Socio-Demographic Predictors of Perceived Burden of Care among Care Givers of Non-Mentally and Mentally Retarded Students in Ibadan, Nigeria

Olaseni Abayomi Oladele; Okhakhume Aide Sylvester

doi:10.46281/aesr.v5i2.362

Olaseni Abayomi Oladele Department of Pure and Applied Psychology, Adekunle Ajasin University, Akungba, Nigeria
Okhakhume Aide Sylvester Department of Psychology, University of Ibadan, Ibadan, Nigeria

DOI: https://doi.org/10.46281/aesr.v5i2.362

Keywords: Demographic factors, Social support, Burden of care, Mentally retarded

Abstract

The care of mentally retarded children is often stressful experiences for family members, as the child grows up and disability becomes quite noticeable by others, parents face a very distressing predicament of social embarrassment and stigma, they require more attention and time while at the same time the need for special equipment, and medical care increases; implicating financial income and capability of the care providers. The aftermath effect on the care provider(s) most often is restrictive and disruptive to economic, social or emotional deficiency. The study examines the influence of socio-demographic variables on care burden of care providers of non-mentally and mentally retarded students in Ibadan metropolis. The study adopted cross sectional research design across types of job, social support, religion, ethnicity and age. A total number of 100 care providers participated in the study (50 care providers of non-mentally retarded students & 50 care providers of the mentally retarded students). The instruments that were used was Care Givers Burden Scale developed by Zarit et al (1980). The result of the study revealed that demographic variables (age, sex, marital status, education level, job type, religion and ethnicity) do not jointly predict burden of care among care providers of mentally retarded students in Ibadan metropolis. [F(7,43)=1.722;p>.05], but revealed that demographic variables jointly predict burden of care among care providers of non-mentally retarded students in Ibadan metropolis. [F(7,43)=2.39;p<.05], and finally revealed that social support had significant influence on burden of care among care providers of mentally retarded students in Ibadan metropolis [t(98)= 11.13; P<.05]. The study therefore concludes that demographic variables jointly predict burden of care among care providers of non-mentally retarded students not mentally retarded students. While social support was found to significantly influence burden of care among care providers of mentally retarded students in Ibadan metropolis.

References

Beckman, P. (1991). Comparison of mothers' and fathers' perceptions of the effect of young children with and without disabilities. American Journal on Mental Retardation, 95, 585-595.

Byrne, E., & Cunningham, C. (1985). The effects of mentally handicapped children on families-a conceptual review. Journal of Child Psychology and Psychiatry, 26, 847-864.

Caqueo-Urízar & J. Gutiérrez-Maldonado. (2006). Burden of care in families of patients with schizophrenia,Quality of Life Research, 15(4),719–724

Corey M. Clark. (2005) “Relation between Social support and physical health”. - Rochester Institute of Technology.

Featherstone, H. (1980). A difference in the family: living with disabled child. New York, Basic Books.

Friedrich, W., & Friedrich, N. (1981). Psychological assets of parents of handicapped and nonhandicapped children. American Journal of Mental Deficiency, 85, 551-553.

Heykyung oh, et,al, (2009) care giver burden and social support among mother rising children with developmental disability in South Korea. International Journal of disability, Development and Education, 56, 149-167.

Kazak, A.E., & Wilcox, B.L. (1984). The structure and function of social support networks in families with handicapped children. American Journal of Community Psychology, 12, 645-661.

Mary E Hayden and Tamar Heller (1997) Support, Problem-Solving/Coping Ability, and Personal Burden of Younger and Older Caregivers of Adults with Mental Retardation. Mental Retardation,35(5),364-372.

Mc Andrew, I. (1976). Children with a handicap and their families. Child: Care, Health and Development, 2, 213-237.

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.

Turnbull, A., Summers, J., & Brotherson, M. (1986). Family life cycle: Theoretical and empirical implications and future directions for families with mentally retarded members. In J. J. Gallagher & P. M. Vietze (Eds.), Families of handicapped persons: Research,programs, and policy issues. Baltimore: Paul H. Brookes.

Wikler L, Wason M and Halfied E. (1981) .Chronic Sorrow revisited. Parent vs Professional Deception of the adjustment of parents of mentally retarded children, Americian Journal of orthopsychiatry, 51-63.

Zahid M.A., & J. U. (2010) .Ohaeri.Relationship of family caregiver burden with quality of care and psychopathology in a sample of Arab subjects with schizophrenia, BMC Psychiatry,10(71).