References
- Acton, G.J., & Wright, K.B. (2000). Self-transcendence and family caregivers of adults with dementia. Journal of Holistic Nursing, 18(2), 143–158.
- Adams, B.M., Aranda, M.P., Kemp, B.J., & Takagi, K. (2002). Ethnic and gender differences in distress among Anglo American, African-American, Japanese-American and Mexican-American spousal caregivers of persons with dementia. Journal of Clinical Geropsychology, 8(4), 279–301. doi:10.1023/A:1019627323558
- Allison, P.D. (Ed.). (2002). Missing data. New York, NY: Sage.
- Alzheimer's Association. (2015). 2015 Alzheimer's disease facts and figures. Retrieved from https://www.alz.org/facts/downloads/facts_figures_2015.pdf
- Aranda, M., & Knight, B. (1997). The influence of ethnicity and culture on the caregiver stress and coping process: A sociocultural review and analysis. The Gerontologist, 37(3), 342–354.
- Archbold, P., Stewart, B., Greenlick, M., & Harvath, T. (1990). Mutuality and preparedness as predictors of caregiver role strain. Research in Nursing & Health, 13(6), 375–384. doi:10.1002/nur.4770130605
- Barber, C.E., & Vega, L.D. (2004). Ethnic differences in the experience of filial caregiving: A comparison of Hispanic and non-Hispanic white caregivers in Colorado. Southwest Journal on Aging, 19, 33–54.
- Barrera, M., Sandler, I.M., & Ramsay, T.B. (1981). Preliminary development of a scale of social support: Studies on college students. American Journal of Community Psychology, 9, 435–446.
- Basu, R., Hochhalter, A.K., & Stevens, A.B. (2015). The impact of the REACH II intervention on caregivers' perceived health. Journal of Applied Gerontology, 34(5), 590–608. doi:10.1177/0733464813499640
- Belle, S.H., Burgio, L., Burns R., Coon, D., Czaja, S.J., Gallagher-Thompson, D., ... Zhang, S. (2006). Enhancing the quality of life of dementia caregivers from different ethnic or racial groups: A randomized, controlled trial. Annals of Internal Medicine, 145, 727–738. doi:10.7326/0003-4819-145-10-200611210-00005
- Brodaty, H., & Donkin, M. (2009). Family caregivers of people with dementia. Dialogues of Clinical Neuroscience, 11(2), 217–228.
- Brodaty, H., & Luscombe, G. (1998). Psychological morbidity in caregivers is associated with depression in patients with dementia. Alzheimer Disease & Associated Disorders, 12(2), 62–70. doi:10.1097/00002093-199806000-00002
- Butcher, H., Holkup, P., & Buckwalter, K. (2001). The experience of caring for a family member with Alzheimer's disease. Western Journal of Nursing Research, 23(1), 33–55. doi:10.1177/019394590102300104
- Coakes, S.J. (2005). SPSS: Analysis without anguish: Version 12.0 for Windows. Sydney: Australia: John Wiley & Sons.
- Davis, C.G., & Morgan, M.S. (2008). Finding meaning, perceiving growth, and acceptance of tinnitus. Rehabilitation Psychology, 53(2), 128–138. doi:10.1037/0090-5550.53.2.128
- Dilworth-Anderson, P., Burton, L., & Boulin-Johnson, L. (1993). Reframing theories for understanding race, ethnicity, and families. In P.G. Boss, W.J. Doherty, R. LaRossa, W.R. Schumm, & S.K. Steinmetz (Eds.), Sourcebook of family theories and methods: A contextual approach (pp. 627–649). New York, NY: Plenum Press.
- Fleury, J., & Lee, S.M. (2006). The social ecological model and physical activity in African American women. American Journal of Community Psychology, 37(1–2), 129–140. doi:10.1007/s10464-005-9002-7
- Gaugler, J., Davey, A., Pearlin, L., & Zarit, S. (2000). Modeling caregiver adaptation over time: The longitudinal impact of behavior problems. Psychology and Aging, 15(3), 437–450. doi:10.1037/0882-7974.15.3.437
- Hair, J.F., Anderson, R.E., Tatham, R.L., & Black, W.C. (1998). Multivariate data analysis (5th ed.). Upper Saddle River, NJ: Prentice-Hall International.
