Efficacy and safety of a simple home-based resistance exercise program for older adults with low muscle mass: a prospective longitudinal clinical trial

肌肉团 阻力训练 医学 物理疗法 临床试验 纵向研究 简单(哲学) 物理医学与康复 前瞻性队列研究 老年学 内科学 病理 认识论 哲学
作者
Vilai Kuptniratsaikul,Thanitta Thanakiatpinyo,Rinlada Pongratanakul,Pornsiri Chinsawangwattanakul,Ananya Srisomnuek,Suwicha Inthibal
出处
期刊:International Journal of Rehabilitation Research [Ovid Technologies (Wolters Kluwer)]
卷期号:44 (3): 241-247 被引量:2
标识
DOI:10.1097/mrr.0000000000000479
摘要

Low muscle mass is a common condition among older adults that adversely affects strength, physical performance and quality of life. This study aimed to investigate the efficacy and safety of a simple home-based resistance exercise program for older adults with low muscle mass, which was defined as appendicular skeletal mass (ASM) measured by bioimpedance analysis lower than 5.7 kg/m 2 in females, and lower than 7.0 kg/m 2 in males. This home-based resistance exercise program targets 10 muscles with a frequency of 3–5 days/week for 24 weeks. ASM, grip strength, gait speed and functional reach were measured at baseline, 3 and 6 months. The same four outcomes were then remeasured at 9 months to assess long-term effects. A total of 112 participants (average age: 70 years) were recruited. The mean difference between baseline and 6 months was statistically significant for all outcomes, including ASM [0.12 kg/m 2 : 95% confidence interval (CI), 0.05–0.18; P = 0.001], gait speed (0.19 meter/s: 95% CI, 0.14–0.25; P < 0.001), grip strength (2.06 kg: 95% CI, 1.32–2.80; P < 0.001), and functional reach distance (4.18 cm: 95% CI, 3.18–5.18; P < 0.001). Change over time for all main outcomes from baseline to 9 months also showed statistically significant improvement. The most commonly reported adverse events were muscle pain, joint pain and fatigue. The majority of participants (90–93%) had good exercise compliance, even at the end of the study. In conclusion, this 24-week simple home-based resistance exercise program significantly improved all main outcomes with low adverse events, and most participants continued the program after the end of the intervention.
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