Abstract
The emotional, financial and social impact on caregivers of those with pediatric psychiatric, emotional and behavioral disorders has been poorly documented. This study sought to begin to remedy this by determining the utility of the Burden Assessment Scale (BAS) with this population. 300 parents seeking services within a major Canadian city were interviewed using the BAS and a follow up questionnaire on the clarity, comprehensiveness and acceptability of the BAS. The BAS was clear, acceptable and comprehensive for >80 % of participants. Factor analysis revealed four factors compared to the original five factors found with adults. The BAS had a utility with this population and would be a valuable addition to standard information gathered but use of the total score only is recommended.
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Notes
Each item on the BAS can be scored 0–3 or 1–4. The reported mean in this study has been adjusted to the 0–3 format to maintain the metric with the original study.
University of Calgary, Faculty of Medicine, Office of Medical Bioethics, Heritage Medical Research Building/Rm 93, 3330 Hospital Drive N.W. Calgary, Alberta, Canada T2N 4N1 Telephone: (403) 220-7990, Fax: (403) 283-8524.
References
Alberta Health and Wellness. (2008). Children’s Mental Health Plan for Alberta. Edmonton. Retrieved from http://www.health.alberta.ca/documents/Mental-Health-Plan-Children-08.pdf.
Bella, G. P., Garcia, M. C., & Spadari-Bratfisch, R. C. (2011). Salivary cortisol, stress, and health in primary caregivers (mothers) of children with cerebral palsy. Psychoneuroendocrinology, 36(6), 834–842. doi:10.1016/j.psyneuen.2010.11.005.
Blader, J. C. (2006). Which family factors predict children’s externalizing behaviors following discharge from psychiatric inpatient treatment? Journal of Child Psychology and Psychiatry and Allied Disciplines, 47(11), 1133–1142. doi:10.1111/j.1469-7610.2006.01651.x.
Braithwaite, V. (1996). Understanding stress in informal caregiving: Is burden a problem of the individual or of society? Research on Aging, 18(2), 139–174. doi:10.1177/0164027596182001.
Caqueo-Urízar, A., & Gutiérrez-Maldonado, J. (2006). Burden of care in families of patients with schizophrenia. Quality of Life Research, 15(4), 719–724. doi:10.1007/s11136-005-4629-2.
Cawthorpe, D., & Wilkes, T. (2007). Priority-setting for children’s mental health: Clinical usefulness and validity of the priority criteria score. Journal of the Canadian Academy of Child Psychiatry, 16(1), 18–26.
Corcoran, K., & Fischer, J. (2000). Measures for clinical practice: A sourcebook volume 1: couples, families and children. New York: The Free Press.
Datta, P., Poortinga, Y. H., & Marcoen, A. (2003). Parent care by Indian and Belgian caregivers in their roles of daughter/daughter-in-law. Journal of Cross-Cultural Psychology, 34(6), 736–749. doi:10.1177/0022022103258589.
Davis, T. S., Gavazzi, S. M., Scheer, S. D., Kwon, I. A., Lammers, A., Fristad, M. A., et al. (2011). Measuring family caregiver perceptions of support in caring for children and youth with mental health concerns. Journal of Social Service Research, 37(5), 500–515. doi:10.1080/01488376.2011.607366.
Deeken, J. F., Taylor, K. L., Mangan, P., Yabroff, K. R., & Ingham, J. M. (2003). Care for the caregivers: A review of self-report instruments developed to measure the burden, needs, and quality of life of informal caregivers. Journal of Pain and Symptom Management, 26(4), 922–953. doi:10.1016/S0885-3924(03)00327-0.
Dimitropoulos, G., Carter, J., Schachter, R., & Woodside, D. B. (2008). Predictors of family functioning in carers of individuals with anorexia nervosa. The International Journal of Eating Disorders, 41(8), 739–747. doi:10.1002/eat.20562.
