Abstract
Graduate public health courses that address social and behavioral dimensions of health emphasize the examination of forces beyond the individual that impact the community and the individual’s health and health behavior. A goal of these courses is to shift students’ focus from a traditional orientation on individual health to a population health perspective. In line with the goal of public health to understand what places people “at risk for risks” (Link & Phelan, 1995, p. 80), these courses look upstream at structural influences that ultimately impact the individual’s biology either directly or indirectly through behavior. Some researchers in this field have argued that these upstream influences are the predominant or fundamental determinants of health (Link & Phelan). With this contextual, environmental orientation, the content of these courses share much in common with the current approach to understanding disability. However, there remains little overlap or integration between the content of courses examining social and behavioral dimensions of health and disability studies. It is therefore important that disability content be infused in courses that cover social and behavioral dimensions of health. It is the goal of this chapter to address how the understanding of social and behavioral dimensions of health can be improved by integrating disability content. First, an overview of the typical content of these courses is provided, followed by a discussion of disability-related research and finally, recommendations are offered on how to integrate the two fields.
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References
Addis, M.E. & Mahalik, J.R. (2003). Men, masculinity, and the contexts of help seeking. American Psychologist, 58(1), 5–14.
Adler, N.E., Boyce, T., Chesney, M.A., Cohen, S., Follman, S., Kahn, R.L., & Syme, S.L. (1994). Socioeconomic status and health: The challenge of the gradient. American Psychologist, 49, 15–24.
Albert, S.M., Im, A., & Raveis, V.H. (2002). Public health and the second 50 years of life. American Journal of Public Health, 92, 1214–1216.
Albrecht, G. (1992). The disability business: Rehabilitation in America. Newbury Park: Sage.
Anderson N.B. & Armstead, C.A. (1995). Toward understanding the association of socioeconomic status and health: A new challenge for the biopyschosocial approach. Psychosomatic Medicine, 57, 213–225.
Association of Schools of Public Health. (2006). Master’s degree in public health core competency development project version 2.3. Retrieved February 1, 2010, from http://www.asph.org/document.cfm?page=851
Beale, F. (1970). Double jeopardy: To be black and female. In T. Cade (Ed.), The black woman (pp. 90–100). New York: New American Library.
Berkman, L.F. (1995). The role of social relations in health promotion. Psychosomatic Medicine, 57, 245–254.
Berkman, L.F. & Glass, T. (2000) Social integration, social networks, social support, and health. In L.F. Berkman & I. Kawachi (Eds.), Social epidemiology (pp. 174–190). New York: Oxford University Press.
Berkman, L.F. & Kawachi, I. (Eds.). (2000). Social epidemiology. New York: Oxford University Press.
Bickenbach, J.E., Chatterji, S., Badley, E.M., & Ustun, T.B. (1999). Models of disablement, universalism and the international classification of impairments, disabilities and handicaps. Social Science & Medicine, 48, 1173–1187.
Bradsher, J.E. (1995). Disability among racial and ethnic groups. Disability Statistics Abstract, 10, 1–4.
Brawarsky, P., Brooks, D.R. Wilber, N., Gertz, Jr, R.E. & Klein Walker, D. (2002). Tobacco use among adults with disabilities in Massachusetts. Tobacco Control, 11(Suppl II), ii29–ii33.
Braithwaite, D.O. & Eckstein, N.J. (2003). How people with disabilities communicatively manage assistance: Helping as instrumental social support. Journal of Applied Communication Research, 31(1), 1–26.
Brown, S.C. (2001). Methodological paradigms that shape disability research. In G.L. Albrecht, K.D. Seelman, & M. Bury (Eds.), Handbook of disability studies (pp. 145–170). Thousand Oaks: Sage.
Bullock, C. & Devereux, P. (2003). Examining social support in people with disabilities. Unpublished manuscript.
Chase, B.W., Cornille, T.A., & English, R.W. (2000). Life satisfaction among persons with spinal cord injuries. Journal of Rehabilitation, 66(3), 14–20.
Coreil, J., Bryant, C.A., & Henderson, J.N. (2001). Social and behavioral foundations of public health. Thousand Oaks, CA: Sage.
Crews, J.E. & Smith, S.M. (2003) Public health and aging. American Journal of Public Health, 93(5), 700–701.
Crosse, S.B., Kaye, E., & Ratnofsky, A.C. (1993). A report on the maltreatment of children with disabilities. Washington: Office on Child Abuse and Neglect.
