Literature DB >> 15789941

Perspectives on quality of life of people with intellectual disabilities: the interpretation of discrepancies between clients and caregivers.

C G C Janssen1, C Schuengel, J Stolk.   

Abstract

Large discrepancies have sometimes been found between the quality of life (QOL) experienced by clients with intellectual disabilities and their QOL as described by their caregivers. Olsen and Schober (Soc Indi Res 1993; 28: 173-193) may have provided a framework useful to conceptualize such discrepancies. They suggested that lack of concordance between objective circumstances (i.e. poverty) and perceived QOL must not be treated as measurement noise, but as a source of information. They speculated on the psychological processes that underly and explain this lack of concordance; particularly processes that try to deal with the stress induced by cognitive dissonance and learned helplessness. In this study low to moderate agreement was found between caregivers judgement of QOL of individual clients and clients' own perception of QOL. In some areas and for some clients the discrepancies indicated dissonance (caregivers are satisfied, clients are not) and in other areas and for other clients adaptation (clients are satisfied, caregivers are not). There were systematic differences between clients falling in these groups with respect to their personal characteristics and with respect to factual conditions of care. These outcomes are interpreted with respect to Olson and Schober's contentions regarding the psychological processes that underly a person's experience of QOL. The Olson and Schober framework appears to be a fruitful way to combine different sources of information regarding QOL.

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Year:  2005        PMID: 15789941     DOI: 10.1007/s11136-004-1692-z

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   4.147


  13 in total

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Review 2.  Understanding challenging behaviour in people with severe and profound intellectual disability: a stress-attachment model.

Authors:  C G C Janssen; C Schuengel; J Stolk
Journal:  J Intellect Disabil Res       Date:  2002-09

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Authors:  G J Vreeke; C G Janssen; S Resnick; J Stolk
Journal:  Int J Rehabil Res       Date:  1997-09       Impact factor: 1.479

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Journal:  Int J Rehabil Res       Date:  1989       Impact factor: 1.479

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Authors:  C Hatton
Journal:  Ment Retard       Date:  1998-04

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Authors:  D Felce; J Perry
Journal:  Res Dev Disabil       Date:  1995 Jan-Feb

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8.  Quality of life among children aged 2-17 years in the five Nordic countries. Comparison between 1984 and 1996.

Authors:  L T Berntsson; L Köhler
Journal:  Eur J Public Health       Date:  2001-12       Impact factor: 3.367

9.  Measurement of quality of life: current state of the art.

Authors:  J C Flanagan
Journal:  Arch Phys Med Rehabil       Date:  1982-02       Impact factor: 3.966

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Authors:  W M Reynolds; K L Miller
Journal:  Appl Res Ment Retard       Date:  1985
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  4 in total

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Journal:  Community Dent Oral Epidemiol       Date:  2017-01-12       Impact factor: 3.383

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3.  The factors associated with care-related quality of life of adults with intellectual disabilities in England: implications for policy and practice.

Authors:  Stacey Rand; Juliette Malley
Journal:  Health Soc Care Community       Date:  2016-04-24

4.  Is it feasible to assess self-reported quality of life in individuals who are deaf and have intellectual disabilities?

Authors:  Johannes Fellinger; Magdalena Dall; Joachim Gerich; Maria Fellinger; Katharina Schossleitner; William Joseph Barbaresi; Daniel Holzinger
Journal:  Soc Psychiatry Psychiatr Epidemiol       Date:  2020-09-14       Impact factor: 4.328

  4 in total

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