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Hsiao, C-Y. – Journal of Intellectual Disability Research, 2014
Background: Down syndrome (DS) affects not only children but also their families. Much remains to be learned about factors that influence how families of children with DS function, especially families in non-Western populations. The purpose of this cross-sectional, correlational study was to examine how family demographics, family demands and…
Descriptors: Foreign Countries, Down Syndrome, Family Environment, Social Support Groups
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Miller, E.; Buys, L.; Woodbridge, S. – Journal of Intellectual Disability Research, 2012
Background: Caring for a child with a disability can be a unique and challenging experience, with families often relying on informal networks for support. Often, grandparents are key support resources, yet little is known about their roles and experiences. Reporting on data collected in a larger Australian study, this article explores…
Descriptors: Child Rearing, Family Needs, Quality of Life, Disabilities
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Samuel, P. S.; Hobden, K. L.; LeRoy, B. W.; Lacey, K. K. – Journal of Intellectual Disability Research, 2012
Background: Present day service systems evolved from the traditional model of disability intervention where the child with the disability and the family were viewed as pathological entities that needed to be fixed rather than supported. Scholars have increasingly called for a greater focus on the family in service delivery, but few studies have…
Descriptors: Quality of Life, Disabilities, Family Needs, At Risk Persons
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Hu, X.; Wang, M.; Fei, X. – Journal of Intellectual Disability Research, 2012
Background: The concepts of quality of life and family quality of life (FQOL) are increasingly being studied in the field of intellectual disabilities (ID) in China as important frameworks for: (1) assessing families' need for supports and services; (2) guiding organisational and service delivery system changes; and (3) evaluating quality family…
Descriptors: Delivery Systems, Family Needs, Mental Retardation, Quality of Life
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Ouyang, L.; Grosse, S.; Raspa, M.; Bailey, D. – Journal of Intellectual Disability Research, 2010
Background: The employment impact and financial burden experienced by families of children with fragile X syndrome (FXS) has not been quantified in the USA. Method: Using a national fragile X family survey, we analysed data on 1019 families with at least one child who had a full FXS mutation. Out-of-pocket expenditures related to fragile X were…
Descriptors: Family Needs, Marital Status, Health Insurance, Genetic Disorders
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Thurston, S.; Paul, L.; Loney, P.; Ye, C.; Wong, M.; Browne, G. – Journal of Intellectual Disability Research, 2011
Background: Families supporting children with complex needs are significantly more distressed and economically disadvantaged than families of children without disability and delay. What is not known is the associations and costs of parental psychiatric distress within a multi-diagnosis group of special needs children. Methods: In this…
Descriptors: Family Needs, Economically Disadvantaged, Parenting Styles, Mental Health
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Schwichtenberg, A.; Poehlmann, J. – Journal of Intellectual Disability Research, 2007
Background: Interventions based on applied behaviour analysis (ABA) are commonly recommended for children with an autism spectrum disorder (ASD); however, few studies address how this intervention model impacts families. The intense requirements that ABA programmes place on children and families are often cited as a critique of the programme,…
Descriptors: Intervention, Family Needs, Mothers, Autism