Abstract
This study examined the predictors of depressive symptomatology among caregivers of persons with chronic mental illness. Data were collected through in-person interviews with family caregivers of 103 adults with chronic mental illness who were served by mental health case management agencies. The results indicated that insufficiency of overall social support was the most powerful predictor of caregiver depressive symptomatology. In addition, caregiver burden had a significant unique contribution to caregiver depressive symptomatology, with higher levels of burden associated with greater levels of caregiver depressive symptomatology. Higher levels of client behavioral problems and insufficient support from family members and mental health professionals related to the caregiving role were associated with higher levels of caregiver depressive symptomatology through their associations with care-giver burden. Caregiver race was not significantly related to caregiver burden or to caregiver depressive symptomatology after controlling for other variables. Over two-fifths of White caregivers and over one-quarter of Black caregivers were at risk for clinical depression. Implications for practice and research are discussed.
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REFERENCES
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
Biegel, D.E., Sales, E., & Schulz, R. (1991). Family Caregiving in Chronic Illness. Newbury Park: Sage Publications.
Biegel, D.E., Song, L., & Chakravarthy, V. (1994). Predictors of caregiver burden among support group members of persons with chronic mental illness. In E. Kahana, D. E. Biegel & M. L. Wykle (Eds.), Family Caregiving across the Lifespan. Thousand Oaks, CA: Sage Publications, Inc.
Biegel, D.E., Song, L., & Milligan, S. (1995). A comparative analysis of family caregivers perceived relationships with mental health professionals: A comparative analysis. Psychiatric Services, 1995, 46(5), 477-482.
Biegel, D E., & Tracy, E. (1993). Natural Supports Project. Final Report to the Ohio Department of Mental Health. Cleveland: Case Western Reserve University.
Cohen, D., & Eisdorfer, C. (1988). Depression in family members caring for a relative with Alzheimer's disease. Journal of the American Geriatrics Society, 36, 885-889.
Cohen, S., Mermelstein, R., Kamarck, T., & Hoberman, H. (1985). Measuring the functional components of social support. In I.G. Sarason & B.R. Sarason (Eds.), Social Support: Theory, Research and Applications (pp.73-94). The Hague, Netherlands: Martinus Nijhoff.
Corcoran, K., & Fischer, J. (1987). Measures for Clinical Practice—A Sourcebook. New York: The Free Press.
Cox, C., & Monk, A. (1990). Minority caregivers of dementia victims: A comparison of black and hispanic families. The Journal of Applied Gerontology, 9(3), 340-354.
Cutler, D. L., & Tatum, E. (1983). Networks and the chronic patient. In D.L. Cutler (Ed.), Effective Aftercare for the 1980s. New directions for mental health services, No. 19 (pp. 13-22). San Francisco: Jossey-Bass.
Davis, A., Dinitz, S., & Pasaminick, B. (1974). Schizophrenics in the new custodial community. Columbus: Ohio State University Press.
Doll, W. (1976). Family coping with the mentally ill: An unanticipated problem of deinstitutionalization. Hospital and Community Psychiatry, 27(3), 183-185.
Fisher, G. A., Benson, P. R., & Tessler, R. C. (1990). Family response to mental illness. Research in Community and Mental Health, 6, 203-236.
Gallagher, D., Rose, J., Rivera, P., Lovett, S., & Thompson, L. W. (1989). Prevalence of depression in family caregivers. The Gerontologist, 29(4), 449-456.
Grad, J. P. D., & Sainsbury, P. M. D. (1963). Mental illness and the family. Lancet, 1, 544-547.
Greene, V. L., & Monahan, D. J. (1989). The effect of a support and education program on stress and burden among family caregivers to frail elderly persons. The Gerontologist, 29(4), 472-477.
Grella, C. E., & Grusky, O. (1989). Families of the seriously mentally ill and their satisfaction with services. Hospital and Community Psychiatry, 40, 831-835.
Haley, W.E., Levine, E.G., Brown, S.L., & Bartolucci, A. A. (1987). Stress, appraisal, coping, and social support as predictors of adaptational outcome among dementia caregivers. Psychology and Aging, 2(4), 323-330.
Haley, W.E., Levine, E.G., Brown, S.L., Berry, J.W., & Hughes, G.W. (1987). Psychological, social, and health consequences of caring for a relative with senile dementia. Journal of the American Geriatric Society, 35, 405-411.
Hanson, J. (1991). The family perspective of the early stages of severe mental illness. Families in Society.
