Advertisement
Research Article|Articles in Press, 104621

Healthcare utilisation and perceived healthcare accessibility and quality among people living with multiple sclerosis enrolled in an online course

      Highlights

      • Participants living with multiple sclerosis (MS) enrolled in an online course about MS reported being satisfied with their perceived healthcare quality and accessibility.
      • The number of healthcare visits, MS knowledge, health literacy, self-efficacy, and quality of life were all positively associated with perceived healthcare quality and accessibility in this cohort.
      • Participation in the Understanding MS massive open online course had no effect on healthcare utilization or perceived healthcare quality and accessibility.

      ABSTRACT

      Background

      People living with multiple sclerosis (MS) need access to high quality healthcare and support services. However, many people with MS do not have access to the services that they need.

      Objective

      To survey healthcare utilisation and perceived quality and accessibility among people living with MS who enrolled in a free online course about MS (the Understanding MS massive open online course (MOOC)) and to evaluate the impact of course completion on these outcomes.

      Methods

      This longitudinal cohort study evaluated participants before they began the course, immediately following completion, and six months following completion. We describe baseline healthcare utilisation and perceived accessibility and quality (N=813) and identify factors associated with satisfaction using chi-square and t-tests. We evaluate the impact of course completion among a sub-group (N=123) of participants who both completed the course and completed all three assessments using paired t-tests. We determined effect size using Cohen's D.

      Results

      Most participants accessed at least one healthcare service in the month before beginning the course and were satisfied with their healthcare accessibility and quality. Participants who reported being satisfied with their healthcare quality and accessibility had more healthcare visits, and greater MS knowledge, health literacy, quality of life and self-efficacy. Completing the Understanding MS MOOC had no effect on perceived healthcare accessibility or quality.

      Conclusion

      Our study suggests that people with MS who access online educational resources are likely to be well resourced in other areas as well. Our findings also suggest that a more targeted intervention may be necessary to improve healthcare accessibility and quality outcomes in people with MS.
      To read this article in full you will need to make a payment

      Purchase one-time access:

      Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online access
      One-time access price info
      • For academic or personal research use, select 'Academic and Personal'
      • For corporate R&D use, select 'Corporate R&D Professionals'

      Subscribe:

      Subscribe to Multiple Sclerosis and Related Disorders
      Already a print subscriber? Claim online access
      Already an online subscriber? Sign in
      Institutional Access: Sign in to ScienceDirect

      REFERENCES

        • Ahmad H
        • van der Mei I
        • Taylor BV
        • et al.
        Measuring the health-related quality of life in Australians with multiple sclerosis using the assessment of quality of ilfe-8-dimension (AQoL-8D) multi-attribute utility instrument.
        Mult Scler Rel Dis. 2020; 44102358
        • Asche CV
        • Singer ME
        • Jhaveri M
        • Chung H
        • Miller A.
        All-cause health care utilization and costs associated with newly diagnosed multiple sclerosis in the United States.
        Journal of Management Care Pharm. 2010; 16: 703-712
        • Bandura A.
        Self-efficacy: toward a unifying theory of behavioral change.
        Psychol Rev. 1977; 84: 191-215
        • Berkman ND
        • Sheridan SL
        • Donahue KE
        • Halpern DJ
        • Crotty K.
        Low health literacy and health outcomes: an updated systematic review.
        Ann Intern Med. 2011; 155: 97-107
      1. Bessing B, Honan C, van der Mei I, Taylor BV, Claflin SB. Evaluating the impact of the Understanding Multiple Sclerosis online course on participant MS knowledge, health literacy, resilience, self-efficacy, quality of life, and MS symptom severity. Accepted at MSARD.

