Abstract
Families play an important role in the lives of individuals with mental illness. Coping with the strain of shifting roles and multiple challenges of caregiving can have a huge impact. Limited information exists regarding race-related differences in families’ caregiving experiences, their abilities to cope with the mental illness of a loved one, or their interactions with mental health service systems. This study examined race-related differences in the experiences of adults seeking to participate in the National Alliance on Mental Illness Family-to-Family Education Program due to mental illness of a loved one. Participants were 293 White and 107 African American family members who completed measures of problem- and emotion-focused coping, knowledge about mental illness, subjective illness burden, psychological distress, and family functioning. Multiple regression analyses were used to determine race-related differences. African American caregivers reported higher levels of negative caregiving experiences, less knowledge of mental illness, and higher levels of both problem-solving coping and emotion-focused coping, than White caregivers. Mental health programs serving African American families should consider targeting specific strategies to address caregiving challenges, support their use of existing coping mechanisms and support networks, and increase their knowledge of mental illness.
Similar content being viewed by others
References
Alvidrez, J., Snowden, L. R., & Kaiser, D. M. (2008). The experience of stigma among Black mental health consumers. Journal of Health Care for the Poor and Underserved, 19(3), 874–893. doi:10.1353/hpu.0.0058.
Awad, A. G., & Voruganti, L. N. P. (2008). The burden of schizophrenia on caregivers. Pharmacoeconomics, 26(2), 149–162. doi:10.2165/00019053-200826020-00005.
Banks-Wallace, J., & Parks, L. (2004). It’s all sacred: African American women’s perspectives on spirituality. Issues in Mental Health Nursing, 25, 25–45. doi:10.1080/01612840490248911.
Benjamini, Y., & Yekutieli, D. (2001). The control of the false discovery rate in multiple testing under dependency. Annual Statistics, 29, 1165–1188. doi:10.2307/2674075.
Biegel, D. E., Milligan, S. E., Putnam, P. L., & Song, L. (1994). Predictors of burden among lower socioeconomic status caregivers of persons with chronic mental illness. Community Mental Health Journal, 30(5), 473–494. doi:10.1007/BF02189064.
Briggs, H. E., Briggs, A. C., Miller, K. M., & Paulson, R. I. (2011). Combating persistent cultural incompetence in mental health care systems serving African Americans. Best Practices in Mental Health: An International Journal, 7(2), 1–25.
Carver, C. S., Scheier, M. F., & Weintraub, J. K. (1989). Assessing coping strategies: A theoretically based approach. Journal of Personality and Social Psychology, 56, 267–283. doi:10.1037//0022-3514.56.2.267.
Chen, F., & Greenberg, J. S. (2004). A positive aspect of caregiving: The influence of social support on caregiving gains for family members of relatives with schizophrenia. Community Mental Health Journal, 40(5), 423–435. doi:10.1023/B:COMH.0000040656.89143.82.
Cheng, C., & Cheung, M. W. L. (2005). Cognitive processes underlying coping flexibility: Differentiation and integration. Journal of Personality, 73, 859–886.
Connery, L., & Brekke, J. (1999). A home-based family intervention for ethnic minorities with a mentally ill member. Alcoholism Treatment Quarterly, 17(1–2), 149–167. doi:10.1300/J020v17n01_09.
Corrigan, P. W., & Miller, F. E. (2004). Shame, blame and contamination: A review of the impact of mental illness stigma on family members. Journal of Mental Health, 13(6), 537–548. doi:10.1080/09638230400017004.
Cummings, S. M., & MacNeil, G. (2008). Caregivers of older clients with severe mental illness: Perceptions of Burdens and Rewards. Families in Society: The Journal of Contemporary Social Services, 89(1), 51–60. doi:10.1606/1044-3894.3709.
Derogatis, L. R. (2001). Brief symptom inventory BSI-18: Administration scoring and procedures manual. New York, NY: NCS Pearson Inc.
