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基于移动健康平台的生活方式综合多组分运动在社区居住的虚弱前期老年人中的可行性、实用性和可接受性:一项短期、混合方法、前瞻性试点研究。

Feasibility, usability and acceptability of a lifestyle-integrated multicomponent exercise delivered via a mobile health platform in community-dwelling pre-frail older adults: a short-term, mixed-methods, prospective pilot study.

机构信息

The Shengli Clinical Medical College of Fujian Medical University, 134 Dongjie Road, Fuzhou, China.

Department of Nursing, Fujian Provincial Hospital, Fuzhou, China.

出版信息

BMC Geriatr. 2024 Nov 9;24(1):926. doi: 10.1186/s12877-024-05523-y.

DOI:10.1186/s12877-024-05523-y
PMID:39522035
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11549760/
Abstract

BACKGROUND

Pre-frailty is a window of opportunity for frailty reversal and can be enhanced by multicomponent exercise. The Lifestyle-integrated Functional Exercise (LiFE) program may be a promising alternative to overcome traditional exercise barriers. The latest advancements in mobile health (mHealth) technology have enabled individuals to retain the advantages of supervised exercise training within group settings while providing exercise programs that can be accessed and completed at home. This study aims to assess the feasibility, acceptability, and primary efficacy of the PF-Life program, which is the Lifestyle-Integrated Functional Exercise program for Pre-Frail supported by an mHealth platform.

METHODS

Sixteen pre-frail adults aged ≥ 65 years were recruited from five community health centers in Fuzhou, China. All participants were prescribed the PF-Life program by geriatricians using the mhealth platform (web-based portal). Participants engaged in the customized exercises program following in-app video instructions and feedback on the mhealth platform (smartphone application). Physical activity (PA) and sedentary behavior (SB) were registered daily through wearable devices. Study endpoints were feasibility (retention rate, compliance rate, adverse events), usability (system usability scale), acceptability (qualitative interviews), changes in physical function (timed up and go (TUG), handgrip strength (HGS), and 30-second chair rise tests), PA and SB.

RESULTS

The intervention was feasible, 88% of participants adhered completely to the study protocol, and 95% had completed at least 75% of the prescribed experimental duration. System usability was high (85 out of 100 best imaginable). Changes were observed from baseline to follow-up for total HGS (21.41 ± 6.38 vs. 24.12 ± 6.62 kg, P < 0.05, d = 0.714), TUG (8.23 ± 1.33 vs. 7.48 ± 2.01 s, P < 0.01, d = 1.647) and 30-second chair rise test (17.13 ± 4.3 vs. 20.04 ± 4.54 repetitions, P < 0.01, d = 0.94). In addition, SB decreased by a mean of 33 min/day (P < 0.01), and low physical activity increased by 31 min/day (P < 0.01). No adverse events occurred. The majority of participants found the PF-Life program to be straightforward, adaptable, and easily integrable into their daily routines.

CONCLUSIONS

Preliminary studies have demonstrated that the PF-life program exhibits good compliance, safety, and usability for the pre-frail elderly population. Large-scale randomized controlled trials are required to ascertain its long-term effectiveness.

摘要

背景

衰弱前期是衰弱逆转的机会窗口,可以通过多成分运动来增强。生活方式综合功能运动(LiFE)计划可能是克服传统运动障碍的一种很有前途的替代方法。移动健康(mHealth)技术的最新进展使个人能够在保留团体环境中监督运动训练的优势的同时,提供可以在家中访问和完成的运动计划。本研究旨在评估基于 mHealth 平台的支持生活方式综合功能运动(LiFE)计划的可行性、可接受性和初步疗效,该计划用于衰弱前期。

方法

从中国福州的五个社区卫生中心招募了 16 名年龄≥65 岁的衰弱前期成年人。所有参与者均由老年病学家使用 mHealth 平台(基于网络的门户)为其开出 PF-Life 计划。参与者根据 mHealth 平台(智能手机应用程序)中的应用内视频说明和反馈进行定制的锻炼计划。通过可穿戴设备每天记录身体活动(PA)和久坐行为(SB)。研究终点为可行性(保留率、依从率、不良事件)、可用性(系统可用性量表)、可接受性(定性访谈)、身体功能变化(计时起立行走测试(TUG)、握力(HGS)和 30 秒椅子上升测试)、PA 和 SB。

结果

该干预措施是可行的,88%的参与者完全遵守研究方案,95%的参与者完成了至少 75%的规定实验时间。系统可用性很高(满分 100 分,得 85 分)。与基线相比,随访时总握力(21.41±6.38 与 24.12±6.62 kg,P<0.05,d=0.714)、TUG(8.23±1.33 与 7.48±2.01 s,P<0.01,d=1.647)和 30 秒椅子上升测试(17.13±4.3 与 20.04±4.54 次,P<0.01,d=0.94)均有改善。此外,SB 减少了 33 分钟/天(P<0.01),低身体活动增加了 31 分钟/天(P<0.01)。没有发生不良事件。大多数参与者认为 PF-Life 计划简单明了、适应性强,并且很容易融入他们的日常生活。

结论

初步研究表明,PF-life 计划对衰弱前期老年人具有良好的依从性、安全性和可用性。需要进行大规模的随机对照试验来确定其长期疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae9b/11549760/baa9f6b4ddcf/12877_2024_5523_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae9b/11549760/42a2e42eb398/12877_2024_5523_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae9b/11549760/42a2e42eb398/12877_2024_5523_Fig1_HTML.jpg
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