- Haley, W., Levine, E., Brown, S., & Bartolucci, A. (1987). Stress, appraisal, coping, and social support as predictors of adaptational outcome among dementia caregivers. Psychology and Aging, 2(4), 323–330. doi:10.1037//0882-7974.2.4.323
- Haley, W., Roth, D., Coleton, M., Ford, G., West, C., Collins, R., & Isobe, T. (1996). Appraisal, coping, and social support as mediators of well-being in black and white family caregivers of patients with Alzheimer's disease. Journal of Consulting and Clinical Psychology, 64(1), 121–129. doi:10.1037/0022-006X.64.1.121
- Harwood, D.G., Barker, W.W., Ownby, M.B., Aguero, H., & Ranjan, D. (2000). Predictors of positive and negative appraisal among Cuban American caregivers of Alzheimer's disease patients. International Journal of Geriatric Psychiatry, 15(6), 481–487. doi:10.1002/1099-1166(200006)15:6<481::AID-GPS984>3.0.CO;2-J
- Hilgeman, M.M., Durkin, D.W., Sun, F., DeCoster, J., Allen, R.S., Gallagher-Thompson, D., & Burgio, L.D. (2009). Testing a theoretical model of the stress process in Alzheimer's caregivers with race as a moderator. Gerontologist, 49, 248–261. doi:10.1093/geront/gnp015
- Hinrichsen, G., & Ramirez, M. (1992). Black-and-white dementia caregivers: A comparison of their adaptation, adjustment, and service utilization. The Gerontologist, 32(3), 375–381. doi:10.1093/geront/32.3.375
- Knight, B., & McCallum, T. (1998). Heart rate reactivity and depression in African-American and white dementia caregivers: Reporting bias or positive coping? Aging & Mental Health, 2(3), 212–221. doi:10.1080/13607869856696
- Kramer, B. (1997). Gain in the caregiving experience: Where are we? What next? The Gerontologist, 37(2), 218–232. doi:10.1093/geront/37.2.218
- Krause, N. (1995). Negative interaction and satisfaction with social support among older adults. Journal of Gerontology: Psychological Sciences, 50B, 59–73.
- Lazarus, R.S., & Folkman, S. (1984). Stress, appraisal, and coping. New York, NY: Springer.
- Lee, Y.R., & Sung, K.T. (1998). Cultural influences on caregiving burden: Cases of Koreans and Americans. International Journal of Aging & Human Development, 46(2), 125–141. doi:10.2190/PM2C-V93R-NE8H-JWGV
- Levkoff, S., & Sanchez, H. (2003). Lessons learned about minority recruitment and retention from the centers on minority aging and health promotion. The Gerontologist, 43(1), 18–26.
- Lubben, J. (1988). Assessing social networks among elderly populations. Family & Community Health, 11(3), 42–52.
- McLeroy, K.R., Bibeau, D., Steckler, A., & Glanz, K. (1988). An ecological perspective on health promotion programs. Health Education Quarterly, 15, 351–377.
- Mindel, C., & Wright, R. (1982). The use of social-services by black and white elderly: The role of social support systems. Journal of Gerontological Social Work, 4(3–4), 107–125. doi:10.1300/J083V04N03_10
- Mintzer, J.E., Rubert, M.P., & Herman, K.C. (1994). Caregiving for Hispanic Alzheimer's disease patients: Understanding the problem. American Journal of Geriatric Psychiatry, 2, 32–38.
- Motenko, A. (1989). The frustrations, gratifications, and well-being of dementia caregivers. The Gerontologist, 29(2), 166–172.doi:10.1093/geront/29.2.166
- Mui, A. (1992). Caregiver strain among black and white daughter caregivers: A role-theory perspective. The Gerontologist, 32(2), 203–212. doi:10.1093/geront/32.2.203
- Nakagawa, Y., & Nasu, S. (2011). Association between components of family caregivers' sense of burden and types of paid care services provided in Japan. Aging & Mental Health, 15, 687–701. doi:10.1080/13607863.2011.562181
- Nápoles, A.M., Chadiha, L., Eversley, R., & Moreno-John, G. (2010). Developing culturally sensitive dementia caregiver interventions: Are we there yet? American Journal of Alzheimer's Disease, 25(5), 389–406. doi:10.1177/1533317510370957
- O'Brien, R.M. (2007). A caution regarding rules of thumb for variance inflation factors. Quality & Quantity, 41(5), 673–690. doi:10.1007/s11135-006-9018-6
- Ory, M.G., Yee, J.L., Tennstedt, S.L., & Schulz, R. (2000). The extent and impact of dementia care: Unique challenges experienced by family caregivers. In R. Schulz (Ed.), Handbook of dementia caregiving: Evidence-based interventions for family caregivers (pp. 1–32). New York, NY: Springer.
- Pallant, J. (2001). SPSS survival manual: A step by step guide to data analysis using SPSS for Windows (Version 10). Buckingham, PA: Open University Press.
- 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:10.1177/0733464809341471
- Pearlin, L., Mullan, J., Semple, S., & Skaff, M. (1990). Caregiving and the stress process: An overview of concepts and their measures. The Gerontologist, 30(5), 583–594. doi:10.1093/geront/30.5.583
- Perry, J. (2002). Wives giving care to husbands with Alzheimer's disease: A process of interpretive caring. Research in Nursing & Health, 25(4), 307–316. doi:10.1002/nur.10040
- Picot, S.J. (1994). Choice and social exchange theory and the rewards of African American caregivers. Journal of National Black Nurses' Association: JNBNA, 7(2), 29–40.