        • Bessing B
        • Honan CA
        • van der Mei I
        • et al.
        Development and psychometric properties of the Multiple Sclerosis Knowledge Assessment Scale: Rasch analysis of a novel tool for evaluating MS knowledge.
        Mult Scler. 2020; https://doi.org/10.1177/1352458520929626
        • Cameron N
        An investigation of the psychometric properties of the Personal Wellbeing Index.
        Bachelor (Honours). School of Psychology, Deakin University, VIC, Australia2014
        • Chiu C
        • Bishop M
        • Pionke JJ
        • Strauser D
        • Santens RL.
        Barriers to the accessibility and continuity of health-care services in people with multiple sclerosis.
        International Journal of MS Care. 2017; 19: 313-321
        • Claflin SB
        • Klekociuk S
        • Fair H
        • Bostock E
        • Farrow M
        • Doherty K
        • Taylor BV.
        Assessing the impact of online health education interventions from 2010-2020: a systematic review of the evidence.
        American Journal of Health Promotion. 2022; 36: 201-224
        • Claflin SB
        • Klekociuk S
        • Campbell JA
        • Bessing B
        • van der Mei I
        • Taylor BV.
        Association between MS-related knowledge, health literacy, self-efficacy, and quality of life in a large cohort of MS community members: a cross-sectional study.
        MSARD. 2021; 54103158
        • Claflin SB
        • Gates R
        • Maher M
        • et al.
        Building a successful massive open online course (MOOC): A description of our process and lessons learned.
        J Med Int Res. 2020; 22: e16687
        • Cohen J.
        Statistical Power Analysis for the Behavioral Sciences.
        Routledge Academic, New York, NY1988
        • Dobson R
        • Giovannoni G.
        Multiple sclerosis – a review.
        European Journal of Neurology. 2019; 26: 27-40
        • Hadjigeorgiou G
        • Dardiotis E
        • Tsivgoulis G
        • Doskas T
        • Petrou D
        • Makris N
        • Vlaikidis N
        • Thomaidis T
        • Kyritsis A
        • Fakas N
        • Treska X
        • Karageorgiou C
        • Sotirli S
        • Giannoulis C
        • Papadimitriou D
        • Mylonas I
        • Kouremenos E
        • Vlachos G
        • Georgiopoulos D
        • Mademtzoglou D
        • Vikelis M
        • Zintzaras E.
        Observational study assessing demographic, economic, and clinical factors associated with access and utilization of health care services of patients with multiple sclerosis under treatment with interferon beta-1b (EXTAVIA).
        PLoS ONE. 2014; 9e113933
      2. International Society for Quality of Life Research (ISOQOL). What is Quality of life [Internet]. Accessed 3 May 2021. Available from: http://www.isoqol.org/about-isoqol/what-is-health-related-quality-of-life-research.

        • Lazar M
        • Davenport L.
        Barriers to health care access for low income families: a review of the literature.
        Journal of Community Health Nursing. 2018; 35: 28-37
        • Mauvais-Jarvis F
        • Merz NB
        • Barnes PJ
        • et al.
        Sex and gender: modifiers of health, disease, and medicine.
        Lancet. 2020; 396: 565-582
        • Mayo CD
        • Farzam-kia N
        • Ghahari S.
        Identifying barriers to and facilitators of health services access encountred by individuals with multiple sclerosis.
        International Journal of MS Care. 2021; 1: 39-44
        • Minden SL
        • Frankel D
        • Hadden L
        • Hoaglin DC.
        Access to health care for people with multiple sclerosis.
        Multiple Sclerosis. 2007; 13: 547-558
        • Osborne RH
        • Batterham RW
        • Elsworth GR
        • et al.
        The grounded psychometric development and initial validation of the Health Literacy Questionnaire (HLQ).
        BMC Public Health. 2013; 13: 658
        • Petrin J
        • Donnelly C
        • McColl M-A
        • Finlayson M.
        Is it worth it?: The experiences of person with multiple sclerosis as they access health care to manage their condition.
        Health Expectations. 2020; 23: 1269-1279
        • Ritter PL
        • Lorig K.
        The English and Spanish Self-Efficacy to Manage Chronic Disease Scale measures were validated using multiple studies.
        J Clin Epidemiol. 2014; 67: 1265-1273
        • Roddam H
        • Rog D
        • Janssen J
        • Wilson N
        • Cross L
        • Olajide O
        • Dey P.
        Inequalities in access to health and social care among adults with multiple sclerosis: a scoping review of the literature.
        Multiple Sclerosis and Related Disorders. 2019; 28: 290-304
        • Sørensen K
        • Van den Brouke S
        • Fullam J
        • et al.
        Health literacy and public health: a systematic review and integration of definitions and models.
        BMC Public Health. 2012; 12: 80