自主评估站和个性化训练算法对久坐成人生活质量和体能的影响:随机对照试验。

IF 2 Q3 HEALTH CARE SCIENCES & SERVICES
Yann Le Mat, Corentin Casali, Franck Le Mat, Léonard Féasson, Clément Foschia, Mathias Géry, Jérémy Rossi, Guillaume Y Millet
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引用次数: 0

摘要

背景:缺乏运动是非传染性疾病的一个主要风险因素,也是导致过早死亡的一个主要原因。世界卫生组织(WHO)建议,无论年龄、性别或个人习惯如何,每周至少进行 150 分钟中等强度的体育锻炼(PA)。然而,在运动表现和临床环境中,个性化训练(PT)方案已显示出优于一般指南的功效:我们假设,与遵循世界卫生组织的建议相比,根据初步身体评估结果制定的自动运动训练计划将提高整体生活质量、睡眠质量和体能,并减少疲劳和抑郁:这项为期 5 个月的单盲随机对照试验涉及 112 名久坐不动或运动量极少的参与者,他们被随机分为运动训练组和自由训练(FT)组。对两组参与者的体能以及生活质量、睡眠、抑郁和疲劳等主观指标进行评估。1 个月后,两组被要求在 4 个月内每周进行 150 分钟的体育锻炼;体育锻炼组可以跟随手机应用程序上的 "虚拟教练 "进行一些个性化的体育锻炼,也可以按照自己的意愿进行,而自由训练组则要遵循世界卫生组织的一般体育锻炼建议:结果:我们没有发现任何组别与时间之间在运动时间或强度、身体素质和主观测量方面的交互作用。然而,如果将两组放在一起考虑,则在 PA 持续时间方面存在显著的测试前和测试后时间效应(PA 持续时间为 18.2 分钟 vs 24.5 分钟/天;P2max 为 26.8 vs 29 mL min-1 kg-1;P2;P2;P=.048)。最后,在综合考虑 PT 组和 FT 组的情况下,使用 12 项简表健康调查,生活质量的心理部分从测试前到测试后都有显著改善(41.9 vs 46.0;PC 结论:个性化培训并不比一般建议更有效。对于久坐不动或缺乏运动的人来说,稍微增加运动量(从 18 分钟/天增加到 24 分钟/天)就足以显著提高体能,并显著改善生活质量、幸福感、抑郁和疲劳:试验注册:ClinicalTrials.gov NCT04998266;https://clinicaltrials.gov/study/NCT04998266。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of a Self-Autonomous Evaluation Station and Personalized Training Algorithm on Quality of Life and Physical Capacities in Sedentary Adults: Randomized Controlled Trial.

Background: Physical inactivity is a major risk factor for noncommunicable diseases and a leading cause of premature death. The World Health Organization (WHO) recommends at least 150 minutes of moderate intensity physical activity (PA) weekly, regardless of age, gender, or personal habits. However, in both sports performance and clinical settings, personalized training (PT) regimens have shown superior efficacy over general guidelines.

Objective: We hypothesized that an automatic PT program, informed by initial physical evaluations, would increase overall quality of life, quality of sleep, and physical capabilities and reduce fatigue and depression compared with adherence to WHO recommendations.

Methods: This 5-month, randomized, single-blinded controlled trial involved 112 sedentary or minimally active participants, divided randomly into PT and free training (FT) groups. Physical capabilities and subjective measures such as quality of life, sleep, depression, and fatigue were evaluated for both groups. After 1 month, both groups were asked to perform 150 minutes of PA per week for 4 months; the PT group could either follow a "virtual coach" on a mobile app to follow some personalized PA or do what they would like, while the FT group was to follow the general PA recommendations of the WHO.

Results: We did not find any group×time interaction for PA duration or intensity, physical qualities, and subjective measures. However, considering both groups together, there was a significant pretest and posttest time effect for duration of PA (18.2 vs 24.5 min/d of PA; P<.001), intensity (2.36 vs 3.11; P<.001), and workload (46.8 vs 80.5; P<.001). Almost all physical qualities were increased pretest and posttest (ie, estimated VO2max 26.8 vs 29 mL min-1 kg-1; P<.001; flexibility 25.9 vs 26.9 cm; P=.049; lower limb isometric forces 328 vs 347 N m; P=.002; reaction time 0.680 vs 0.633 s; P<.001; power output on cyclo-ergometer 7.63 vs 7.82 W; P<.003; and balance for the left and right leg 215 vs 163 mm2; P<.003 and 186 vs 162 mm2; P=.048, respectively). Finally, still considering the PT and FT groups together, there were significant pretest to posttest improvements in the mental component of quality of life using the 12-item Short Form Health Survey (41.9 vs 46.0; P<.006), well-being using the Warwick-Edinburgh Mental Well-Being Scale (48.3 vs 51.7; P<.002), depression using the Center for Epidemiologic Studies Depression Scale (15.5 vs 11.5; P=.02), and fatigue using the Functional Assessment of Chronic Illness Therapy-Fatigue (37.1 vs 39.5; P=.048).

Conclusions: The individualized training was not more effective than the general recommendations. A slight increase in PA (from 18 to 24 min/d) in sedentary or poorly active people is enough for a significant increase in physical capabilities and a significant improvement in quality of life, well-being, depression, and fatigue.

Trial registration: ClinicalTrials.gov NCT04998266; https://clinicaltrials.gov/study/NCT04998266.

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来源期刊
JMIR Formative Research
JMIR Formative Research Medicine-Medicine (miscellaneous)
CiteScore
2.70
自引率
9.10%
发文量
579
审稿时长
12 weeks
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