Decker, S.D. & Schultz, R. (1985). Correlates of life satisfaction in middle-aged and elderly spinal cord-injured persons. The American Journal of Occupational Therapy, 39, 740–745.
Devereux, P., Bullock, C., Bargmann, J., & Kyriakou, M. (2003). People with disabilities who receive high levels of support: What’s working? Unpublished manuscript.
Devereux, P.G., Bullock, C.C., Bargmann-Losche, J. & Kyriakou, M. (2005). Maintaining Support in People with Paralysis: What works?. Qualitative Health Research, 15(10), 1360-1376.
Disability Statistics Center. (n.d.) How often do people with disabilities participate in entertainment and socializing? Retrieved May 27, 2003, from http://www.dsc.ucsf.edu/
Dohrenwend, B.P., Levav, I., Shrout, P.E., & Schwartz, S. (1992). Socioeconomic status and psychiatric disorders: The causation-selection issue. Science, 255(5047), 946–952.
Dowling, M., & Dolan, L. (2001). Families with children with disabilities: Inequalities and the social model. Disability & Society, 16(1), 21 – 35.
Durkheim, E. (1897). Suicide: A study in sociology. Glencoe: Free Press.
Elliott, T.R. & Shewchuk, R.M. (1995). Social support and leisure activities following severe physical disability: Testing the mediating effects of depression. Basic and Applied Social Psychology, 16(4), 471–487.
Fadem, P., Minkler, M., Perry, M., Blum, K., Moore, L., & Rogers, J. (2003). Ethical challenges in community based participatory research: A case study from the San Francisco Bay Area disability community. In M. Minkler & N. Wallerstein (Eds.), Community-based participatory research for health (pp. 242–262). San Francisco: Jossey-Bass
Faul M, Xu L, Wald MM, & Coronado VG. (2010). Traumatic brain injury in the United States: Emergency department visits, hospitalizations, and deaths. Atlanta (GA): Centers for Disease Control and Prevention, National Center for Injury Prevention and Control.
Fontana, A., Kerns, R., Rosenberg, R., & Colonese, K. (1989). Support, stress, and recovery from coronary heart disease: A longitudinal causal model. Health Psychology, 8, 175–193.
Fuhrer, M.J., Rintala, D.H., Hart, K.A., Clearman, R., & Young, M.E. (1993). Depressive symptomatology in persons with spinal cord injury who reside in the community. Archives of Physical Medicine and Rehabilitation, 74, 255–260.
Fujiura, G.T., Fitzsimons N., Marks B., & Chicoine, B. (1997). Predictors of BMI among adults with Down syndrome: the social context of health promotion. Research in Developmental Disabilities, 18(4), 261–274.
Fulcher, G. (1989). Disabling policies? London: Falmer Press.
Gartner, A. & Joe, T. (Eds.). (1987). Images of the disabled, disabling images. New York: Praeger.
Gilson, S.F., DePoy, E., & MacDuffie, H. (2002). Disability and social work education: A multitheoretical approach. In S.F. Gilson, E. DePoy, H. MacDuffie, & K Meyershon (Eds.), Integrating disability content in social work education: A curriculum resource (pp. 1–8). Alexandria: Council on Social Work Education.
Gleason, M.E.J., Iida, M., Bolger, N., & Shrout, P.E. (2003). Daily supportive equity in close relationships. Personality and Social Psychology Bulletin, 29(8), 1036–1045.
Goffman, E. (1963). Stigma: Notes on the management of spoiled identity. NY: Prentice-Hall.
Goggin, G., & Newell, C. (2003). Digial disability: The social construction of disability in new media. Lanhan, MD: Rowman & Littlefied.
Grant, B.F., Hasin, D.S., Chou, S.P., Stinson, F.S., & Dawson, D.A. (2004). Nicotine dependence and psychiatric disorders in the United States: Results from the National Epidemiologic Survey on Alcohol and Related Conditions. Archives of General Psychiatry, 61, 1107–1115.
Hahn, H. (1988). The politics of physical differences: Disability and discrimination. Journal of Social Issues, 44, 39.
Helman, C.G. (2000). Culture, health and illness (4th ed). Oxford: Butterworth-Heinemann.
Hendershot, G., Colpe, L., & Hunt, P. (1999). Participation of persons with disabilities in household surveys: A conceptual framework for empirical investigation. Unpublished Manuscript.
Institute of Medicine. (2001). Health and behavior: The interplay of biological, behavioral, and societal influences. Washington: National Academy Press.
