Efficacy of the mHealth-Based Exercise Intervention re.flex for Patients With Knee Osteoarthritis: Pilot Randomized Controlled Trial.

IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES JMIR mHealth and uHealth Pub Date : 2024-09-09 DOI:10.2196/54356
Valerie Dieter, Pia Janssen, Inga Krauss
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Abstract

Background: Exercise therapy is recommended by international guidelines as a core treatment for patients with knee osteoarthritis. However, there is a significant gap between recommendations and practice in health care. Digital exercise apps are promising to help solve this undersupply.

Objective: This study aims to evaluate the efficacy of a 12-week fully automated app-based exercise intervention with and without a supporting knee brace on health-related outcomes, performance measures, and adherence in patients with knee osteoarthritis.

Methods: This closed user group trial included participants with moderate to severe unicondylar painful knee osteoarthritis. Randomization was 1:1:2 into an intervention group (IG) with 2 subgroups (app-based training [IG A] and app-based training and a supportive knee brace [IG AB]) and a control group (CG). The intervention included a 12-week home exercise program with 3 sessions per week. Instructions for the exercises were given via the app and monitored using 2 accelerometers placed below and above the affected knee joint. Participants in the CG did not receive any study intervention but were allowed to make use of usual care. Osteoarthritis-specific pain (Knee Injury and Osteoarthritis Outcome Score) was defined as the primary outcome, and secondary outcomes included all other Knee Injury and Osteoarthritis Outcome Score subscales, general health-related quality of life (Veterans RAND 12-item Health Survey), psychological measures (eg, exercise self-efficacy), performance measures (strength and postural control), and the monitoring of adherence and safety. Outcomes were assessed at baseline and after 12 weeks. Intervention effects were calculated using baseline-adjusted analysis of covariance for the joint comparison of IG A and IG AB versus the CG using a per-protocol approach. Subgroup analyses were conducted for each IG separately.

Results: A total of 61 participants were included (IG: n=30, 49%; CG: n=31, 51%; male: n=31, 51%; female: n=30, 49%; mean age 62.9, SD 8.5 years; mean BMI 27.7, SD 4.5 kg/m2). Analysis revealed statistically significant effects in favor of the IG for pain reduction (P<.001; effect size [ES]=0.76), improvements in physical function (P<.001; ES=0.64), improvements in symptoms (P=.01; ES=0.53), improvements in sport and recreation activities (P=.02; ES=0.47), improvements in knee-related quality of life (P<.001; ES=0.76), and improvements in the physical component of general health-related quality of life (P<.001; ES=0.74). Mean differences ranged from 6.0 to 13.2 points (scale range 0-100). ESs indicated small to medium effects. No effects were found for psychological and performance measures. Participants adhered to 92.5% (899/972) of all scheduled exercise sessions.

Conclusions: Individuals with knee osteoarthritis undergoing a 12-week sensor-assisted app-based exercise intervention with or without an additional knee brace experienced clinically meaningful treatment effects regarding pain relief and improvements in physical function as well as other osteoarthritis-specific concerns compared to controls.

Trial registration: German Clinical Trials Register (DRKS) DRKS00023269; https://drks.de/search/de/trial/DRKS00023269.

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基于移动医疗的膝骨关节炎患者运动干预 re.flex 的疗效:试点随机对照试验。
背景:国际指南建议将运动疗法作为膝关节骨性关节炎患者的核心治疗方法。然而,建议与医疗实践之间存在巨大差距。数字运动应用程序有望帮助解决这一供应不足的问题:本研究旨在评估一种为期 12 周、基于应用程序的全自动运动干预措施的疗效,该干预措施可使用或不使用支撑型护膝,对膝关节骨性关节炎患者的健康相关结果、表现指标和坚持性均有影响:这项封闭式用户组试验的参与者包括中度至重度单髁疼痛性膝关节骨关节炎患者。以 1:1:2 的比例随机分为干预组(IG)和对照组(CG),前者包含两个子组(基于应用程序的训练 [IG A]、基于应用程序的训练和支持性膝关节支架 [IG AB])。干预措施包括为期 12 周的家庭锻炼计划,每周 3 次。运动指导通过应用程序进行,并使用放置在受影响膝关节下方和上方的两个加速度计进行监测。CG参与者不接受任何研究干预,但可利用常规护理。骨关节炎特异性疼痛(膝关节损伤和骨关节炎结果评分)被定义为主要结果,次要结果包括所有其他膝关节损伤和骨关节炎结果评分分量表、一般健康相关生活质量(退伍军人兰德12项健康调查)、心理测量(如运动自我效能)、表现测量(力量和姿势控制)以及对坚持性和安全性的监测。结果在基线和 12 周后进行评估。对于 IG A 和 IG AB 与 CG 的联合比较,采用基线调整后的协方差分析计算干预效果,并按协议方法进行。对每种 IG 分别进行了分组分析:共纳入 61 名参与者(IG:n=30,49%;CG:n=31,51%;男性:n=31,51%;女性:n=30,49%;平均年龄 62.9 岁,SD 8.5 岁;平均体重指数 27.7,SD 4.5 kg/m2)。分析表明,IG 在减轻疼痛方面的效果具有统计学意义(结论:IG 对膝关节骨性关节炎患者有明显的疗效:与对照组相比,膝关节骨性关节炎患者在接受为期12周的基于传感器辅助应用程序的运动干预后,无论是否使用额外的护膝,都能在缓解疼痛、改善身体功能以及其他骨性关节炎特定问题方面获得有临床意义的治疗效果:试验注册:德国临床试验注册中心(DRKS)DRKS00023269;https://drks.de/search/de/trial/DRKS00023269。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JMIR mHealth and uHealth
JMIR mHealth and uHealth Medicine-Health Informatics
CiteScore
12.60
自引率
4.00%
发文量
159
审稿时长
10 weeks
期刊介绍: JMIR mHealth and uHealth (JMU, ISSN 2291-5222) is a spin-off journal of JMIR, the leading eHealth journal (Impact Factor 2016: 5.175). JMIR mHealth and uHealth is indexed in PubMed, PubMed Central, and Science Citation Index Expanded (SCIE), and in June 2017 received a stunning inaugural Impact Factor of 4.636. The journal focusses on health and biomedical applications in mobile and tablet computing, pervasive and ubiquitous computing, wearable computing and domotics. JMIR mHealth and uHealth publishes since 2013 and was the first mhealth journal in Pubmed. It publishes even faster and has a broader scope with including papers which are more technical or more formative/developmental than what would be published in the Journal of Medical Internet Research.
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