Dixon, L. B., Dickerson, F., Bellack, A. S., Bennett, M., Dickinson, D., Goldberg, R. W., et al. (2010). The 2009 schizophrenia PORT psychosocial treatment recommendations and summary statements. Schizophrenia Bulletin, 36(1), 48–70. doi:10.1093/schbul/sbp115.
Dixon, L., Lucksted, A., Medoff, D. R., Burland, J., Stewart, B., & Murray-Swank, A. (2011). Outcomes of a randomized study of a peer-taught family-to-family education program for mental illness. Psychiatric Services, 62(6), 591–597. doi:10.1176/appi.ps.62.6.591.
Dixon, L., Lucksted, A., Stewart, B., Burland, J., Brown, C. H., & Hoffman, M. (2004). Outcomes of the peer-taught 12-week family to-family education program for severe mental illness. Acta Psychiatrica Scandinavica, 109, 207–215. doi:10.1046/j.0001-690X.2003.00242.x.
Epstein, N. B., Baldwin, L. M., & Bishop, D. S. (1983). The McMaster family assessment device. Journal of Marital and Family Therapy, 9, 171–180. doi:10.1111/j.1752-0606.1983.tb01497.x.
Gerson, R., Davidson, L., Booty, A., Wong, C., McGlashan, T., & Corcoran, C. (2009). Families experience with seeking treatment for early-onset psychosis. Psychiatric Services, 60(6), 812–816. doi:10.1176/appi.ps.60.6.812.
Greer, T. (2007). Measuring coping strategies among African Americans: An exploration of the latent structure of the COPE Inventory. Journal of Black Psychology, 33, 260–278. doi:10.1177/0095798407302539.
Guada, J., Brekke, J. S., Floyd, R., & Barbour, J. (2009). The relationships among perceived criticism, family contact, and consumer clinical and psychosocial functioning for African American consumers with schizophrenia. Community Mental Health Journal, 45(2), 106–116. doi:10.1007/s10597-008-9165-4.
Guada, J., Hoe, M., Floyd, R., Barbour, J., & Brekke, J. S. (2012). How family factors impact psychosocial functioning for African American consumers with schizophrenia. Community Mental Health Journal, 48(1), 45–55. doi:10.1007/s10597-010-9365-6.
Guada, J., Land, H., & Han, J. (2011). An exploratory factor analysis of the burden assessment scale with a sample of African-American families. Community Mental Health Journal, 2(47), 233–242. doi:10.1007/s10597-010-9298-0.
Guarnaccia, P., & Parra, P. (1996). Ethnicity, social status, and families’ experiences of caring for a mentally ill family member. Community Mental Health Journal, 32(3), 243–260. doi:10.1007/BF02249426.
Haley, W. E., Roth, D. L., Coleton, M. I., Ford, G. R., West, C. A. C., Collins, R. P., et al. (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.
Hatchett, S. J., Cochran, D. L., & Jackson, J. S. (1991). Family life. In J. S. Jackson (Ed.), Life in black America (pp. 46–83). Newbury Park, CA: Sage.
Hoe, M., & Brekke, J. S. (2008). Cross-ethnic measurement invariance of the Brief Symptom Inventory for individuals with severe and persistent mental illness. Social Work Research, 32(2), 71–78.
Horwitz, A. V., & Reinhard, S. C. (1995). Ethnic differences in caregiving duties and burdens among parents and siblings of persons with severe mental illnesses. Journal of Health and Social Behavior, 36(2), 138–150. doi:10.2307/2137221.
Kessler, R. C., Aguilar-Gaxiola, S., Alonso, J., Chatterji, S., Lee, S., & Wang, P. S. (2008). The global burden of mental disorders: An update from the who world mental health surveys. Epidemiologia e Psichiatria Sociale, 18(1), 23–33.
