26(4), 429-453. doi: https://doi.org/10.1177/0164027504264493
Tay, K. C. P., Seow, C. C. D., Xiao, C., Lee, H. M. J., Chiu, H. F., & Chan, S. W. C. (2016). Structured interviews examining the burden, coping, self-efficacy, and quality of life among family caregivers of persons with dementia in Singapore. Dementia, 15(2), 204-220. doi: https://doi.org/10.1177/1471301214522047
Vaingankar, J. A., Chong, S. A., Abdin, E., Picco, L., Jeyagurunathan, A., Zhang, Y., ... & Subramaniam, M. (2016). Care participation and burden among informal caregivers of older adults with care needs and associations with dementia. International psychogeriatrics, 28(2), 221-231. doi: https://doi.org/10.1017/S104161021500160X
Wancata, J., Alexandrowicz, R., Marquart, B., Weiss, M., & Friedrich, F. (2006). The criterion validity of the Geriatric Depression Scale: a systematic review. Acta psychiatrica scandinavica, 114(6), 398-410. doi: https://doi.org/10.1111/j.1600-0447.2006.00888.x
Ware Jr, J. E., & Gandek, B. (1998). Methods for testing data quality, scaling assumptions, and reliability: the IQOLA Project approach. Journal of clinical epidemiology, 51(11), 945-952. doi: https://doi.org/10.1016/S0895-4356(98)00085-7
Yu, H., Wang, X., He, R., Liang, R., & Zhou, L. (2015). Measuring the caregiver burden of caring for community-residing people with Alzheimer’s disease. PLoS One, 10(7), e0132168. doi: https://doi.org/10.1371/journal.pone.0132168
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