期刊
DISABILITY AND REHABILITATION
卷 45, 期 7, 页码 1147-1153出版社
TAYLOR & FRANCIS LTD
DOI: 10.1080/09638288.2022.2055159
关键词
Telerehabilitation; multiple sclerosis (MS); physiotherapy; exercise; patient preference; internet-based intervention
This study aims to share the perspectives of people living with MS and physiotherapists on their experiences in a randomized clinical trial of online physiotherapy versus an active comparator. The results show that while the online physiotherapy platform is useful for supporting exercise, there are limitations in terms of usability and utility. The needs of people with moderate to severe MS should be considered, especially with the increasing popularity of online platforms during the pandemic.
Purpose There is a gap in research on how best to support exercise in moderate to severe MS. The objective of this study is to share perspectives of people living with MS and physiotherapists on their experiences in a randomized clinical trial of online physiotherapy vs. an active comparator. Methods Semi-structured exit interviews were conducted with volunteer participants from the online and comparator arms of the trial, and focus groups were held with study physiotherapists. Transcripts were analyzed using reflexive thematic analysis. Results Perspectives from participants with MS yielded three themes: usability of their program, utility of their program, and motivation to participate. Visual and dexterity impairments limited the usability of the online program. Having an opportunity to be pushed was valued by participants in both trial arms. Motivation to exercise was variable, and participants desired periodic face-to-face contact with their physiotherapists. Perspectives from trial physiotherapists yielded similar and complementary findings concerning usability and utility. Conclusions Participants with MS and physiotherapists found the online physiotherapy platform useful for supporting exercise, yet they identified some limitations. As the appeal of online platforms has increased since the pandemic, it will be important to consider the needs of people with moderate to severe MS.
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