Knight, B. G., Silverstein, M. L., McCallum, T. J., & Fox, L. S. (2000). A sociocultural stress and coping model for mental health outcomes among African American caregivers in southern California. Journal of Gerontology: Psychological Sciences, 55B(3), 142–150. doi:10.1093/geronb/55.3.P142.
Koren, P., DeChillo, N., & Friesen, B. (1992). Measuring empowerment in families whose children have emotional disorders: A brief questionnaire. Rehabilitation Psychology, 37, 305–321.
Lazaurus, R. S., & Folkman, S. (1984). Stress, appraisal, and coping. New York: Springer.
Link, B. G., Mirotznik, J., & Cullen, F. T. (1991). The effectiveness of stigma coping orientations: Can negative consequences of mental illness labeling be avoided? Journal of Health and Social Behavior, 32(3), 302–320. doi:10.2307/2136810.
Lucksted, A., Medoff, D., Burland, J., Stewart, B., Fang, L. J., Brown, C., et al. (2013). Sustained outcomes of a peer-taught family education program on mental illness. Acta Psychiatrica Scandinavica, 127(4), 279–286. doi:10.1111/j.1600-0447.2012.01901.x.
Lucksted, A., Stewart, B., & Forbes, C. B. (2008). Benefits and changes for family to family graduates. American Journal of Community Psychology, 42(1–2), 154–166. doi:10.1007/s10464-008-9195-7.
Marcus, S. M., Medoff, D., Fang, L. J., Weaver, J., Duan, N., Lucksted, A., et al. (2013). Generalizability in the Family-to-Family Education Program randomized waitlist-control trial. Psychiatric Services, 64(8), 754–763. doi:10.1176/appi.ps.002912012.
Mattis, J. S. (2002). Religion and spirituality in the meaning-making and coping experiences of African American women: A qualitative analysis. Psychology of Women Quarterly, 26, 309–321. doi:10.1111/1471-6402.t01-2-00070.
Mattis, J. S. (2004). Spirituality and religion in African American life. In R. L. Jones (Ed.), Black psychology (4th ed., pp. 93–115). California: Cobb & Henry.
McCubbin, M. A., McCubbin, H. I., & Thompson, A. I. (1996). Family problem-solving communication (FBSC). In H. I. McCubbin, A. I. Thompson, & M. A. McCubbin (Eds.), Family assessment: Resiliency, coping and adaptation (inventories for research and practice). Madison: University of Wisconsin.
Neighbors, H. W., & Jackson, J. S. (1984). The use of informal and formal help: Four patterns of illness behavior in the black community. American Journal of Community Psychology, 12(6), 629–644. doi:10.1007/BF00922616.
Nguyen, H. T., Kitner-Triolo, M., Evans, M. K., & Zonderman, A. B. (2004). Factorial invariance of the CES-D in low socioeconomic status African Americans compared with a nationally representative sample. Psychiatry Research, 126, 177–187. doi:10.1016/j.psychres.2004.02.004.
Pickard, J., Inoue, M., Chadiha, L., & Johnson, S. (2012). The relationship of social support to African American caregivers’ help-seeking for emotional problems. Social Service Review, 85, 247–266. doi:10.1086/660068.
Pickett, S., Vraniak, D., Cook, J., & Cohler, B. (1993). Strength in adversity: Blacks bear burden better than Whites. Professional Psychology: Research and Practice, 24(4), 460–467. doi:10.1037/0735-7028.24.4.460.
Radloff, L. S. (1977). The CES-D scale: A self-report depression scale for research in the general population. Applied Psychological Measurement, 1, 385–401. doi:10.1177/014662167700100306.
Radloff, L. S., & Lock, B. Z. (1986). The community mental health assessment survey and the CES-D scale. In M. Weissman, J. Meyers, & C. Ross (Eds.), Community surveys. New Brunswick, NJ: Rutgers University Press.
Rozario, P. A., & Menon, N. (2010). An examination of the measurement adequacy of the CES-D among African American women family caregivers. Psychiatry Research, 179, 107–112. doi:10.1016/j.psychres.2010.06.022.
