Gallagher Kellie S, Godwin Jon, Hendry Gordon J, Steultjens Martijn, Woodburn Jim
1University of East London, Stratford, Water Lane, London, England E15 4LZ UK.
2Glasgow Caledonian University, Institute for Applied Health Research, School of Health & Life Sciences, Cowcaddens Road, Glasgow, Scotland G4 0BA UK.
J Foot Ankle Res. 2018 May 31;11:24. doi: 10.1186/s13047-018-0272-3. eCollection 2018.
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.
METHODS/DESIGN: 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.
足痛在类风湿关节炎中很常见,尽管有现代医学治疗手段,但疼痛似乎仍会持续。目前有几项临床实践指南推荐使用足部矫形器来治疗类风湿关节炎患者的足痛。然而,对于早期类风湿关节炎患者,预制足部矫形器和定制足部矫形器在临床疗效和成本效益方面的比较,目前还存在证据空白。早期使用矫形器干预可能提供获得积极治疗效果的最佳机会。本研究的主要目的是评估预制矫形器与定制矫形器在12个月内减轻足痛方面的临床疗效和成本效益。
方法/设计:这是一项多中心双臂平行随机对照试验,比较早期类风湿关节炎(病程<2年)患者使用预制矫形器与定制矫形器的效果。将从英国国民健康服务体系的风湿病门诊招募总共160名符合条件的参与者(每组至少随机分配80名)。主要结局指标将是在12个月时通过足部功能指数疼痛子量表测量的足痛情况。次要结局指标将包括通过类风湿关节炎足部影响量表评估的与足部相关的功能障碍和残疾情况、通过斯坦福健康评估问卷评估的整体功能状态、通过类风湿关节炎足部疾病活动指数评估的足部疾病活动情况,以及在基线、6个月和12个月时的健康相关生活质量。过程指标将包括招募/留存率、数据完成率、干预依从率,以及参与者对干预措施和试验参与的满意度。将进行成本效用分析和成本效益分析。
在基线、6个月和12个月时收集的结局指标将用于评估定制矫形器与预制矫形器在治疗早期类风湿关节炎足部疾病方面的临床疗效和成本效益。该试验将有助于指导未来针对早期类风湿关节炎患者足痛管理的矫形器处方建议。
ISRCTN13654421。于2016年2月9日注册。