Literature DB >> 12461762

When a little knowledge is a dangerous thing...: a study of carers' knowledge about dementia, preferred coping style and psychological distress.

Rebekah Proctor1, Carol Martin, Jenny Hewison.   

Abstract

OBJECTIVES: The aim of this study was to improve understanding of the relationship between carers' existing knowledge about dementia, their coping style and psychological morbidity.
METHOD: Fifty carers and patients attending day services were recruited. Carers were given questionnaires to assess knowledge of dementia, preferred coping style, anxiety, depression and strain.
RESULTS: The results indicated that carers who demonstrated more knowledge about the biomedical aspects of dementia were more anxious (p < 0.05). Furthermore, carers who had a preferred coping style of monitoring for threat relevant information were more anxious (p < 0.005).
CONCLUSIONS: Understanding more about those factors that are associated with knowledge about dementia will help to identify profiles of carers who are in need of education and in matching individually tailored interventions to carers with specific learning needs. Copyright 2002 John Wiley & Sons, Ltd.

Entities:  

Mesh:

Year:  2002        PMID: 12461762     DOI: 10.1002/gps.762

Source DB:  PubMed          Journal:  Int J Geriatr Psychiatry        ISSN: 0885-6230            Impact factor:   3.485


  8 in total

1.  Demographic and contextual factors related to knowledge about Alzheimer's disease.

Authors:  Brian D Carpenter; Sarah M Zoller; Steve Balsis; Poorni G Otilingam; Margaret Gatz
Journal:  Am J Alzheimers Dis Other Demen       Date:  2011-01-13       Impact factor: 2.035

2.  A qualitative study of professional and client perspectives on information flows and decision aid use.

Authors:  Christine Stirling; Barbara Lloyd; Jenn Scott; Jenny Abbey; Toby Croft; Andrew Robinson
Journal:  BMC Med Inform Decis Mak       Date:  2012-03-29       Impact factor: 2.796

3.  The Alzheimer's Disease Knowledge Scale: development and psychometric properties.

Authors:  Brian D Carpenter; Steve Balsis; Poorni G Otilingam; Priya K Hanson; Margaret Gatz
Journal:  Gerontologist       Date:  2009-03-25

4.  Ethnic differences in beliefs regarding Alzheimer disease among dementia family caregivers.

Authors:  Heather L Gray; Daniel E Jimenez; Michael A Cucciare; Hui-Qi Tong; Dolores Gallagher-Thompson
Journal:  Am J Geriatr Psychiatry       Date:  2009-11       Impact factor: 4.105

5.  Family carers' experiences of attending a multicomponent psychosocial intervention program for carers and persons with dementia.

Authors:  Aud Johannessen; Frøydis Kristine Bruvik; Solveig Hauge
Journal:  J Multidiscip Healthc       Date:  2015-02-12

6.  Enhancing resourcefulness to improve outcomes in family caregivers and persons with Alzheimer's disease: a pilot randomized trial.

Authors:  Elizabeth W Gonzalez; Marcia Polansky; Carol F Lippa; Laura N Gitlin; Jaclene A Zauszniewski
Journal:  Int J Alzheimers Dis       Date:  2014-09-29

7.  Self-reported symptoms of depression and anxiety among informal caregivers of persons with dementia: a cross-sectional comparative study between Sweden and Italy.

Authors:  Joseba Wulff; Agneta Malmgren Fänge; Connie Lethin; Carlos Chiatti
Journal:  BMC Health Serv Res       Date:  2020-12-02       Impact factor: 2.655

8.  Dementia knowledge assessment scale (DKAS): confirmatory factor analysis and comparative subscale scores among an international cohort.

Authors:  Michael J Annear; Chris Toye; Kate-Ellen J Elliott; Frances McInerney; Claire Eccleston; Andrew Robinson
Journal:  BMC Geriatr       Date:  2017-07-31       Impact factor: 3.921

  8 in total

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