Jans, L., & Stoddard, S. (1999). Chartbook on women and disability in the United States. Washington: National Institute on Disability and Rehabilitation Research.
Kennedy, J. & Minkler, M. (1998). Disability theory and public policy: Implications for critical gerontology. International Journal of Health Services, 28(4), 757–776.
Kelly, M.P. Disability and community: A sociological approach. In G.L. Albrecht, K.D. Seelman, & M. Bury (Eds.), Handbook of disability studies (pp. 396–411). Thousand Oaks: Sage.
King, G. & Williams, D.R. (1995). Race and health: A multidimensional approach to African-American health. In B.C. Amick, S. Levine, A.R. Tarlov, & D.C. Walsh (Eds.), Society and health (pp. 93–130). New York: Oxford University Press.
Krieger, N. (2000). Discrimination and health. In L.F. Berkman & I. Kawachi (Eds.), Social epidemiology (pp. 36–75). New York: Oxford University Press.
Krieger, N. (2001). A glossary for social epidemiology. Journal of Epidemiology and Community Health, 55, 693–700.
LaPlante, M.P. & Carlson, D. (1996). Disability in the United States: Prevalence and causes, 1992. Disability Statistics Report, 7. Washington: National Institute on Disability and Rehabilitation Research.
Lenhart, A., Horrigan, J., Rainie, L., Allen, K., Boyce, A., Madden, M., et al. (2003). The ever-shifting internet population: A new look at Internet access and the digital divide. The Pew Internet & American Life Project. Retrieved September 5, 2003, from http://www.pewinternet.org/reports/toc.asp?Report=88
Lepore, S.J., Evans, G.W., & Schnieder, M. (1991). Dynamic role of social support in the link between chronic distress and psychological distress. Journal of Personality and Social Psychology, 61, 899–909.
Link, B.G. & Phelan, J. (1995). Social conditions as fundamental causes of disease [extra issue]. Journal of Health and Social Behavior, 35, 80–94.
Linton, S. (1998). Disability studies/not disability studies. Disability & Society, 13(4), 525–540.
Lollar D. (2000). Plenary session discussion on the disability chapter of healthy people 2010 and conference participants responses. In G.W. White, A.D. Branstetter, & T. Seekins (Eds.), Secondary conditions among people with disabilities from minority cultures; proceedings and recommendations of a working conference. Lawrence: Research and Training Center on Independent Living; University of Kansas.
Lollar, D.J. (2001). Public health trends in disability: Past, present, and future. In G.L. Albrecht, K.D. Seelman, & M. Bury (Eds.), Handbook of disability studies (pp. 754–771). Thousand Oaks: Sage.
Lollar, D.J. & Crews, J.E. (2003). Redefining the role of public health in disability. Annual Review of Public Health, 24, 195–208.
Lupton, D. (2000) The social construction of medicine and the body. In G.L. Albrecht, R. Fitzpatrick, & S.C. Scrimshaw (Eds.), Handbook of social studies in health and medicine (pp. 50–63). London: Sage.
Lynch, J.W., Kaplan, G.A., & Shema, S.J. (1997). Cumulative impact of sustained economic hardship on physical, cognitive, psychological and social functioning. New England Journal of Medicine, 337, 1889–1895.
Mackenbach, J.P., Borsboom, G.J., Nusselder, W.J., Looman, C.W., & Schrijvers, C.T. (2001). Determinants of levels of changes of physical functioning in chronically ill persons: Results from the GLOBE study. Journal of Epidemiology and Community Health, 55(9), 631–638.
Marmot, M. (2000). Multilevel approaches to understanding social determinants. In L.F. Berkman & I. Kawachi (Eds.), Social epidemiology (pp. 349–367). New York: Oxford University Press.
McKinlay, J.B., & Marceau, L.D. (2000). To boldly go… American Journal of Public Health, 90(1), 25–33.
McLeroy, K.R., DeVillis, R., DeVillis, B., et al. (1984). Social support and physical recovery in a stroke population. Journal of Social and Personal Relations, 1, 395–413.
Melleck, D. (1997). Craig Hospital Inventory of Environmental Factors Short Form (CHIEF-SF). Retrieved June 24, 2003, from http://www.tbims.org/combi/chief/index.html
Minkler, M., Fadem, P., Perry, M., Blum, K., Moore, L., & Rogers, J. (2002). Ethical dilemmas in participatory action research: A case study from the disability community. Health Education & Behavior, 29(1), 14–29.
