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dc.contributor.authorAndrews, J.
dc.contributor.authorLeonard, H.
dc.contributor.authorHammond, G.
dc.contributor.authorGirdler, Sonya
dc.contributor.authorRajapaksa, R.
dc.contributor.authorBathgate, Katherine
dc.contributor.authorDowns, J.
dc.date.accessioned2017-01-30T13:15:30Z
dc.date.available2017-01-30T13:15:30Z
dc.date.created2013-10-07T20:00:30Z
dc.date.issued2013
dc.identifier.citationAndrews, Jaimi and Leonard, Helen and Hammond, Geoffrey C. and Girdler, Sonya and Rajapaksa, Ruwani and Bathgate, Katherine and Downs, Jenny. 2014. Community Participation for Girls and Women Living with Rett Syndrome. Disability and Rehabilitation. 36 (11): pp. 894-899.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/29826
dc.identifier.doi10.3109/09638288.2013.813083
dc.description.abstract

OBJECTIVE: To describe the relationships between impairment and contextual factors and community participation for girls and women with Rett syndrome.METHODS: Data was collected from a questionnaire completed in 2009 by families participating in the Australian Rett Syndrome Database (n=214). Univariate and multivariate logistic regression were used to analyse relationships between impairment, personal and environmental factors and community participation.RESULTS: The mean age of the girls and women was 17.6 years (SD=7.95, range 3 to 34 years) with 114 (53.3%) girls still at school and 100 (46.7%) women post school. Frequency of activities was influenced by level of walking, community support and maternal education. For girls living at home, participation in activities was associated with greater functional independence and higher levels of maternal education. Participation in recreational (90.1%), physical/skill-based (67.6%) and/or social (70.3%) activities was commonly reported by families, while self-improvement (17.6%) activities were less reported. Younger girls participated in activities mainly with family members and older girls more frequently participated with carers.CONCLUSION: Participation for girls and women with Rett syndrome could be enhanced by stronger local community supports. There are also needs for the implementation of policies that ensure resources are available and accessible by those communities most in need.

dc.publisherInforma Healthcare
dc.subjectInternational Classification of Functioning
dc.subjectRett syndrome
dc.subjectdisability and health
dc.subjectdisability
dc.subjectCommunity participation
dc.titleCommunity Participation for Girls and Women Living with Rett Syndrome
dc.typeJournal Article
dcterms.source.startPage1
dcterms.source.endPage6
dcterms.source.issn0963-8288
dcterms.source.titleDisability and Rehabilitation
curtin.department
curtin.accessStatusFulltext not available


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