Cited by 28Multiple Sclerosis Research StudiesCancer survivorship and careHealth and Well-being Studies

Longitudinal Changes in Quality of Life and Related Psychosocial Variables in Australians with Multiple Sclerosis

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Wollin, Judy Ann, Spencer, Nancy, McDonald, Elizabeth, Fulcher, Gary, Bourne, Maureen, Simmons, Rex D.·2013·International Journal of MS Care

Abstract

This study explored changes in quality of life (QOL) and psychosocial variables in a large cohort of people with multiple sclerosis (MS). A total of 1287 Australians with MS were administered self-report questionnaires at baseline and 24 months later to examine the impact of disease severity and duration, perceived stress, self-efficacy, depression, and social support on QOL and self-care. Over the 2-year survey period, MS remained stable for 70% of respondents. Disease severity correlated with social support at baseline but not at 24 months, when the only significant correlation with disease severity was that of the World Health Organization Quality of Life-100 instrument (WHOQOL-100) domain of Level of Independence. Although QOL improved across the WHOQOL-100 domains Physical, Psychological, Level of Independence, Social Relationships, and Environment, decreases were found in the WHOQOL-100 facet overall QOL and well-being as well as self-efficacy over the same time period. Hierarchical multiple regression was used to assess the utility of four control measures. MS disease severity and MS disease duration were entered at Step 1, explaining 16.1% of the variance in QOL. After entry of perceived stress, self-efficacy, social support, and the Depression, Anxiety and Stress Scale-21 (DASS-21) at Step 2, the total variance explained by the model as a whole was 55.8% (F6,1028 = 216.495, P < .001). Thus, even in the presence of stable disease and improvement in some WHOQOL-100 domains, overall QOL and self-efficacy had decreased at 2 years after the collection of baseline data. Loss of self-efficacy, increased stress, and depression are key factors in reduced QOL in people with MS.

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Research works printed but not linked: 2

  1. Braden CJ. Learned self-help response to chronic illness. Sch Inq Nurs Pract. 1990;4:23-41.
  2. Sadovnick AD, Remick RA, Allen J, et al. Depression and multiple scle- rosis. Neurology. 1996;46:628-632.

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Authors
Wollin, J. A., Spencer, N., McDonald, E., Fulcher, G., Bourne, M., & Simmons, R. D.
Affiliations
Griffith University (AU)
Venue
International Journal of MS Care
Published
2013-06-01
Volume
15
Issue
2
Pages
90-97
ISSN
1537-2073 (ISSN-L)
OpenAlex
W2073687938
Cited by
28
References
32
Citations by year
2026: 2 · 2025: 2 · 2024: 1 · 2023: 4 · 2022: 3 · 2021: 5 · 2020: 2 · 2018: 4 · 2016: 3 · 2015: 1 · 2014: 1
FWCI
1.25
Type
journal article
Language
en
Open access
Locations
  • International Journal of MS Care (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • Griffith Research Online (submittedVersion)
Funders
Multiple Sclerosis Australia
Topics
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Multiple Sclerosis Research Studies
  • Health Sciences › Medicine › Oncology › Cancer survivorship and care
  • Social Sciences › Psychology › Clinical Psychology › Health and Well-being Studies
Keywords
multiple sclerosis, quality of life, psychosocial factors, disease severity, disease duration, perceived stress, self-efficacy, depression, social support, self-care, WHOQOL-100, longitudinal change, well-being

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