Literature DB >> 10558325

Sense making in multiple sclerosis: the information needs of people during an acute exacerbation.

L M Baker1.   

Abstract

Chronic illness has been described as a major disruption in one's everyday life. Studies have shown that people seek and use information to help them cope with their disease. Using the micro-moment time-line interview technique, this study focused on the information needs of people with multiple sclerosis (MS) who had recently experienced an exacerbation of their disease. The results revealed gaps in people's knowledge about physical symptoms they were experiencing, emotions they felt, and drugs. Various sources of and barriers to obtaining information were identified. The results suggest that health professionals need to be aware of the continuing need for relevant, current, and specific information to help people with MS retain their independence and to empower them to make informed decisions.

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Year:  1998        PMID: 10558325     DOI: 10.1177/104973239800800108

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


  12 in total

1.  Theories for practitioners: two frameworks for studying consumer health information-seeking behavior.

Authors:  L M Baker; K E Pettigrew
Journal:  Bull Med Libr Assoc       Date:  1999-10

2.  General health problems of inner-city sex workers: a pilot study.

Authors:  Lynda M Baker; Patricia Case; Deena L Policicchio
Journal:  J Med Libr Assoc       Date:  2003-01

3.  Validation of the Comprehensive International Classification of Functioning, Disability, and Health Core Set for multiple sclerosis from the perspective of physicians.

Authors:  Stephanie Berno; Michaela Coenen; Andreas Leib; Alarcos Cieza; Jürg Kesselring
Journal:  J Neurol       Date:  2012-01-24       Impact factor: 4.849

4.  An assessment of the feasibility and utility of the MS symptom and impact diary (MSSID).

Authors:  Joanne Greenhalgh
Journal:  Qual Life Res       Date:  2005-06       Impact factor: 4.147

5.  One size does not fit all: using qualitative methods to inform the development of an Internet portal for multiple sclerosis patients.

Authors:  Ashish Atreja; Neil Mehta; Deborah Miller; Shirley Moore; Karen Nichols; Holly Miller; C Martin Harris
Journal:  AMIA Annu Symp Proc       Date:  2005

6.  The path to self-management: a qualitative study involving older people with multiple sclerosis.

Authors:  Michelle Ploughman; Mark W Austin; Michelle Murdoch; Anne Kearney; Marshall Godwin; Mark Stefanelli
Journal:  Physiother Can       Date:  2012-01-31       Impact factor: 1.037

7.  Perception of quality and trustworthiness of Internet resources by personal health information seekers.

Authors:  P Zoë Stavri; Donna J Freeman; Catherine M Burroughs
Journal:  AMIA Annu Symp Proc       Date:  2003

8.  Exploring the personal reality of disability and recovery: a tool for empowering the rehabilitation process.

Authors:  Ashley E Kurz; Nicole Saint-Louis; Janice P Burke; Margaret G Stineman
Journal:  Qual Health Res       Date:  2008-01

9.  Online health information seeking: how people with multiple sclerosis find, assess and integrate treatment information to manage their health.

Authors:  Anneliese J Synnot; Sophie J Hill; Kerryn A Garner; Michael P Summers; Graziella Filippini; Richard H Osborne; Sue D P Shapland; Cinzia Colombo; Paola Mosconi
Journal:  Health Expect       Date:  2014-08-28       Impact factor: 3.377

10.  The study circle as a tool in multiple sclerosis patient education in Sweden.

Authors:  Anne-Marie Landtblom; Cecilia Lang; Gullvi Flensner
Journal:  Patient Prefer Adherence       Date:  2008-02-02       Impact factor: 2.711

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