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Finkelstein, A.; Bachner, Y. G.; Greenberger, C.; Brooks, R.; Tenenbaum, A. – Journal of Intellectual Disability Research, 2018
Background: Although burnout has been recognised as an important stress-related problem among staff working with people with intellectual and developmental disabilities (IDD), literature on the subject is limited yet emerging. The aim of this study is twofold: (1) to evaluate the level of burnout within different professions working with IDD; (2)…
Descriptors: Correlation, Burnout, Intellectual Disability, Developmental Disabilities
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Turk, V.; Kerry, S.; Corney, R.; Rowlands, G.; Khattran, S. – Journal of Intellectual Disability Research, 2010
Background: This research identifies factors affecting why some adults with intellectual disability (AWIDs) consult their general practitioner (GP) more than others. Little is known about these factors, despite AWIDs having higher health needs and reduced longevity. Current barriers to accessing health care need to be understood and overcome to…
Descriptors: Health Needs, Females, Mental Retardation, Access to Health Care
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Hayes, S.; McGuire, B.; O'Neill, M.; Oliver, C.; Morrison, T. – Journal of Intellectual Disability Research, 2011
Background: We investigated the relationship between low mood and challenging behaviour in people in the severe and profound range of intellectual disability, while controlling for the presence of potentially confounding variables such as diagnosis of autism, physical and sensory problems and ill health. Methods: The key workers of 52 people with…
Descriptors: Mental Retardation, Autism, Depression (Psychology), Behavior Problems
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Povee, K.; Roberts, L.; Bourke, J.; Leonard, H. – Journal of Intellectual Disability Research, 2012
Background: This study aimed to explore the factors that predict functioning in families with a child with Down syndrome using a mixed methods design. The quantitative component examined the effect of maladaptive and autism-spectrum behaviours on the functioning of the family while the qualitative component explored the impact of having a child…
Descriptors: Behavior Problems, Foreign Countries, Down Syndrome, Family Relationship
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Chiu, Marcus Y. L.; Hung, Rommel C. H. – Journal of Intellectual Disability Research, 2006
Background: In the light of the existence of lengthy waiting lists for out-of-home placements, this study examines the factors affecting the decision to apply or not to apply for this facility in a city traditionally characterized by a cultural and policy emphasis on family responsibility and by relatively low levels of welfare commitment to…
Descriptors: Foreign Countries, Decision Making, Caregivers, Adults
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Plant, K. M.; Sanders, M. R. – Journal of Intellectual Disability Research, 2007
Background: This study examined the predictors, mediators and moderators of parent stress in families of preschool-aged children with developmental disability. Method: One hundred and five mothers of preschool-aged children with developmental disability completed assessment measures addressing the key variables. Results: Analyses demonstrated that…
Descriptors: Mothers, Developmental Disabilities, Behavior Problems, Predictor Variables
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Keith, K. D.; Bonham, G. S. – Journal of Intellectual Disability Research, 2005
Background: To date researchers have given little attention to the use of quality of life (QOL) data for organization and systems-level change. This article presents two state-level examples of how QOL data are currently used in the USA. Method: Individuals with intellectual disability (ID) were assessed on an ongoing basis using two…
Descriptors: Quality of Life, Mental Retardation, Disabilities, Change Strategies
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Feldman, M.; McDonald, L.; Serbin, L.; Stack, D.; Secco, M. L.; Yu, C. T. – Journal of Intellectual Disability Research, 2007
Background: Despite extensive research with families raising children with or at risk for developmental delay (DD), it is not clear whether primary caregivers of these children are at increased risk for depressive symptoms. Discrepant findings in the literature may be owing to heterogeneity of child problems. More research is needed on child,…
Descriptors: Down Syndrome, Early Intervention, Caregivers, Self Efficacy
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McConkey, R. – Journal of Intellectual Disability Research, 2005
Background: Although the majority of adult persons with intellectual disabilities are cared for by their families, remarkably little is known of the characteristics of their carers, the support services they receive and their unmet needs. A particular concern is whether or not carers have equitable access to services. Method: Information was…
Descriptors: Foreign Countries, Mental Retardation, Adults, Caregivers