BackgroundLittle progress has been made towards community participation of people with intellectual disability despite it being a policy aim since the 1980s. We aimed to identify the features of programmes designed to support community participation.MethodA scoping review was conducted of peer‐reviewed literature between 2000 and 2015, about interventions to support community participation for adults with intellectual disability.ResultsA small body of evidence relates to the design and effectiveness of interventions to enhance community participation. Seventeen studies reported programmes reflecting three conceptualizations of community participation (as social relationships, as convivial encounter and as belonging) that used strategies such as active mentoring, facilitative support worker practice and arts‐based programmes.ConclusionsStudies showed the diverse and person‐centred nature of community participation and demonstrated the need for larger‐scale studies of promising interventions that include details of costs, and strategies to guide implementation of policies to support community participation.
This paper considers the significance of how staff in residential aged care facilities interpret the non-verbal communication and behaviour of residents vis-a-vis their assessments of residents' preferences and ability to participate in decision-making. It highlights the risks associated with staff members' failure to interpret residents' non-verbal communication and behaviour with reference to residents' backgrounds and prior experiences. It also considers how non-verbal communication implemented by staff may impact residents' emotional state and, as a consequence, decision-making abilities. Drawing on interview data with aged care staff from Queensland and Victoria, it demonstrates that care staff in residential facilities appear to rely heavily on non-verbal signals in assessing the decision-making capacity and preferences of residents with dementia. It also indicates that many staff fail to consider residents' non-verbal communication and behaviour with due consideration of residents' individual histories.
This paper presents the findings of research into Children's Court practice in Victoria (Australia) regarding child protection matters involving parental disability. The research examined Court records of hearings and considered the practices of the Court in the light of the particular needs of parents with a disability. The research found that such parents were often unrepresented and that formal Court interventions only infrequently made recommendations regarding the support, training and advice such parents needed in order to retain or regain care of their children. The anecdotal experience of parents with a disability that their capacity to care was likely to be more harshly judged than that of non-disabled parents, was supported. The research also suggested that the assumption of a nexus between parental disability and inability to care must be challenged, given the imperatives of legislation and child protection philosophy.
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