- Picot, S.J. (1995). Rewards, costs, and coping of African-American caregivers. Nursing Research, 44(3), 147–152.
- Picot, S.J., Debanne, S.M., Namazi, K.H., & Wykle, M.L. (1997). Religiosity and perceived rewards of Black and White caregivers. The Gerontologist, 37, 89–101. doi:10.1093/geront/37.1.89
- Pinquart, M., & Sörensen, S. (2005). Ethnic differences in stressors, resources, and psychological outcomes of family caregiving: A meta-analysis. The Gerontologist, 45(1), 90–106. doi:10.1093/geront/45.1.90
- Pot, A.M., Zarit, S.H., Twisk, J.W.R., & Townsend, A.L. (2005). Transitions in caregivers' use of paid home help: Associations with stress appraisals and well-being. Psychology and Aging, 20(2), 211–219. doi:10.1037/0882-7974.20.2.211
- Quayhagen, M.P., & Quayhagen, M. (1988). Alzheimer's stress: Coping with the caregiving role. The Gerontologist, 28(3), 391–396. doi:10.1093/geront/28.3.391
- Roff, L., Burgio, L., Gitlin, L., Nichols, L., Chaplin, W., & Hardin, J. (2004). Positive aspects of Alzheimer's caregiving: The role of race. Journals of Gerontology Series B: Psychological Sciences and Social Sciences, 59(4), P185–P190. doi:10.1093/geronb/59.4.P185
- Schacke, C.S., & Zank, S.R. (2006). Measuring the effectiveness of adult day care as a facility to support family caregivers of dementia patients. Journal of Applied Gerontology, 25(1), 65–81. doi:10.1177/0733464805284195
- Schafer, J.L., & Graham, J.W. (2002). Missing data: Our view of the state of the art. Psychological Methods, 7(2), 147–177. doi:10.1037/1082-989X.7.2.147
- Schulz, R., Visintainer, P., & Williamson, G. (1990). Psychiatric and physical morbidity effects of caregiving. Journals of Gerontology, 45(5), P181–P191. doi:10.1093/geronj/45.5.P181
- Schulz, R., & Williamson, G.M. (1994). Health effects of caregiving: Prevalence of mental and physical illness in Alzheimer's caregivers. In E. Light, G. Niederehe, & B.D. Lebowitz (Eds.), Stress effects on family caregivers of Alzheimer's patients: Research and interventions (pp. 38–63). New York, NY: Springer.
- Semiatin, A.M., & O'Connor, M.K. (2012). The relationship between self-efficacy and positive aspects of caregiving in Alzheimer's disease caregivers. Aging & Mental Health, 16(6), 683–688. doi:10.1080/13607863.2011.651437
- Sherrell, K., Buckwalter, K., & Morhardt, D. (2001). Negotiating family relationships: Dementia care as a midlife developmental task. Families in Society: The Journal of Contemporary Human Services, 82(4), 383–392.
- Spillman, B.C., & Long, S.K. (2009). Does high caregiver stress predict nursing home entry? Inquiry, 46(2), 140–161.
- Spurlock, J. (1984). Black women in the middle years. In G. Baruch & J. Brooks-Gunn (Eds.), Women in midlife (pp. 150–177). New York, NY: Plenum Press.
- Tabachnick, B.G., & Fidell, L.S. (2001). Using multivariate statistics. Boston, MA: Allyn & Bacon.
- Tarlow, B., Wisniewski, S., Belle, S., Rubert, M., Ory, M., & 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:10.1177/0164027504264493
- Teri, L., Truax, P., Logsdon, R., Uomoto, J., Zarit, S., & Vitaliano, P.P. (1992). Assessment of behavioral problems in dementia: The revised memory and behavior problems checklist (RMBPC). Psychology and Aging, 18, 375–384. doi:10.1037/0882-7974.7.4.622
- Vitaliano, P., Young, H., & Zhang, J. (2004). Is caregiving a risk factor for illness? Current Directions in Psychological Science, 13(1), 13–16. doi:10.1111/j.0963-7214.2004.01301004.x
- Wayman, J.C. (2003). Multiple imputation for missing data: What is it and how can I use it? Paper presented at the Annual Meeting of the American Educational Research Association, Chicago, IL. Retrieved from http://www.csos.jhu.edu/contact/staff/jwayman_pub/wayman_multimp_aera2003.pdf
- Wood, J.B., & Parham, I.A. (1990). Coping with perceived burden: Ethnic and cultural issues in Alzheimer's family caregiving. Journal of Applied Gerontology, 9(3), 325–339. doi:10.1177/073346489000900307
- Zarit, S.H. (2012). Positive aspects of caregiving: More than looking on the bright side. Aging & Mental Health, 16(6), 673–674. doi:10.1080/13607863.2012.692768