Murphy, C.C., Boyle, C., Schendel, D., Decoufle, P., & Yeargin-Allsop, M. (1998). Epidemiology of mental retardation in children. Mental Retardation and Developmental Disabilities Research Review, 4, 6–13.
National Center for the Dissemination of Disability Research. (1999a). Disability, diversity and dissemination: A review of the literature on topics related to increasing the utilization of rehabilitation research outcomes among diverse consumer groups. Part 1: Theoretical framework. Research Exchange, 4(1). Retrieved May 15, 2003, from http://www.ncddr.org/ du/researchexchange/v04n01/
National Center for the Dissemination of Disability Research (1999b). The socially constructed nature of race, culture, and disability. Research Exchange, 4(1). Retrieved September 26, 2010 from http://www.ncddr.org/products/researchexchange/v04n01/concepts.html
National Center on Birth Defects and Developmental Disabilities. (2001). Healthy people 2010: Chapter 6, vision for the decade: Proceedings and recommendations of a symposium. Atlanta: Centers for Disease Control and Prevention.
National Center on Birth Defects and Developmental Disabilities [NCBDDD] (2003). Healthy People 2010 disability and secondary conditions focus area 6 reports and proceedings. Retrived July 12, 2005 from http://www.cdc.gov/ncbddd/dp
National Organization on Disability. (n.d.). Economic participation. Retrieved August 4, 2003, from http://www.nod.org/economic/
Norris, F.H. & Kaniasty, K. (1996). Received and perceived social support in times of stress: A test of the social support deterioration deterrence model. Journal of Personality and Social Psychology, 71(3), 498–511.
Nosek, M.A., Rintala, D.H., Young, M.E., Foley, C.C., Howland, C., Chanpong, G.F., Rossi, D., Bennett, J., & Meroney, K. (1997). National study of women with physical disabilities. Houston: Baylor College of Medicine.
Oliver, M. (1986). Social policy and disability: Some theoretical issues. Disability, Handicap and Society, 1, 5.
Oliver, M. (1990). The politics of disablement. Basingstoke: Macmillan.
Parsons, J.A., Baum, S., & Johnson, T.P. (2000). Inclusion of disabled populations in social surveys: Review and recommendations. University of Illinois at Chicago: The Survey Research Laboratory.
Post, M.W.M., Ros, W.J.G., & Schrijvers, A.J.P. (1999). Impact of social support on health status and life satisfaction in people with spinal cord injury. Psychology and Health, 14(4), 679–695.
Reis, H.T., Wheeler, L., Nazlek, J., Kernis, M.H., & Spiegel, N. (1985). On specificity in the impact of social participation on physical and psychological health. Journal of Personality and Social Psychology, 48, 1204–1217.
Rintala, D.H., Young, M.E., Hart, K.A., Clearman, R.R., & Fuhrer, M.J. (1992). Social support and the well-being of persons with spinal cord injury living in the community. Rehabilitation Psychology, 37, 155–163.
Sarason, B.R., Sarason, I.G., & Gurung, R.A.R. (1997). Close personal relationships and health outcomes: A key to the role of social support. In S. Duck (Series Ed.) & B.R. Sarason (Vol. Ed.), Handbook of personal relationships: Theory, research and interventions (2nd ed., pp. 547–573). Chicester: Wiley.
Sarason, I.G., Sarason, B.R., & Pierce, G.R. (1992). Three contexts of social support. In: H. Veiel & U. Baumann (Eds.), The meaning and measurement of social support (pp. 143–154). Washington: Hemisphere.
Schoenbach, V.J., Kaplan, B.H., Fredman, L., & Kleinbaum, D.G. (1986). Socialties and mortality in Evans County, Georgia. American Journal of Epidemiology, 123(4), 577–591.
Schulz, R. & Decker, S. (1985). Long-term adjustment to physical disability: The role of social support, perceived control, and self-blame. Journal of Personality and Social Psychology, 48(5), 1162–1172.
Sherbourne, C.D., Meredith, L.S., Rogers, W., & Ware, J.E. (1992). Social support and stressful life events: Age differences in their effects on health-related quality of life among the chronically ill. Quality of Life Research, 1, 235–246.
Sherwood, N.E. & Jeffrey, R.W. (2000). The behavioral determinants of exercise: Implications for physical activity interventions. Annual Review of Nutrition, 20, 21–44.
Sobsey, D. & Doe, T. (1991). Patterns of sexual abuse and assault. Journal of Sexuality and Disability, 9(3), 243–259.
