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首页> 外文期刊>Journal of Foot and Ankle Research >A protocol for a randomised controlled trial of prefabricated versus customised foot orthoses for people with rheumatoid arthritis: the FOCOS RA trial [Foot Orthoses – Customised v Off-the-Shelf in Rheumatoid Arthritis]
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A protocol for a randomised controlled trial of prefabricated versus customised foot orthoses for people with rheumatoid arthritis: the FOCOS RA trial [Foot Orthoses – Customised v Off-the-Shelf in Rheumatoid Arthritis]

机译:用于预制对照试验的方案对类风湿性关节炎的人的预制与定制脚矫正尺寸:FOCOS RA试验[脚矫形器 - 风湿性关节炎的自定义V现成]

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摘要

Foot pain is common in rheumatoid arthritis and appears to persist despite modern day medical management. Several clinical practice guidelines currently recommend the use of foot orthoses for the treatment of foot pain in people with rheumatoid arthritis. However, an evidence gap currently exists concerning the comparative clinical- and cost-effectiveness of prefabricated and customised foot orthoses in people with early rheumatoid arthritis. Early intervention with orthotics may offer the best opportunity for positive therapeutic outcomes. The primary aim of this study is to evaluate the comparative clinical- and cost-effectiveness of prefabricated versus customised orthoses for reducing foot pain over 12?months. This is a multi-centre two-arm parallel randomised controlled trial comparing prefabricated versus customised orthoses in participants with early rheumatoid arthritis (?2?years disease duration). A total of 160 (a minimum of 80 randomised to each arm) eligible participants will be recruited from United Kingdom National Health Service Rheumatology Outpatient Clinics. The primary outcome will be foot pain measured via the Foot Function Index pain subscale at 12?months. Secondary outcomes will include foot related impairments and disability via the Foot Impact Scale for rheumatoid arthritis, global functional status via the Stanford Health Assessment Questionnaire, foot disease activity via the Rheumatoid Arthritis Foot Disease Activity Index, and health-related quality of life at baseline, 6 and 12?months. Process outcomes will include recruitment/retention rates, data completion rates, intervention adherence rates, and participant intervention and trial participation satisfaction. Cost-utility and cost-effectiveness analyses will be undertaken. Outcome measures collected at baseline, 6 and 12?months will be used to evaluate the comparative clinical- and cost- effectiveness of customised versus prefabricated orthoses for this treatment of early rheumatoid arthritis foot conditions. This trial will help to guide orthotic prescription recommendations for the management of foot pain for people with early rheumatoid arthritis in future. ISRCTN13654421. Registered 09 February 2016.
机译:脚疼痛在类风湿性关节炎中常见,尽管现代医疗管理似乎持续存在。几个临床实践指南目前建议使用脚部偏离的患者对类风湿性关节炎的人们的脚疼痛。然而,目前有关于具有早期类风湿性关节炎的预制和定制脚垂直术的比较临床和成本效益的证据差距。利用矫反神性的早期干预可能为正疗法结果提供最佳机会。本研究的主要目的是评估预制与定制裸装的比较临床和成本效益,以减少12个月的脚疼痛。这是一个多中心双臂并联随机对照试验比较预制与早期类风湿性关节炎的参与者的定制矫形器(<?2?年疾病持续时间)。总共160名(至少80名随机为每只武器)符合条件的参与者将从英国国家卫生服务风湿病门诊诊所招募。主要结果将是通过脚函数指数疼痛子围击测量的足够疼痛,在12?几个月。二次结果将通过脚部冲击量表,通过斯坦福健康评估问卷,通过类风湿性关节炎足疾病活动指数,基线与健康相关生活质量,通过斯坦福卫生性关节炎,全球功能状况,全球功能状况。 6和12?几个月。过程结果将包括招聘/保留率,数据完成率,干预遵守率以及参与者干预和试验参与满意度。将进行成本实用性和成本效益分析。在基线,6和12月收集的结果措施将用于评估定制与预制旁矫正术的比较临床和成本效果,用于该治疗早期类风湿性关节炎足部条件。本次审判将有助于指导矫形处方建议,以便将来为早期类风湿性关节炎的人们进行脚痛的管理。 ISRCTN13654421。注册2016年2月9日。

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