Hatfield, A. B. (1978). Psychological costs of schizophrenia to the family. Social Work, 355-359.
Holden, D. F., & Lewine, R. R. J. (1982). How families evaluate mental health professionals, resources and effects of illness. Schizophrenia Bulletin, 8, 626-633.
Hollingshead, A. B. & Redlich, F. C. (1958). Social Class and Mental Illness. New York: Wiley and Son.
House, J. (1974). Occupational stress and coronary heart disease: A review and theoretical integration. Journal of Health and Social Behavior, 15, 12-27.
Jackson, J. J. (1991). Life in Black America. Newbury Park, CA: Sage Publications.
Jones, D. A., & Peters, T. J. (1992). Caring for elderly dependents: Effects on the carers' quality of life. Age and Aging, 21, 421-428.
Kahan, J., Kemp, B., Staples, F. R., & Brummel-Smith, K. (1985). Decreasing the burden in families caring for a relative with a dementing illness: A controlled study. Journal of the American Geriatrics Society, 33(10), 664-670.
Kreisman, D., & Joy, V. D. (1974). Family response to the mental illness of a relative: A review of the literature. Schizophrenia Bulletin, 10, 34-57.
Lefley, H. P. (1989). Family burden and family stigma in major mental illness. American Psychologist, 44(3), 556-560.
McFarlane, W. R. (1993). Psychoeducational multi-family groups: Are they a treatment of choice for schizophrenia? Presented in the Annual Forum held by Center for Practice Innovations, Mandel School of Applied Social Sciences, Case Western Reserve University, Cleveland, Ohio
Morrissey, E., Becker, J., & Rubert, M. P. (1990). Coping resources and depression in the caregiving spouses of Alzheimer patients. British Journal of Medical Psychology, 63, 161-171.
Oldridge, M.L. & Hughes, I.C.T. (1992). Psychological well-being in families with a member suffering from Schizophrenia: An investigation into long-standing problems. British Journal of Psychiatry, 16, 249-251.
Pasaminick, B., Scarpetti, F., & Dinitz, S. (1967). Schizophrenics in the Community: An Experimental Study in the Prevention of Rehospitalization. New York: Appleton-Century-Crofts.
Pickett, S. A., Vraniak, D. A., Cook, J. A., & Cohler, B. J. (1993). Strength in adversity: Blacks bear burden better than whites. Professional Psychology: Research and Practice, 24(4), 460-467.
Pruchno, R. A., & Resch, N. L. (1989). Husbands and wives as caregivers: Antecedents of depression and burden. The Gerontologist, 29(2), 159-165.
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.
Rivera, P. A., Rose, J. M., Futterman, A., Lovett, S. B., & Gallagher-Thompson, D. (1991). Dimensions of perceived social support in clinically depressed and non-depressed female caregivers. Psychology and Aging, 6(2), 232-237.
Schulz, R. (1990). Theoretical perspectives on caregiving: Concepts, variables and methods. In D.E. Biegel & A. Blum (Eds.), Aging and Caregiving: Theory, Research & Policy, pp. 27-52. Newbury Park, CA: Sage Publications.
Schulz, R., & Williamson, G. M. (1991). A 2-year longitudinal study of depression among Alzheimer's caregivers. Psychology and Aging, 6(4), 569-578.
Struening, E.L., Stueve, A., Vine, P., Kreisman, D.E., Link, B.G., & Herman, D.B. (1995). Factors associated with grief and depressive symptoms in caregivers of people with serious mental illness. Research in Community and Mental Health, 8, 91-124.
Thompson, S. C., Bundek, N., & Sobolew-Schubin, A. (1990). The caregivers of stroke patients: An investigation of factors associated with depression. Journal of Applied Social Psychology, 20(2), 115-129.
Townsend, A., Noelker, L., Deimling, G., & Bass, D. (1989). Longitudinal impact of inter-household caregiving on adult children's mental health. Psychology and Aging, 4(4)393-401.
Zarit, S. H., Reever, K. E., & Bach-Peterson, J. (1980). Relatives of impaired elderly: Correlates of feelings of burden. The Gerontologist, 20, 649-655.
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Song, LY., Biegel, D.E. & Milligan, S.E. Predictors of Depressive Symptomatology Among Lower Social Class Caregivers of Persons with Chronic Mental Illness. Community Ment Health J 33, 269–286 (1997). https://doi.org/10.1023/A:1025090906696
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DOI: https://doi.org/10.1023/A:1025090906696