scholarly journals “Sounds a Bit Crazy, But It Was Almost More Personal:” A Qualitative Study of Patient and Clinician Experiences of Physical Therapist-Prescribed Exercise For Knee Osteoarthritis Via Skype

2017 ◽  
Vol 69 (12) ◽  
pp. 1834-1844 ◽  
Author(s):  
R. S. Hinman ◽  
R. K. Nelligan ◽  
K. L. Bennell ◽  
C. Delany
2013 ◽  
Vol 23 (2-03) ◽  
pp. 223-240 ◽  
Author(s):  
Chuan Silvia Li ◽  
Rubini Pathy ◽  
Anthony Adili ◽  
Victoria Avram ◽  
Mohamed A. Barasi ◽  
...  

2021 ◽  
Author(s):  
Elizabeth C. Lavender ◽  
Anna M. Anderson ◽  
Esther Dusabe‐Richards ◽  
Deborah Antcliff ◽  
Sarah R. Kingsbury ◽  
...  

2011 ◽  
Vol 91 (6) ◽  
pp. 906-919 ◽  
Author(s):  
Pauline M. Masley ◽  
Carey-Leah Havrilko ◽  
Mark R. Mahnensmith ◽  
Molly Aubert ◽  
Diane U. Jette

2013 ◽  
Vol 6 (1) ◽  
Author(s):  
Abdullah Al-Taiar ◽  
Reem Al-Sabah ◽  
Ehab Elsalawy ◽  
Dia Shehab ◽  
Shaima Al-Mahmoud

2021 ◽  
Author(s):  
Jenny Leese ◽  
Graham MacDonald ◽  
Catherine L Backman ◽  
Anne Townsend ◽  
Laura Nimmon ◽  
...  

BACKGROUND Current evidence indicates physical activity wearables could support persons with knee osteoarthritis (OA) to be more physically active. Recent evidence also identifies, however, some persons with arthritis experience guilt or worry while using a wearable if they are not as active as they feel they should be. Questions remain around how persons with knee OA experience benefits or downsides in using a wearable in their everyday lives. Better understanding is needed if wearables are to be incorporated in arthritis self-management in ways that are ethically aware. OBJECTIVE Using an ethics lens, describe a range of experiences from persons with knee OA who used a wearable during a physical activity counselling intervention study. METHODS This is a secondary analysis of qualitative interviews (60-90 mins) nested within a randomized controlled trial (RCT). Guided by phenomenography, we explored the experiences of persons with knee OA, following participation in a physical activity counselling intervention. The intervention consisted of a 1.5-hour education session about physical activity, using a Fitbit Flex, and receiving 4 biweekly phone calls for activity counselling with a study physiotherapist (PT) in an 8-week period. All PTs were trained in the Brief Action Planning approach, whereby they guided participants to identify activity goals, develop an action plan, and identify barriers and solutions. Benefits or downsides experienced in participants’ relationships with themselves or the study PT when using the wearable were identified using a relational ethics lens. RESULTS Interviews with 21 participants (12 females, 9 males) aged 40-82 years were analyzed. Education ranged from high school graduate (n=4) to bachelor’s degree or above (n=11). Three categories of description were identified: 1) Participants experienced their wearable as a motivating or nagging influence to be more active, depending on how freely they were able to make autonomous choices about physical activity in their everyday lives; 2) Some participants felt a sense of accomplishment from seeing progress in their wearable data, which fuelled motivation. One participant experienced negative emotions (e.g., self-blame) if his wearable data indicated physical activity goals were not met; 3) For some participants, sharing wearable data helped to build mutual trust in their relationship with the study PT. They also expressed, however, there was potential for sharing wearable data to undermine this trust, particularly if this data was inaccurate. CONCLUSIONS To our knowledge, this is the first qualitative study that uses a relational ethics lens to explore how persons with arthritis experienced changes in their relationship with a health professional when using a wearable during research participation. Findings also provide an early glimpse into positive and negative emotional impacts of using a wearable that can be experienced by participants with knee OA when participating in an RCT to support physical activity.


2020 ◽  
Vol 21 (1) ◽  
Author(s):  
Wen-Ling Yeh ◽  
Yun-Fang Tsai ◽  
Kuo-Yao Hsu ◽  
Dave Weichih Chen ◽  
Jong-Shyan Wang ◽  
...  

2019 ◽  
Vol 27 (4) ◽  
pp. 346-356 ◽  
Author(s):  
Josephine S.F. Chow ◽  
Veronica Eugenia Gonzalez-Arce ◽  
Andrew Knight ◽  
Nutan Maurya ◽  
Friedbert Kohler

Purpose A recent study on the implementation of telemonitoring has provided an opportunity to explore how telemonitoring could be further developed to enhance better patient, carer and clinician experiences for patients living with chronic disease. The purpose of this paper is to identify the challenges and lessons of the telemonitoring implementation and to identify strategies to inform future implementation. Design/methodology/approach A qualitative study was conducted with a purposive sample using semi-structured interviews to explore their views about the issues identified in the research aims. Interview themes were informed by current literature and the findings from local studies. Interviews were recorded, transcribed verbatim and analyzed thematically. Findings A total of 16 participants were interviewed. Overall the recruitment of 56 percent were from identified potential participants. Five core themes were identified, linking different aspects of the telemonitoring implementation: impact of telemonitoring; implementation and management lessons; program risks; program main changes from beginning; and future strategies and recommendations. Originality/value This study will inform the wider roll out of telemonitoring across the region with the goal of ensuring future interventions achieve better clinical outcomes, patient, carer experience and deliver better value.


2019 ◽  
Vol 27 ◽  
pp. S298-S299
Author(s):  
S. Bunzli ◽  
P. O'Brien ◽  
D. Ayton ◽  
M. Dowsey ◽  
J. Gunn ◽  
...  

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