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Shoe-stiffening inserts for first metatarsophalangeal joint osteoarthritis (the SIMPLE trial): study protocol for a randomised controlled trial

机译:用于第一次跖趾关节骨关节炎(简单试验)的鞋状刀片:用于随机对照试验的研究方案

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摘要

Abstract Background This article describes the design of a parallel-group, participant- and assessor-blinded randomised controlled trial comparing the effectiveness of shoe-stiffening inserts versus sham shoe insert(s) for reducing pain associated with first metatarsophalangeal joint (MTPJ) osteoarthritis (OA). Methods Ninety participants with first MTPJ OA will be randomised to receive full-length shoe-stiffening insert(s) (Carbon Fibre Spring Plate, Paris Orthotics, Vancouver, BC, Canada) plus rehabilitation therapy or sham shoe insert(s) plus rehabilitation therapy. Outcome measures will be obtained at baseline, 4, 12, 24 and 52 weeks; the primary endpoint for assessing effectiveness being 12 weeks. The primary outcome measure will be the foot pain domain of the Foot Health Status Questionnaire (FHSQ). Secondary outcome measures will include the function domain of the FHSQ, severity of first MTPJ pain (using a 100-mm Visual Analogue Scale), global change in symptoms (using a 15-point Likert scale), health status (using the Short-Form-12® Version 2.0 and EuroQol (EQ-5D-5L™) questionnaires), use of rescue medication and co-interventions, self-reported adverse events and physical activity levels (using the Incidental and Planned Activity Questionnaire). Data will be analysed using the intention-to-treat principle. Economic analysis (cost-effectiveness and cost-utility) will also be performed. In addition, the kinematic effects of the interventions will be examined at 1 week using a three-dimensional motion analysis system and multisegment foot model. Discussion This study will determine whether shoe-stiffening inserts are a cost-effective intervention for relieving pain associated with first MTPJ OA. The biomechanical analysis will provide useful insights into the mechanism of action of the shoe-stiffening inserts. Trial registration Australian New Zealand Clinical Trials Registry, identifier: ACTRN12616000552482 . Registered on 28 April 2016.
机译:摘要背景本文介绍了并行组,参与者和抑制的随机对照试验的设计比较了鞋加强刀片与假鞋插入物的有效性,用于减少与第一个跖趾关节(MTPJ)骨关节炎相关的疼痛( OA))。方法采用第一个MTPJ OA的九十名参与者将随机分配以接收全长鞋加强刀片(碳纤维弹簧板,巴黎矫形器,温哥华,BC,加拿大)加康复治疗或假鞋插入加上康复治疗。结果措施将在基线,4,12,24和52周获得;评估有效性为12周的主要端点。主要结果措施将是脚健康状况问卷(FHSQ)的脚疼痛领域。次要结果测量将包括FHSQ的功能域,第一个MTPJ疼痛的严重程度(使用100毫米的视觉模拟量表),症状的全局变化(使用15点李克特量表),健康状态(使用短窗体) -12®版本2.0和EUROQOL(EQ-5D-5L™)问卷),使用救援药物和共同干预,自我报告的不良事件和身体活动水平(使用偶然和计划的活动问卷)。将使用意向治疗原理进行分析数据。还将进行经济分析(成本效益和成本实用程序)。此外,使用三维运动分析系统和多通尺寸模型将在1周内检查干预措施的运动效应。讨论本研究将确定鞋加强插入件是否是用于缓解与第一MTPJ OA相关的疼痛的成本效益的干预。生物力学分析将提供有用的见解进入鞋加强插入件的作用机制。试验登记澳大利亚新西兰临床试验登记处,标识符:ACTRN12616000552482。 2016年4月28日注册。

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