Friedman-Yakoobian, M. S., Mueser, K. T., Giuliano, A., Goff, D. C., & Seidman, L. J. (2009). Family-directed cognitive adaptation for schizophrenia. Journal of Clinical Psychology, 65(8), 854–867. doi:10.1002/jclp.20611.
Green, S. E. (2004). The impact of stigma on maternal attitudes toward placement of children with disabilities in residential care facilities. Social Science and Medicine, 59(4), 799–812. doi:10.1016/j.socscimed.2003.11.023.
Green, S., Davis, C., Karshmer, E., Marsh, P., & Straight, B. (2005). Living stigma: The impact of labeling, stereotyping, separation, status loss, and discrimination in the lives of individuals with disabilities and their families. Sociological Inquiry, 75(2), 197–215. doi:10.1111/j.1475-682X.2005.00119.x.
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, 47(2), 233–242. doi:10.1007/s10597-010-9298-0.
Gutiérrez-Maldonado, J., Caqueo-Urízar, A., & Kavanagh, D. J. (2005). Burden of care and general health in families of patients with schizophrenia. Social Psychiatry and Psychiatric Epidemiology, 40(11), 899–904. doi:10.1007/s00127-005-0963-5.
Hallam, L. (2007). How involuntary commitment impacts on the burden of care of the family. International Journal of Mental Health Nursing, 16(4), 247–256. doi:10.1111/j.1447-0349.2007.00474.x.
Harvey, K., Burns, T., Fahy, T., Manley, C., & Tattan, T. (2001). Relatives of patients with severe psychotic illness: Factors that influence appraisal of caregiving and psychological distress. Social Psychiatry and Psychiatric Epidemiology, 36(9), 456–461.
Hecht, M. J., Graesel, E., Tigges, S., Hillemacher, T., Winterholler, M., Hilz, M.-J., et al. (2003). Burden of care in amyotrophic lateral sclerosis. Palliative Medicine, 17(4), 327–333. doi:10.1191/0269216303pm754oa.
Hoenig, J., & Hamilton, M. W. (1966). Elderly psychiatric patients and the burden on the household. Psychiatria et Neurologia, 152(5), 281–293.
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. doi:10.2307/2137221.
Ivarsson, A.-B., Sidenvall, B., & Carlsson, M. (2004). The factor structure of the Burden Assessment Scale and the perceived burden of caregivers for individuals with severe mental disorders. Scandinavian Journal of Caring Sciences, 18(4), 396–401. doi:10.1111/j.1471-6712.2004.00298.x.
Kearney, J. A., Britner, P. A., Farrell, A. F., & Robinson, J. L. (2011). Mothers’ resolution of their young children’s psychiatric diagnoses: Associations with child, parent, and relationship characteristics. Child Psychiatry and Human Development, 42(3), 334–348. doi:10.1007/s10578-011-0217-6.
Lipton, H., & Donsky, A. (2012). Healthy minds/healthy children outreach service: Lessons learned after 8 years. Journal of the Canadian Academy of Child and Adolescent Psychiatry/Journal de l’Académie Canadienne de Psychiatrie de L’enfant et de L’adolescent, 21(2), 105–110.
Mackay, C., & Pakenham, K. I. (2012). A stress and coping model of adjustment to caring for an adult with mental illness. Community Mental Health Journal, 48(4), 450–462. doi:10.1007/s10597-011-9435-4.
Mental Health Commission of Canada. (2012). Changing directions: The mental health strategy for Canada. Calgary, AB: Author.
O’Driscoll, C., Heary, C., Hennessy, E., & McKeague, L. (2012). Explicit and implicit stigma towards peers with mental health problems in childhood and adolescence. Journal of Child Psychology and Psychiatry and Allied Disciplines, 53(10), 1054–1062. doi:10.1111/j.1469-7610.2012.02580.x.
Ohaeri, J. U. (2001). Caregiver burden and psychotic patients’ perception of social support in a Nigerian setting. Social Psychiatry and Psychiatric Epidemiology, 36(2), 86–93. doi:10.1007/s001270050294.
