A Telemedicine Approach for Monitoring COPD: A Prospective Feasibility and Acceptability Cohort Study
- PMID: 36419950
- PMCID: PMC9677662
- DOI: 10.2147/COPD.S375049
A Telemedicine Approach for Monitoring COPD: A Prospective Feasibility and Acceptability Cohort Study
Abstract
Background: Telemedicine may help the detection of symptom worsening in patients with chronic obstructive pulmonary disease (COPD), potentially resulting in improved outcomes. This study aimed to determine the feasibility and acceptability of telemedicine among patients with COPD and physicians and facility staff in Japan.
Methods: This was a 52-week multicenter, prospective, single-arm, feasibility and acceptability cohort study of Japanese patients ≥40 years of age with COPD or asthma-COPD overlap. Participants underwent training to use YaDoc, a telemedicine smartphone App, which included seven daily symptom questions and weekly COPD Assessment Test (CAT) questions. The primary endpoint was participant compliance for required question completion. The secondary endpoint was participant and physician/facility staff acceptability of YaDoc based on questionnaires completed at Week 52. The impact of the Japanese COVID-19 pandemic state of emergency on results was also assessed.
Results: Of the 84 participants enrolled (mean age: 68.7 years, 88% male), 72 participants completed the study. Completion was high in the first six months but fell after that. Median (interquartile range [IQR]) compliance for daily questionnaire entry was 66.6% (31.0-91.8) and 81.0% (45.3-94.3) for weekly CAT entry. Positive participant responses to the exit questionnaire were highest regarding YaDoc ease of use (83.8%), positive impact on managing health (58.8%), and overall satisfaction (53.8%). Of the 26 physicians and facility staff enrolled, 24 completed the study. Of these, the majority (66.7%) responded positively regarding app facilitation of communication between physicians and participants to manage disease. Compliance was similar before and after the first COVID-19 state of emergency in Japan.
Conclusion: Daily telemedicine monitoring is potentially feasible and acceptable to both patients and physicians in the management of COPD. These results may inform potential use of telemedicine in clinical practice and design of future studies.
Clinical trial registration: JapicCTI-194916.
Keywords: Japan; acceptability; feasibility; patient-reported outcome measure; smartphone; telemonitoring.
© 2022 Shinoda et al.
Conflict of interest statement
No authors received payment for the development of the manuscript. Masahiro Shinoda, Osamu Hataji, Motohiko Miura, Masaharu Kinoshita, Akira Mizoo and Kazunori Tobino report having received grants from the GSK group of companies for the conduct of this study. Osamu Hataji also reports personal fees from AstraZeneca, Novartis Pharma, and Boehringer Ingelheim for research funding consulting fee, outside the submitted work. Yoko Shibata reports having received personal fees from the GSK group of companies during the conduct of the study, and lecture fees from AstraZeneca, Novartis and Boehringer Ingelheim. Takanobu Nishi is an employee of GSK. Takeo Ishii, Ryan Tomlinson, Taizo Matsuki and Paul W Jones are employees of GSK and hold stocks/shares. Bruce E. Miller, Toru Soutome and Ruth Tal-Singer are former employees at the time of the study and shareholders of GSK. Ruth Tal-Singer is a Board member of ENA Respiratory and holds stock options from ENA Respiratory, she reports honorarium for conference talks from AAAAI and ATS, travel reimbursement from AAAAI, and personal fees from Immunomet, VOCALIS Health, ENA Respiratory, and Teva until January 2021. The authors report no other conflicts of interest in this work.
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References
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- Global Initiative for Chronic Obstructive Lung Disease. Global strategy for the diagnosis, management and prevention of chronic obstructive pulmonary disease (2022 report); 2022. Available from: https://goldcopd.org/. Accessed November 4, 2022.
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