NotesFAQContact Us
Collection
Advanced
Search Tips
Showing 1 to 15 of 33 results Save | Export
Peer reviewed Peer reviewed
Direct linkDirect link
Eskow, Karen; Pineles, Lisa; Summers, Jean Ann – Journal of Policy and Practice in Intellectual Disabilities, 2011
This study examined the effect of services provided through Maryland's Home and Community-Based Services Medicaid waiver for children with autism on several outcomes related to families, specifically family quality of life (FQoL) and employment. The purpose of this study was to assess the impact of the services provided through the Maryland autism…
Descriptors: Autism, Quality of Life, Social Services, Children
Peer reviewed Peer reviewed
Direct linkDirect link
Shooshtari, Shahin; Naghipur, Saba; Zhang, Jin – Journal of Policy and Practice in Intellectual Disabilities, 2012
The authors sought to create a demographic, socioeconomic, and health-related profile of older (40+) Canadian adults with developmental disabilities (DD) residing in their communities, and to enhance current knowledge of their unmet health and social support services needs. They provide a secondary analysis of cross-sectional data from the 2001…
Descriptors: Incidence, Developmental Disabilities, Social Services, Older Adults
Peer reviewed Peer reviewed
Direct linkDirect link
Tossebro, Jan; Bonfils, Inge S.; Teittinen, Antti; Tideman, Magnus; Traustadottir, Rannveig; Vesala, Hannu T. – Journal of Policy and Practice in Intellectual Disabilities, 2012
The authors discuss recent developments in services for people with intellectual disabilities (ID) in the Nordic countries. They note that all of the countries saw important reforms during the 1990s, regarding both deinstitutionalization and decentralization. However, they posit that the litmus test of the reforms is not what happens during reform…
Descriptors: Municipalities, Political Science, Mental Retardation, Normalization (Disabilities)
Peer reviewed Peer reviewed
Direct linkDirect link
Jecker-Parvex, Maurice; Breitenbach, Nancy – Journal of Policy and Practice in Intellectual Disabilities, 2012
Despite a long-standing tradition of institutional placement in Switzerland, many older adults with intellectual disabilities continue to be supported by aging parents and siblings. For various reasons, these carers and the adults concerned have been overlooked up to now. To find out how many such families are providing housing and care of this…
Descriptors: Foreign Countries, Caregivers, Older Adults, Mental Retardation
Peer reviewed Peer reviewed
Direct linkDirect link
Cohen, Shana R. – Journal of Policy and Practice in Intellectual Disabilities, 2013
Community services and supports for children with intellectual disabilities (ID) can ameliorate the negative effects of caregiving and enhance child outcomes. For example, in Central and South America, many children with disabilities are institutionalized with inadequate sanitation and medical care. In the United States, certain demographic…
Descriptors: Advocacy, Foreign Countries, Medical Services, Caregivers
Peer reviewed Peer reviewed
Direct linkDirect link
Suemitsu, Shigeru – Journal of Policy and Practice in Intellectual Disabilities, 2009
The author outlines the history, current situation, and the future of the care and support system for people with intellectual and multiple disabilities in Japan. He describes how the service system has been shaped from within by Japanese legislation dating back to the Child Welfare Act of 1947, and how international events such as the…
Descriptors: Multiple Disabilities, Well Being, Foreign Countries, Mental Retardation
Peer reviewed Peer reviewed
Direct linkDirect link
Schippers, Alice; van Boheemen, Marleen – Journal of Policy and Practice in Intellectual Disabilities, 2009
Professional services for persons with intellectual disabilities (ID) have begun to attach more importance to their environment. The concept of (family-related) quality of life proved to link very well with this idea and lent itself to constructing and evaluating services. One outcome was the emergence of equal partnerships between families,…
Descriptors: Mental Retardation, Quality of Life, Young Adults, Professional Services
Peer reviewed Peer reviewed
Direct linkDirect link
McConnell, David; Matthews, Jan; Llewellyn, Gwynnyth; Mildon, Robyn; Hindmarsh, Gabrielle – Journal of Policy and Practice in Intellectual Disabilities, 2008
