Literature DB >> 2737174

Further explorations of common-sense representations of common illnesses.

R R Lau1, T M Bernard, K A Hartman.   

Abstract

A simple method is presented for measuring people's illness cognitions--their common-sense representations of common illnesses. Data were collected from 1,628 different respondents who described a recent illness form 1 to 3 separate times over a 17-month period. A free-clustering task performed by a set of naive participants confirmed that these cognitions fall into the five components that have been previously noted: identity, time line, consequences, cause, and cure. These five components are found to be reasonably stable over time and across different illness episodes. Several consequences of these illness cognitions, in terms of changes in health-locus-of-control beliefs and different propensities to visit a doctor, are also noted. Specifically, controllable attributions for getting sick and personal responsibility attributions for getting better are associated with increased beliefs in Self-Control Over Health and decreased beliefs in Chance Health Outcomes; people with strong Identity and Cure components in their common-sense representations of common illnesses have a greater propensity to visit a doctor when feeling ill.

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Mesh:

Year:  1989        PMID: 2737174     DOI: 10.1037//0278-6133.8.2.195

Source DB:  PubMed          Journal:  Health Psychol        ISSN: 0278-6133            Impact factor:   4.267


  38 in total

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3.  An update on the representational approach to patient education.

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4.  A randomized trial of a representational intervention for cancer pain: does targeting the dyad make a difference?

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Journal:  Health Psychol       Date:  2009-09       Impact factor: 4.267

5.  The Medication Attribution Scale: perceived effects of antiretrovirals and quality of life.

Authors:  S Aversa; C Kimberlin; R Segal
Journal:  Qual Life Res       Date:  1998-04       Impact factor: 4.147

6.  Casual dimensions of college students' perceptions of physical symptoms.

Authors:  L C Swartzman; M C Lees
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7.  FAmily CEntered (FACE) advance care planning: Study design and methods for a patient-centered communication and decision-making intervention for patients with HIV/AIDS and their surrogate decision-makers.

Authors:  Allison L Kimmel; Jichuan Wang; Rachel K Scott; Linda Briggs; Maureen E Lyon
Journal:  Contemp Clin Trials       Date:  2015-06-02       Impact factor: 2.226

8.  Culture and gender diversity in commonsense beliefs about the causes of six illnesses.

Authors:  E A Klonoff; H Landrine
Journal:  J Behav Med       Date:  1994-08

9.  Personal models of osteoarthritis and their relation to self-management activities and quality of life.

Authors:  S E Hampson; R E Glasgow; A M Zeiss
Journal:  J Behav Med       Date:  1994-04

10.  The effect of physical, social and psychological factors on drug compliance in patients with mild hypertension.

Authors:  V S Okken; M G Niemeijer; A Dijkstra; M W Baars; S Said; K Hoogenberg; H Orfgen; S Otten; T J Cleophas
Journal:  Neth Heart J       Date:  2008-06       Impact factor: 2.380

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