Adherence, safety and potential effectiveness of a home-based Radio-Taiso exercise program in older adults with frailty: A pilot randomized controlled trial

被引:6
作者
Osuka, Yosuke [1 ,6 ]
Sasai, Hiroyuki [1 ]
Kojima, Narumi [1 ]
Sugie, Masamitsu [2 ]
Motokawa, Keiko [1 ]
Maruo, Kazushi [3 ]
Ono, Risa [4 ]
Aoyama, Toshihiko [4 ]
Inoue, Shigeru [5 ]
Kim, Hunkyung [1 ]
机构
[1] Tokyo Metropolitan Inst Gerontol, Res Team Promoting Independence & Mental Hlth, Itabashi Ku, Tokyo, Japan
[2] Tokyo Metropolitan Geriatr Hosp, Dept Cardiol, Itabashi Ku, Tokyo, Japan
[3] Inst Gerontol, Itabashi Ku, Tokyo, Japan
[4] Univ Tsukuba, Fac Med, Dept Biostat, Tsukuba, Japan
[5] Tokyo Med Univ, Dept Prevent Med & Publ Hlth, Shinjyuku Ku, Tokyo, Japan
[6] Tokyo Metropolitan Inst Gerontol, Res Team Promoting Independence & Mental Hlth, 35-2 Sakae Cho, Itabashi Ku, Tokyo 1730015, Japan
关键词
exercise; feasibility study; frailty; randomized controlled trial; safety; MEANINGFUL CHANGE; HEALTH; VALIDITY; PEOPLE;
D O I
10.1111/ggi.14511
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
AimRadio-Taiso, a traditional exercise program in Japan, may serve as a coping strategy for older adults with frailty during the COVID-19 pandemic. This phase II trial tested program adherence and safety and explored the potential effectiveness of a home-based Radio-Taiso. MethodsThis assessor-blind parallel randomized controlled trial included community-dwelling Jolder Japanese adults with frailty and pre-frailty. Fifty-eight eligible participants were randomly allocated to intervention and control groups. Intervention participants performed 3-5-min sessions of Radio-Taiso one to four times per day for 12 weeks. Feasibility criteria were set at practice and retention rates of >= 75%. Safety was monitored by assessing all adverse events reported by participants during the intervention period, irrespective of causality. Potential effectiveness was exploratorily assessed using items that allow clinical interpretation of changes: mobility and health-related quality of life (HR-QoL), assessed using the modified short physical performance battery (SPPB) and the SF-36, respectively. ResultsBoth practice (83%) and retention rates (100%) met the predetermined feasibility criteria. Eleven adverse events were reported but were supposedly unrelated to the intervention. In the intention-to-treat analysis, there was no clinically significant difference in the change in SPPB score between groups (-0.4 points, 95% confidence interval [CI], -1.2, 0.3); however, the intervention group scored higher in the mental component of HR-QoL than did the control group (3.4 points, 95% CI: -1.1, 7.8). ConclusionsThe preliminary data indicate that a phase III trial is feasible, focusing on the mental aspect of HR-QoL as the primary outcome. Geriatr Gerontol Int 2022; center dot center dot: center dot center dot-center dot center dot.
引用
收藏
页码:32 / 37
页数:6
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