Thoits, P.A. (1986). Social support as coping assistance. Journal of Consulting and Clinical Psychology, 54, 416–423.
Turner, R.J. & Marino, F. (1994). Social support and social structure: A descriptive epidemiology. Journal of Health and Social Behavior, 35, 193–212.
Unger, D.G. & Wandersman, L.P. (1985). Social support and adolescent mothers: Action research contributions to theory and practice. Journal of Social Issues, 41, 29–45.
US Department of Commerce. (2000). Falling through the net: Toward digital inclusion. A report of American’s access to technology tools [WWW page]. Retrieved July 16, 2003, from http://www.ntia.doc.-gov/ntiahome/fttn00/contents00.html
U.S. Department of Health and Human Services. (2000). Healthy people 2010: Understanding and improving health. objectives for improving health (Part A: Focus areas 1–14), 2nd ed. Washington: U.S. Government Printing Office. Retrieved May 12, 2003, from http://www.healthypeople.gov/Document/tableofcontents.htm#parta
U.S. Department of Transportation, National Highway Traffic Safety Administration (NHTSA). (2009). Traffic Safety Facts 2008: Alcohol-Impaired Driving. Washington (DC): NHTSA. Accessed September 26, 2010 at http://www-nrd.nhtsa.dot.gov/Pubs/811155.PDF
U.S. Department of Health and Human Services. (n.d.). Healthy people with disabilities: HP2010 data on disparities. Retrieved May 12, 2003, from http://www.cdc.gov/ncbddd
Use of Internet is Growing Twice as Fast as Among Rest of Population. (2002). Disability Funding News, 2(4). Silver Spring, MD: CD Publication.
Verbrugge L.M. & Jette, A.M. (1994). The disablement process. Social Science and Medicine, 38(1), 1–14.
Wallhagen, M.I. (1999). Social support in diabetes. Diabetes Spectrum, 12(4), 254–260.
Walster, E., Berscheid, E., & Walster, G.W. (1973). New directions in equity research. Journal of Personality and Social Psychology, 25, 151–176.
Weigel, D., Devereux, P.G., Leigh, G.K., & Ballard-Reisch, D. (1998). A longitudinal study of adolescents’ perceptions of support and stress: Stability and change. Journal of Adolescent Research, 13(2), 158–177.
Westbrook, M.T., Legge, V., & Pennay, M. (1995).Ethnic differences in expectations for women with physical disabilities. Journal of Applied Rehabilitation Counseling, 26(4), 26–33.
White, G.W., Branstetter, A.D., & Seekins, T. (2000). Secondary conditions among people with disabilities from minority cultures; Proceedings and recommendations of a working conference. Lawrence: Research and Training Center on Independent Living; University of Kansas.
Williams, D.R. (2005). Race/ethnicity and socioeconomic status: Measurement and methodological issues. In N. Krieger (Ed.), Embodying inequality: Epidemiologic perspectives, (pp. 158–181). Amityville, NY: Baywood Publishing.
World Health Organization. (2001). International classification of functioning, disability, and health (ICF). Geneva: WHO.
Wortman, C. & Lehman, D. (1985). Reactions to victims of life crisis: Support attempts that fail. In I.G. Sarason & B.R. Sarason (Eds.), Social support: Theory, research, and application (pp. 463–489). Dordrecht, The Netherlands: Martinus Nijhoff.
Wright, B. (1988). Attitudes and the fundamental negative bias: Conditions and corrections. In Yuker, H.E. (Ed.), Attitudes toward persons with disabilities (pp. 3–21). New York: Springer.
Yamaki, K. & Fujiura, G.T. (2002). Employment and income status of adults with developmental disabilities living in the community. Mental Retardation, 40(2), 132–141.
Zola, I. (1993). Disability statistics, what we count and what it tells us: A personal and political analysis. Journal of Disability Policy Studies, 4(2), 10–39.
Bibliography
Brown, D.S. (1994). Working effectively with people with learning disabilities and attention deficit hyperactivity disorder. [Brochure]. Ithaca: Program on Employment and Disability, Cornell University. Available on-line: http://www.ilr.cornell.edu/extension/files/download/Learning_Disability.pdf
Gething, L. (1997). Person to person: A guide for professionals working with people with disabilities. Baltimore: Paul H. Brookes.
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Devereux, P., Bullock, C. (2011). Social and Behavioral Dimensions of Health. In: Lollar, D., Andresen, E. (eds) Public Health Perspectives on Disability. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-7341-2_3
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