Evaluation of Safety and Efficacy of ReHub in Patients Who Underwent Primary Total Knee Arthroplasty: Study Protocol for a Randomized Controlled Trial.

IF 1.1 Q3 SURGERY International Journal of Surgery Protocols Pub Date : 2021-04-19 DOI:10.29337/ijsp.138
Montse Nuevo, Hadis Mahdavi, Daniel Rodríguez, Teresa Faura, Núria Fabrellas, Simone Balocco, Marco Conti, Alessandro Castagna, Salvi Prat
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引用次数: 2

Abstract

Background: Total Knee Arthroplasty (TKA) is an intervention that can significantly improve the quality of life of patients with advanced knee osteoarthritis. Early start of rehabilitation and its continuation at home once the patient is discharged are key factors for the success of the process.This study aims to assess the effectiveness of a home-based telerehabilitation solution (ReHub) on improving functional capacity and clinical outcomes for patients who underwent TKA.

Methods/design: The study is a randomized, open-label with blinded outcome assessor, parallel assignment clinical trial with a sample size of 52 patients that is conducted according to the SPIRIT recommendations. After the TKA intervention, the patients are randomly allocated to the control group or the experimental group with a 1:1 ratio. Both groups follow a Fast Track recovery protocol which includes discharge after 2-3 days from surgery, a daily plan of 5 exercises for autonomous rehabilitation and domiciliary visits by a physiotherapist starting approximately 2 weeks after surgery. The experimental group uses the sensor-based telerehabilitation system ReHub to perform the exercises. The primary outcome measure is the range of motion of the knee. Secondary outcomes include physical performance, quality of life, pain intensity, muscle strength, treatment adherence and satisfaction with the ReHub system. The outcomes assessment is performed at hospital discharge (baseline), at stitch removal (2 weeks after baseline) and 2 weeks after stitch removal (4 weeks after baseline).The study conforms to the guidelines of the Declaration of Helsinki and was approved by the hospital's ethics committee.

Discussion: The study will address an important gap in the evidence base by reporting the effectiveness of an affordable and low-cost home-based telerehabilitation solution in patients who underwent TKA.

Ethics and dissemination: The study was approved by the hospital's ethics committee ("Comité Ético de Investigación Clínica del HCB", reg. HCB/2019/0571). The trial was registred at ClinicalTrials.gov (NCT04155957). The results of this study will be published in peer-reviewed journals as well as national and international conferences.

Trial registration: NCT04155957 (ClinicalTrials.gov).

Highlights: Assessing a home-based telerehabilitation solution effectiveness in knee surgery.In situations such as the CoVid-19 pandemic, it is a resolutive intervention method.Telerehabilitation is an alternative to conventional face-to-face physical therapy.This system is far less demanding in terms of human resources.Range of motion assessment is the primary outcome measure.

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评价ReHub在初次全膝关节置换术患者中的安全性和有效性:一项随机对照试验的研究方案。
背景:全膝关节置换术(TKA)是一种可以显著改善晚期膝关节骨关节炎患者生活质量的干预措施。患者出院后尽早开始康复并在家中继续康复是康复过程成功的关键因素。本研究旨在评估基于家庭的远程康复解决方案(ReHub)在改善TKA患者功能能力和临床结果方面的有效性。方法/设计:该研究是一项随机、开放标签、盲法结局评估、平行分配临床试验,样本量为52例患者,根据SPIRIT推荐进行。经TKA干预后,将患者按1:1的比例随机分为对照组和实验组。两组患者都遵循快速康复方案,包括术后2-3天后出院,每天5次自主康复锻炼计划,以及术后约2周开始由物理治疗师上门就诊。实验组使用基于传感器的远程康复系统ReHub进行练习。主要的结果测量是膝关节的活动范围。次要结局包括身体表现、生活质量、疼痛强度、肌肉力量、治疗依从性和对ReHub系统的满意度。结果评估在出院(基线)、拆线(基线后2周)和拆线后2周(基线后4周)进行。这项研究符合赫尔辛基宣言的指导方针,并得到了医院伦理委员会的批准。讨论:该研究将通过报告可负担和低成本的家庭远程康复解决方案对接受TKA的患者的有效性来解决证据基础上的一个重要空白。伦理和传播:该研究得到了医院伦理委员会(“comit Ético de Investigación Clínica del HCB”,reg)的批准。六氯苯/ 2019/0571)。该试验已在ClinicalTrials.gov注册(NCT04155957)。这项研究的结果将发表在同行评议的期刊以及国内和国际会议上。试验注册:NCT04155957 (ClinicalTrials.gov)。重点:评估基于家庭的远程康复解决方案在膝关节手术中的有效性。在CoVid-19大流行等情况下,这是一种果断的干预方法。远程康复是传统面对面物理治疗的另一种选择。这种制度对人力资源的要求要低得多。活动范围评估是主要的预后指标。
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期刊介绍: IJS Protocols is the first peer-reviewed, international, open access journal seeking to publish research protocols across across the full breadth of the surgical field. We are aim to provide rapid submission to decision times whilst maintaining a high quality peer-review process.
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