Literature DB >> 22366934

[Restrictions in participation in women with fibromyalgia syndrome. An explorative pilot study].

A Ullrich1, E Farin, W H Jäckel.   

Abstract

BACKGROUND: Patients with fibromyalgia syndrome are often severely restricted in their ability to participate in everyday activities and in social interaction. The aim of this study was to document female patients' subjectively-perceived limitations in participation and to develop material to generate items for a specific participation questionnaire.
MATERIAL AND METHODS: We collected data from 8 groups of women with fibromyalgia syndrome (n=38), and developed a hierarchical system of categories using the patients' statements (ATLAS.ti; Qualitative Data Analysis).
RESULTS: Our final group of categories contains 10 superordinate categories. Women with fibromyalgia syndrome often describe restrictions in their relationships with other people, and the impaired ability to engage in social and leisure activities. They speak of difficulties at the workplace, while doing housework, and complain about a lack of understanding and awareness on the part of the general public.
CONCLUSION: Fibromyalgia syndrome patients admit to be extremely impaired in a variety of social roles. Their statements have enabled us to develop a questionnaire that reflects the range of factors restricting participation from the patient's perspective.

Entities:  

Mesh:

Year:  2012        PMID: 22366934     DOI: 10.1007/s00482-011-1123-3

Source DB:  PubMed          Journal:  Schmerz        ISSN: 0932-433X            Impact factor:   1.107


  17 in total

1.  Creating meaning in fibromyalgia syndrome.

Authors:  Sue Madden; Julius Sim
Journal:  Soc Sci Med       Date:  2006-09-01       Impact factor: 4.634

2.  The use of focus groups in rehabilitation research.

Authors:  Joseph Agan; Lynn C Koch; Phillip D Rumrill
Journal:  Work       Date:  2008

Review 3.  ["Teilhabe" (social participation) of patients in health care research: relations to similar concepts and overview of assessment instruments].

Authors:  E Farin
Journal:  Gesundheitswesen       Date:  2010-03-03

4.  Individuals' descriptions of living with fibromyalgia.

Authors:  Margaret Mui Cunningham; Carol Jillings
Journal:  Clin Nurs Res       Date:  2006-11       Impact factor: 2.075

5.  A qualitative exploration of carers' and 'patients' experiences of fibromyalgia: one illness, different perspectives.

Authors:  Karen Rodham; Nicola Rance; David Blake
Journal:  Musculoskeletal Care       Date:  2010-06

6.  Struggling for a tolerable existence: the meaning of men's lived experiences of living with pain of fibromyalgia type.

Authors:  Margareta Paulson; Ella Danielson; Siv Söderberg
Journal:  Qual Health Res       Date:  2002-02

7.  The Revised Fibromyalgia Impact Questionnaire (FIQR): validation and psychometric properties.

Authors:  Robert M Bennett; Ronald Friend; Kim D Jones; Rachel Ward; Bobby K Han; Rebecca L Ross
Journal:  Arthritis Res Ther       Date:  2009-08-10       Impact factor: 5.156

8.  PRO development: rigorous qualitative research as the crucial foundation.

Authors:  Kathryn Eilene Lasch; Patrick Marquis; Marc Vigneux; Linda Abetz; Benoit Arnould; Martha Bayliss; Bruce Crawford; Kathleen Rosa
Journal:  Qual Life Res       Date:  2010-05-30       Impact factor: 4.147

Review 9.  Religiousness and spirituality in fibromyalgia and chronic pain patients.

Authors:  Alexander Moreira-Almeida; Harold G Koenig
Journal:  Curr Pain Headache Rep       Date:  2008-10

10.  Illness experience in fibromyalgia syndrome: a metasynthesis of qualitative studies.

Authors:  Julius Sim; Sue Madden
Journal:  Soc Sci Med       Date:  2008-04-20       Impact factor: 4.634

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  2 in total

1.  Prevalence of Fibromyalgia in Pharmacy Professionals and Students: A Cross-Sectional Study.

Authors:  Shiekha S AlAujan; Haya M Almalag; Mohammed A Omair
Journal:  J Pain Res       Date:  2021-03-31       Impact factor: 3.133

2.  Participation and social functioning in patients with fibromyalgia: development and testing of a new questionnaire.

Authors:  Erik Farin; Antje Ullrich; Johannes Hauer
Journal:  Health Qual Life Outcomes       Date:  2013-08-05       Impact factor: 3.186

  2 in total

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