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首页> 外文期刊>JMIR mHealth and uHealth >Assessing the Impact of a Novel Smartphone Application Compared With Standard Follow-Up on Mobility of Patients With Knee Osteoarthritis Following Treatment With Hylan G-F 20: A Randomized Controlled Trial
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Assessing the Impact of a Novel Smartphone Application Compared With Standard Follow-Up on Mobility of Patients With Knee Osteoarthritis Following Treatment With Hylan G-F 20: A Randomized Controlled Trial

机译:评估新型智能手机应用与标准随访相比对Hylan G-F 20治疗后膝骨关节炎患者活动性的影响:一项随机对照试验

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Background Osteoarthritis (OA) is a leading cause of disability in the United States. Although no disease-modifying therapies exist, patients with knee OA who increase walking may reduce risk of functional limitations. Objective The objective of the study is to evaluate the impact of a mobile app (OA GO) plus wearable activity monitor/pedometer (Jawbone UP 24) used for 90 days on the mobility of patients with knee OA treated with hylan G-F 20. Methods Patients with knee OA aged 30 to 80 years who were eligible to receive hylan G-F 20 and were familiar with smartphone technology were enrolled in this randomized, multicenter, open-label study. Patients who had a body mass index above 35 kg/m2 were excluded. All patients received a single 6-mL injection of hylan G-F 20 and wore the Jawbone monitor. The patients were then randomized 1:1 to Jawbone and OA GO (Group A; n=107) with visible feedback (unblinded) or Jawbone only (Group B; n=104) with no visible feedback (blinded). The primary endpoint was mean change from baseline in steps per day at day 90 between Groups A and B. Results Baseline characteristics were similar between groups. There were significant differences between the increases in least squares (LS) mean number of steps per day (1199 vs 467, P =.03) and the mean percentage change (35.8% vs 11.5%, P =.02) from baseline in favor of Group A over Group B. There was a greater reduction in pain from baseline during the 6-minute walk test in Group A versus Group B. (LS mean change: ?55.3 vs ?33.8, P =.007). Most patients (65.4%) and surveys of physicians (67.3%) reported they would be likely or very likely to use/recommend the devices. Patient Activity Measure-13 scores improved from baseline (LS mean change for Groups A and B: 5.0 vs 6.9), with no significant differences between groups. The occurrence of adverse events was similar in the 2 groups. Conclusions Use of a novel smartphone app in conjunction with a wearable activity monitor provided additional improvement on mobility parameters such as steps per day and pain with walking in the 6-minute walk test in patients with knee OA who were treated with hylan G-F 20. Results also highlight the amenability of patients and physicians to using mobile health technology in the treatment of OA and suggest further study is warranted.
机译:背景技术骨关节炎(OA)是美国致残的主要原因。尽管尚无改善疾病的疗法,但步行增加的膝骨OA患者可能会降低功能受限的风险。目的本研究的目的是评估使用移动应用程序(OA GO)和可穿戴活动监测器/计步器(Jawbone UP 24)进行90天治疗对经hylan GF 20治疗的膝关节炎患者的活动性的影响。这项随机,多中心,开放标签的研究纳入了年龄在30至80岁之间且有资格接受hylan GF 20并熟悉智能手机技术的膝OA的患者。排除体重指数高于35 kg / m 2 的患者。所有患者均单次注射6 mL的Hylan G-F 20,并佩戴Jawbone监护仪。然后将患者按1:1比例随机分配到有可见反馈(无盲)的Jawbone和OA GO(A组; n = 107)或无可见反馈(无盲)的仅Jawbone(B组; n = 104)。主要终点是在A组和B组之间在第90天每天基线的平均变化。结果组之间的基线特征相似。每天的最小二乘(LS)平均步数增加(1199 vs 467,P = .03)与相对于基线的平均百分比变化(35.8%vs 11.5%,P = .02)之间存在显着差异与B组相比,A组在6分钟的步行测试中疼痛从基线减轻的幅度更大(LS平均变化:?55.3 vs?33.8,P = .007)。大多数患者(65.4%)和医生调查(67.3%)报告说,他们很可能或非常可能会使用/推荐该设备。患者活动度量13得分较基线水平有所提高(A组和B组的LS平均变化:5.0对6.9),各组之间无显着差异。两组的不良事件发生率相似。结论将新型智能手机应用程序与可穿戴式活动监视器配合使用,可在接受Hylan GF 20治疗的OA膝关节患者中进行6分钟步行测试,从而进一步改善移动性参数,例如每天步数和步行时的疼痛。还强调了患者和医生使用移动医疗技术治疗OA的能力,并建议进一步研究。

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