Literature DB >> 16513992

Illness representations and lived experience in early-stage dementia.

Guy Harman1, Linda Clare.   

Abstract

The self-regulation model of illness behavior provides a framework for understanding how threats to self from chronic illness can be managed and proposes a significant role for illness representations. This framework can assist in illuminating the experience of developing dementia but has not previously been considered in this context. The authors conducted semistructured interviews with 9 people who had a diagnosis of early-stage dementia to explore illness representations and how these related to daily lived experience, using interpretative phenomenological analysis (IPA). Two over arching themes emerged: It will get worse, reflecting an understanding of dementia; and I want to be me, reflecting a desire to maintain sense of identity. Participants faced a number of personal and interpersonal dilemmas. The authors present a preliminary model of the way in which illness representations contribute to the lived experience of early-stage dementia.

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Year:  2006        PMID: 16513992     DOI: 10.1177/1049732306286851

Source DB:  PubMed          Journal:  Qual Health Res        ISSN: 1049-7323


  28 in total

Review 1.  Health care experiences of people with dementia and their caregivers: a meta-ethnographic analysis of qualitative studies.

Authors:  Jeanette C Prorok; Salinda Horgan; Dallas P Seitz
Journal:  CMAJ       Date:  2013-09-03       Impact factor: 8.262

Review 2.  Using qualitative methods to inform the trade-off between content validity and consistency in utility assessment: the example of type 2 diabetes and Alzheimer's disease.

Authors:  Clare McGrath; Diana Rofail; Elizabeth Gargon; Linda Abetz
Journal:  Health Qual Life Outcomes       Date:  2010-02-12       Impact factor: 3.186

3.  [Subjective perception of and coping with dementia in its early stages. A qualitative interview study with people with dementia and their relatives - SUWADEM].

Authors:  E Stechl; G Lämmler; E Steinhagen-Thiessen; U Flick
Journal:  Z Gerontol Geriatr       Date:  2007-04       Impact factor: 1.281

4.  Predictors of self-reported psychosocial outcomes in individuals with dementia.

Authors:  Nicole T Dawson; Sara M Powers; Maura Krestar; Sarah J Yarry; Katherine S Judge
Journal:  Gerontologist       Date:  2012-10-29

5.  The Experience of Lived Time in People with Dementia: A Systematic Meta-Synthesis.

Authors:  Siren Eriksen; Ruth Louise Bartlett; Ellen Karine Grov; Tanja Louise Ibsen; Elisabeth Wiken Telenius; Anne Marie Mork Rokstad
Journal:  Dement Geriatr Cogn Disord       Date:  2020-11-11       Impact factor: 2.959

6.  Validation of an informant-reported web-based data collection to assess dementia symptoms.

Authors:  Kenneth Rockwood; An Zeng; Chris Leibman; Lisa Mucha; Arnold Mitnitski
Journal:  J Med Internet Res       Date:  2012-03-12       Impact factor: 5.428

7.  What it means to be an adult child of a person with dementia.

Authors:  Annika Kjällman-Alm; Karl-Gustaf Norbergh; Ove Hellzen
Journal:  Int J Qual Stud Health Well-being       Date:  2013-10-22

8.  Creating relationships with persons with moderate to severe dementia.

Authors:  Iréne Ericsson; Sofia Kjellström; Ingrid Hellström
Journal:  Dementia (London)       Date:  2011-10-09

Review 9.  Psychosocial factors that shape patient and carer experiences of dementia diagnosis and treatment: a systematic review of qualitative studies.

Authors:  Frances Bunn; Claire Goodman; Katie Sworn; Greta Rait; Carol Brayne; Louise Robinson; Elaine McNeilly; Steve Iliffe
Journal:  PLoS Med       Date:  2012-10-30       Impact factor: 11.069

10.  Appropriate disclosure of a diagnosis of dementia: identifying the key behaviours of 'best practice'.

Authors:  Jan Lecouturier; Claire Bamford; Julian C Hughes; Jillian J Francis; Robbie Foy; Marie Johnston; Martin P Eccles
Journal:  BMC Health Serv Res       Date:  2008-05-01       Impact factor: 2.655

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