JCPSLP Vol 18 no 2 July 2016

References Blyth, C., & Gardner, A. (2007). ‘We’re not asking for anything special’: Direct payments and the carers of disabled children. Disability & society , 22 (3), 235–249. doi: 10.1080/09687590701259427 Caldwell, J., & Heller, T. (2003). Management of respite and personal assistance services in a consumer-directed family support programme. Journal of Intellectual Disability Research , 47 (4–5), 352–367. doi: 10.1046/j.1365- 2788.2003.00496.x CASP. (2014). Critical Appraisal Skills Programme . Retrieved 17 Sept 2014 from http://www.casp-uk.net/ Cowen, A., Murray, P., & Duffy, S. (2011). Personalised transition: A collaborative approach to funding individual budgets for young disabled people with complex needs leaving school. Journal of Integrated Care , 19 (2), 30–36. Crosby, N. (2010). Personalisation: Children, young people and families . Briefing 3: Evaluation and Outcomes. Lancashire, UK: In Control. Crosby, N. (2011). A strategy for change: Making personalisation a reality for children, young people and their families . Lancashire, UK: In Control. Cummins, R. A., Eckersley, R., Pallant, J., van Vugt, J., & Misajon, R. (2003). Development of a national index of subjective wellbeing: The Australian Unity Wellbeing Index. Social Indicators Research , 64 , 159–190. Dew, A., Bulkeley, K., Veitch, C., Bundy, A., Lincoln, M., Brentnall, J., . . . Griffiths, S. (2013). Carer and service providers’ experiences of individual funding models for children with a disability in rural and remote areas. Health & Social Care in the Community , 21 (4), 432–441. doi:http:// dx.doi.org/10.1111/hsc.12032 Donnelly, V., & Brooke-Mawson, I. (2008). Financial freedom. Learning Disability Practice , 11 (10), 27–29. Downs, S. H., & Black, N. (1998). The feasibility of creating a checklist for the assessment of the methodological quality both of randomised and non- randomised studies of health care interventions. Journal of Epidemiology and Community Health , 52 (6), 377–384. doi:10.1136/jech.52.6.377 Glendinning, C., Arksey, H., Jones, K., Moran, N., Netten, A., & Rabiee, P. (2009). The individual budgets pilot projects: Impact and outcomes for carers. York, UK: Social Policy Research Unit, University of York. Glendinning, C., Challis, D., Fernandez, J., Jacobs, S., Jones, K., Knapp, M., . . . Wilberforce, M. (2008). Evaluation of the individual budgets pilot programme: Final report . York, UK: Social Policy Research Unit, University of York. Head, M. J., & Conroy, J. W. (2005). Outcomes of self-determination in Michigan: Quality and costs. In R. J. Stancliffe & K. C. Lakin (Eds.), Costs and outcomes of community services for people with intellectual disabilities (pp. 219–40). Baltimore, MD: Paul H. Brooks Publishing. Heller, T., & Caldwell, J. (2005). Impact of a consumer- directed family support program on reduced out-of-home institutional placement. Journal of Policy and Practice in Intellectual Disabilities , 2 (1), 63-65. doi:10.1111/j.1741- 1130.2005.00010.x

Heller, T., Miller, A. B., & Hsieh, K. (1999). Impact of a consumer-directed family support program on adults with developmental disabilities and their family caregivers. Family Relations , 48 (4), 419–427. Johnson, R., Thom, G., & Prabhakar. (2010). Individual budgets for families with disabled children . Final evaluation report: the family journey. United Kingdom: Department for Education. Mahoney, K. J., Desmond, S. M., Simon-Rusinowitz, L., Loughlin, D. M., & Squillace, M. R. (2002). Consumer preferences for a cash option versus traditional services: Telephone survey results from New Jersey elders and adults. Journal of Disability Policy Studies , 13 (2), 75–87. doi:10.1177/10442073020130020301 Ottmann, G., Laragy, C., & Haddon, M. (2009). Experiences of disability consumer-directed care users in Australia: Results from a longitudinal qualitative study. Health & Social Care in the Community , 17 (5), 466–475. doi:10.1111/j.1365-2524.2009.00851.x Poll, C., & Duffy, S. (2008). A report on In Control’s second phase: Evaluation and learning, 2005–2007 . In Control Publications, London. Prabhakar, M., Thom, G., & Johnson, R. (2010). Individual budgets for families with disabled children: Interim report . United Kingdom: Department for Education. Robinson, S., Gendera, S., Fisher, K. R., Clements, N., Eastman, C., & Oprea, I. (2012). Evaluation of the self directed support pilot for children and young adults with a physical disability: Final report . Sydney, NSW: Social Policy Research Centre, Griffith University. Schwartz, B. (2004). The paradox of choice . New York: Harper Collins Publishers. Weaver, R. (2012). Integrated disability service: Evaluation of Individual Budget Project . Warwickshire, UK: Warwickshire County Council. Welch, V., Hatton, C., Emerson, E., Collins, M., Robertson, J., Langer, S., & Wells, E. (2012). Using direct payments to fund short breaks for families with a disabled child. Child: Care, Health & Development , 38 (6), 900–909. doi:10.1111/j.1365-2214.2011.01339.x West, S. L., King, V., Carey, T. S., Lohr, K. N., McKoy, N., Sutton, S. F., & Lux, L. (2002). Systems to rate the strength of scientific evidence . Washington D.C. USA. Agency for Healthcare Research and Quality, US Department of Health and Human Services. Dr Andrea Simpson is a senior lecturer in Audiology with La Trobe University, Melbourne, Australia. Professor Jacinta Douglas is an internationally recognised researcher in the field of disability following brain injury based at La Trobe University, Melbourne, Australia.

Correspondence to: Dr Andrea Simpson School Allied Health La Trobe University Kingsbury Drive, Bundoora, Victoria, 3086, Australia phone: +61 (03) 9479 1821 email: a.simpson@latrobe.edu.au

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