Osse, B. H. P., Vernooij-Dassen, M. J. F. J., Schadé, E., & Grol, R. P. T. M. (2007). A practical instrument to explore patients’ needs in palliative care: The problems and needs in palliative care questionnaire short version. Palliative Medicine, 21(5), 391–399. doi:10.1177/0269216307078300.
Rajalin, M., Wickholm-Pethrus, L., Hursti, T., & Jokinen, J. (2009). Dialectical behavior therapy-based skills training for family members of suicide attempters. Archives of Suicide Research, 13(3), 257–263. doi:10.1080/13811110903044401.
Reinhard, S. C., Gubman, G. D., Horwitz, A. V., & Minsky, S. (1994). Burden Assessment Scale for families of the seriously mentally ill. Evaluation and Program Planning, 17(3), 261–269. doi:10.1016/0149-7189(94)90004-3.
Reinhard, S. C., & Horwitz, A. V. (1995). Caregiver burden: Differentiating the content and consequences of family caregiving. Journal of Marriage and the Family, 57(3), 741. doi:10.2307/353928.
Ryan, M. (1994). Caring for people with learning disabilities in Scotland: Comparative costs. British Journal of Learning Disabilities, 22(2), 57–61.
Samele, C., & Manning, N. (2000). Level of caregiver burden among relative of the mentally ill in South Verona. European Psychiatry, 15, 196–204.
Scarnier, M., Schmader, T., & Lickel, B. (2009). Parental shame and guilt: Distinguishing emotional responses to a child’s wrongdoings. Personal Relationships, 16(2), 205–220. doi:10.1111/j.1475-6811.2009.01219.x.
Schmitt-Rodermund, E., & Silbereisen, R. K. (2008). Well-adapted adolescent ethnic German immigrants in spite of adversity: The protective effects of human, social, and financial capital. European Journal of Developmental Psychology, 5(2), 186–209. doi:10.1080/17405620701557290.
Schuntermann, P. (2002). Pervasive developmental disorder and parental adaptation: Previewing and reviewing atypical development with parents in child psychiatric consultation. Harvard Review of Psychiatry, 10(1), 16–27. doi:10.1080/10673220216207.
Seng, B. K., Luo, N., Ng, W. Y., Lim, J., Chionh, H. L., Goh, J., et al. (2010). Validity and reliability of the Zarit Burden Interview in assessing caregiving burden. Annals of the Academy of Medicine, Singapore, 39(10), 758–763.
Shelton, K. H., & Harold, G. T. (2008). Interparental conflict, negative parenting, and children’s adjustment: Bridging links between parents’ depression and children’s psychological distress. Journal of Family Psychology, 22(5), 712–724. doi:10.1037/a0013515.
Skinner, A. C., & Slifkin, R. T. (2007). Rural/urban differences in barriers to and burden of care for children with special health care needs. The Journal of Rural Health, 23(2), 150–157. doi:10.1111/j.1748-0361.2007.00082.x.
Vella, S.-L., & Pai, N. (2013). The measurement of burden of care in serious mental illness: A qualitative review. The Australian and New Zealand Journal of Psychiatry, 47(3), 222–234. doi:10.1177/0004867412468494.
West, A., & Newman, D. (2003). Worried and blue: Mild parental anxiety and depression in relation to the development of young children’s temperament and behavior problems. Parenting: Science and Practice, 3(2), 133–154.
Acknowledgments
This research was supported by a grant from the Alberta Children’s Hospital Foundation. We particularly want to acknowledge tireless and excellent work of the research assistant on this project Natasha Wosnock.
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Murdoch, D.D., Rahman, A., Barsky, V. et al. The Use of the Burden Assessment Scale with Families of a Pediatric Population. Community Ment Health J 50, 703–710 (2014). https://doi.org/10.1007/s10597-014-9724-9
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DOI: https://doi.org/10.1007/s10597-014-9724-9