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Original Article

Decision-making by community residents with an intellectual disability

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Pages 1-8 | Published online: 10 Jul 2009

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Read on this site (7)

Marco O. Bertelli, Annamaria Bianco, Andrea Rossi, Michele Mancini, Giampaolo La Malfa & Ivan Brown. (2019) Impact of severe intellectual disability on proxy instrumental assessment of quality of life. Journal of Intellectual & Developmental Disability 44:3, pages 272-281.
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W.M.L. Finlay, C. Walton & C. Antaki. (2008) Promoting choice and control in residential services for people with learning disabilities. Disability & Society 23:4, pages 349-360.
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Annemaree Carroll, Deb Keen, Clinton Davies, Terry Skehan & Eva Fritz. (2005) Knowledge and understanding of choice diversity of residential care staff working with individuals with intellectual disabilities. The Australian Educational and Developmental Psychologist 22:2, pages 84-97.
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Adrian F. Ashman & Janene Suttie. (1995) Changing existing services for older people with an intellectual disability. Australia and New Zealand Journal of Developmental Disabilities 20:3, pages 189-204.
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Jo Jenkinson & Robyn Nelms. (1994) Patterns of decision-making behaviour by people with intellectual disability: An exploratory study. Australia and New Zealand Journal of Developmental Disabilities 19:2, pages 99-109.
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Articles from other publishers (20)

Anastasia Hronis, Lynette Roberts & Ian I. Kneebone. (2017) A review of cognitive impairments in children with intellectual disabilities: Implications for cognitive behaviour therapy. British Journal of Clinical Psychology 56:2, pages 189-207.
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Joanne Watson. (2016) Assumptions of Decision-Making Capacity: The Role Supporter Attitudes Play in the Realisation of Article 12 for People with Severe or Profound Intellectual Disability. Laws 5:1, pages 6.
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Anika Bexkens, Brenda R. J. Jansen, Maurits W. Van der Molen & Hilde M. Huizenga. (2015) Cool Decision-Making in Adolescents with Behavior Disorder and/or Mild-to-Borderline Intellectual Disability. Journal of Abnormal Child Psychology 44:2, pages 357-367.
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Charles Antaki, W. M. L. Finlay, Chris Walton & Joe Sempik. 2016. The Palgrave Handbook of Adult Mental Health. The Palgrave Handbook of Adult Mental Health 613 632 .
E. Reuzel, P. J. C. M. Embregts, A. M. T. Bosman, M. van Nieuwenhuijzen & A. Jahoda. (2012) Interactional patterns between staff and clients with borderline to mild intellectual disabilities. Journal of Intellectual Disability Research 57:1, pages 53-66.
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Claudia Claes, Stijn Vandevelde, Geert Van Hove, Jos van Loon, Griet Verschelden & Robert Schalock. (2012) Relationship between Self‐Report and Proxy Ratings on Assessed Personal Quality of Life‐Related Outcomes. Journal of Policy and Practice in Intellectual Disabilities 9:3, pages 159-165.
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Wendy Mitchell. (2012) Parents' accounts: Factors considered when deciding how far to involve their son/daughter with learning disabilities in choice-making. Children and Youth Services Review 34:8, pages 1560-1569.
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Emily Shea Tanis, Susan Palmer, Michael Wehmeyer, Daniel K Davies, Steven E Stock, Kathy Lobb & Barbara Bishop. (2012) Self-Report Computer-Based Survey of Technology Use by People With Intellectual and Developmental Disabilities. Intellectual and Developmental Disabilities 50:1, pages 53-68.
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I. Khemka, L. Hickson, M. Casella, N. Accetturi & M. E. Rooney. (2009) Impact of coercive tactics on the decision-making of adolescents with intellectual disabilities. Journal of Intellectual Disability Research 53:4, pages 353-362.
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W. M. L. Finlay, Charles Antaki & Chris Walton. (2008) Saying no to the staff: an analysis of refusals in a home for people with severe communication difficulties. Sociology of Health & Illness 30:1, pages 55-75.
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Charles Antaki, W.M.L. Finlay & Chris Walton. (2016) Conversational Shaping: Staff Members' Solicitation of Talk From People With an Intellectual Impairment. Qualitative Health Research 17:10, pages 1403-1414.
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Charles AntakiChris WaltonW.M.L. Finlay. (2016) How proposing an activity to a person with an intellectual disability can imply a limited identity. Discourse & Society 18:4, pages 393-410.
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L. Nota, S. Soresi & J. Perry. (2006) Quality of life in adults with an intellectual disability: the Evaluation of Quality of Life Instrument. Journal of Intellectual Disability Research 50:5, pages 371-385.
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Robert A. Cummins. (2005) Caregivers as Managers of Subjective Wellbeing: A Homeostatic Perspective. Journal of Applied Research in Intellectual Disabilities 18:4, pages 335-344.
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Linda Dye, Dougal Hare & Steve Hendy. (2003) Factors Impacting on the Capacity to Consent in People with Learning Disabilities. Tizard Learning Disability Review 8:3, pages 11-20.
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Jonathan Perry & David Felce. (2002) Subjective and Objective Quality of Life Assessment: Responsiveness, Response Bias, and Resident:Proxy Concordance. Mental Retardation 40:6, pages 445-456.
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Robert A. Cummins. 2002. 183 207 .
Roger J Stancliffe. (2000) Proxy respondents and quality of life. Evaluation and Program Planning 23:1, pages 89-93.
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R. J. Stancliffe. (2001) Proxy respondents and the reliability of the Quality of Life Questionnaire Empowerment factor. Journal of Intellectual Disability Research 43:3, pages 185-193.
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Kirsten Stalker & Philip Harris. (2010) The Exercise of Choice by Adults with Intellectual Disabilities: A Literature Review. Journal of Applied Research in Intellectual Disabilities 11:1, pages 60-76.
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