Parents with intellectual disabilities, like all other parents, need support with child rearing. Often this support comes from family and friends, but in the case of parents with intellectual disabilities, they are more likely to have to rely on the service system. Research from a number of countries demonstrates that there is limited system…
Descriptors: Community Programs, Mental Retardation, Parent Education, Child Rearing
Peer reviewed Peer reviewed
Direct linkDirect link
Hamlin, Alexandra; Oakes, Peter – Journal of Policy and Practice in Intellectual Disabilities, 2008
Deinstitutionalization has been the hallmark of public policy for people with intellectual disabilities within many countries in the developed world for the past 40 years. Although within Britain deinstitutionalization is set to be completed by the end of 2008, beyond the simple closure of hospitals, the success of this initiative can at best be…
Descriptors: Mental Retardation, Hospitals, Normalization (Disabilities), Foreign Countries
Peer reviewed Peer reviewed
Direct linkDirect link
Miller, Emma; Cooper, Sally-Ann; Cook, Ailsa; Petch, Alison – Journal of Policy and Practice in Intellectual Disabilities, 2008
An emphasis on the outcomes of health and social care services has become increasingly apparent within public policy in the United Kingdom. Alongside this, working in partnership has been a key theme, despite a relatively underdeveloped evidence base. Of central importance, however, must be whether directives toward partnership working are…
Descriptors: Mental Retardation, Quality of Life, Foreign Countries, Public Policy
Peer reviewed Peer reviewed
Direct linkDirect link
Sen, Reena; Goldbart, Juliet; Kaul, Sudha – Journal of Policy and Practice in Intellectual Disabilities, 2008
The Indian Institute for Cerebral Palsy (IICP) has been providing education and other services in Kolkata, Eastern India, for children and young adults with cerebral palsy and related disabilities for over 30 years. IICP started by providing education for just two children, and was highly dependent on western expertise. Described is the history of…
Descriptors: Multiple Disabilities, Cerebral Palsy, Young Adults, Nongovernmental Organizations
Peer reviewed Peer reviewed
Direct linkDirect link
Maes, Bea; Van Puyenbroeck, Joris – Journal of Policy and Practice in Intellectual Disabilities, 2008
The authors attempted to find out to what extent and in which ways, in Belgium, have Flemish services for people with intellectual disability adapted to the specific needs of aging people. A study was undertaken and a questionnaire was developed to address the following research topics: (1) accommodations and personnel, (2) staff working methods,…
Descriptors: Mental Retardation, Personnel Management, Down Syndrome, Measures (Individuals)
Peer reviewed Peer reviewed
Direct linkDirect link
Reynolds, Sile; Guerin, Suzanne; McEvoy, John; Dodd, Philip – Journal of Policy and Practice in Intellectual Disabilities, 2008
The impact of a staff-training program on knowledge and confidence in supporting people with intellectual disabilities (ID) at the time of bereavement was examined. Thirty-three staff members from a Dublin, Ireland-based ID support service participated in the study. Both the training (n = 17) and control (n = 16) groups completed measures of…
Descriptors: Well Being, Social Services, Social Support Groups, Grief
Peer reviewed Peer reviewed
Direct linkDirect link
Tarleton, Beth; Ward, Linda – Journal of Policy and Practice in Intellectual Disabilities, 2007
The international literature on parents with intellectual disabilities (ID) has focused on concerns about their ability to parent and strategies to enable them to develop parenting skills. Traditionally, the views and experiences of parents themselves have not been the focus of studies. With this in mind, the authors talked to a cohort of 30…
Descriptors: Mental Retardation, Family Life, Child Rearing, Parents
Peer reviewed Peer reviewed
Direct linkDirect link
Martin, Lynn; Hirdes, John P.; Fries, Brant E.; Smith, Trevor F. – Journal of Policy and Practice in Intellectual Disabilities, 2007
This paper describes the development of the interRAI-Intellectual Disability (interRAI ID), a comprehensive instrument that assesses all key domains of interest to service providers relative to a person with an intellectual disability (ID). The authors report on the reliability and validity of embedded scales for cognition, self-care, aggression,…
Descriptors: Mental Retardation, Dementia, Psychometrics, Depression (Psychology)
Previous Page | Next Page ยป
Pages: 1  |  2  |  3