Saunders, J. C. (2003). Families living with severe mental illness: A literature review. Issues in Mental Health Nursing, 24, 175–198. doi:10.1080/01612840305301.
Sawin, K. J., Harrigan, M. P., & Woog, P. (1995). Measures of family functioning for research and practice. New York: Springer.
Schulze, B., & Rössler, W. (2005). Caregiver burden in mental illness: review of measurement, findings and interventions in 2004–2005. Current Opinion in Psychiatry, 18(6), 684–689.
Sideridis, G. D. (2006). Coping is not an ‘either’ ‘or’: The interaction of coping strategies in regulating affect, arousal and performance. Stress and Health: Journal of the International Society for the Investigation of Stress, 22(5), 315–327. doi:10.1002/smi.1114.
Snowden, L. R. (1998). Racial differences in informal help seeking for mental health problems. Journal of Community Psychology, 26(5), 429–438. doi:10.1002/(SICI)1520-6629(199809)26:5<429:AID-JCOP3>3.3.CO;2-K.
Solomon, P., & Draine, J. (1995a). Subjective burden among family members of mentally ill adults: Relation to stress, coping, and adaptation. American Journal of Orthopsychiatry, 65, 419–427.
Solomon, P., & Draine, J. (1995b). Adaptive coping among family members of persons with serious mental illness. Psychiatry Services, 46(11), 1156–1160.
Stueve, A., Vine, P., & Struening, E. L. (1997). Perceived burden among caregivers of adults with serious mental illness: Comparison of Black, Hispanic, and White families. American Journal of Orthopsychiatry, 67(2), 199–209. doi:10.1037/h0080223.
Szmukler, G., Burgess, P., Herrman, H., Benson, A., Colusa, S., & Bloch, S. (1996). Caring for relatives with serious mental illness: The development of the experience of caregiving inventory. Social Psychiatry and Psychiatric Epidemiology, 31, 37–148. doi:10.1007/BF00785760.
Taylor, R. J., & Chatters, L. M. (1988). Church members as a source of informal social support. Review of Religious Research, 30, 193–203. doi:10.2307/3511355.
Taylor, R. J., Chatters, L. M., & Celious, A. (2003). Extended family households among black Americans. African American Research Perspectives, 1, 133–151.
Taylor, R. J., Chatters, L. M., Hardison, C. B., & Riley, A. (2001). Informal social support networks and subjective well-being among African Americans. Journal of Black Psychology, 27(4), 439–463. doi:10.1177/0095798401027004004.
Tessler, R., & Gamache, G. (1993). Family Experiences Interview Schedule (FEIS). In: The toolkit on evaluating family experiences with severe mental illness. Cambridge, Mass, Human Services Research Institute, Evaluation Center, 1993. Available at www.hsri.org.
Utsey, S. O., Bolden, M. A., Williams, O, I. I. I., Lee, A., Lanier, Y., & Newsome, C. (2007). Spiritual well-being as a mediator of the relation between culture-specific coping and quality of life in a community sample of African Americans. Journal of Cross-Cultural Psychology, 38(2), 123–136. doi:10.1177/0022022106297296.
Woodward, A. T. (2011). Discrimination and help-seeking: Use of professional services and informal support among African Americans, black Caribbeans, and non-Hispanic whites with a mental disorder. Race and Social Problems, 3(3), 146–159.
Young, J. L., Griffith, E. E. H., & Williams, D. R. (2003). The integral role of pastoral counseling by African–American clergy in community mental health. Psychiatric Services, 54(5), 688–692.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Smith, M.E., Lindsey, M.A., Williams, C.D. et al. Race-Related Differences in the Experiences of Family Members of Persons with Mental Illness Participating in the NAMI Family to Family Education Program. Am J Community Psychol 54, 316–327 (2014). https://doi.org/10.1007/s10464-014-9674-y
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10464-014-9674-y