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The STAP-study: The (cost) effectiveness of custom made orthotic insoles in the treatment for plantar fasciopathy in general practice and sports medicine: Design of a randomized controlled trial

机译:STAP研究:定制的矫形鞋垫在一般实践和运动医学中治疗足底筋膜病的(成本)效果:一项随机对照试验的设计

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摘要

textabstractBackground: Plantar fasciopathy is a common cause of foot pain, accounting for 11 to 15 % of all foot symptoms requiring professional care in adults. Although many patients have complete resolution of symptoms within 12 months, many patients wish to reduce this period as much as possible. Orthotic devices are a frequently applied option of treatment in daily practice, despite a lack of evidence on the effectiveness. Therefore, the objective is to study the (cost)-effectiveness of custom made insoles by a podiatrist, compared to placebo insoles and usual care in patients with plantar fasciopathy in general practice and sports medicine clinics. Method/design: This study is a multi-center three-armed participant and assessor-blinded randomized controlled trial with 6-months follow-up. Patients with plantar fasciopathy, with a minimum duration of complaints of 2 weeks and aged between 18 and 65, who visit their general practitioner or sport physician are eligible for inclusion. A total of 185 patients will be randomized into three parallel groups. One group will receive usual care by the general practitioner or sports physician alone, one group will be referred to a podiatrist and will receive a custom made insole, and one group will be referred to a podiatrist and will receive a placebo insole. The primary outcome will be the change from baseline to 12 weeks follow-up in pain severity at rest and during activity on a 0-10 numerical rating scale (NRS). Secondary outcomes include foot function (according to the Foot Function Index) at 6, 12 and 26 weeks, recovery (7-point Likert) at 6, 12 and 26 weeks, pain at rest and during activity (NRS) at 6 and 26 weeks and cost-effectiveness of the intervention at 26-weeks. Measurements will take place at baseline and at, 2, 4, 6, 12 and 26 weeks of follow-up. Discussion: The treatment of plantar fasciopathy is a challenge for health care professionals. Orthotic devices are frequently applied, despite a lack of evidence of the effectiveness on patient reported outcome. The results of this randomized controlled trial will improve the evidence base for treating this troublesome condition in daily practice. Trial registration: Dutch Trial Registration: NTR5346. Date of registration: August 5th 2015.
机译:足底筋膜病是足部疼痛的常见原因,占成年人需要专业护理的所有脚部症状的11%至15%。尽管许多患者在12个月内症状已完全缓解,但许多患者希望尽可能缩短这一时间段。尽管缺乏有效的证据,矫形装置还是日常实践中经常使用的治疗方法。因此,目的是研究足底筋膜病患者在一般实践和运动医学诊所中,与安慰剂鞋垫和常规护理相比,足病医生定制的鞋垫的(成本)效果。方法/设计:本研究是一项多中心三臂参与者和评估者盲目的随机对照试验,随访6个月。足底筋膜病患者的病程最少为2周,且年龄在18至65岁之间,他们会拜访他们的全科医生或运动医生,才有资格纳入研究。总共185名患者将被随机分为三个平行组。一组将由全科医生或运动医师单独接受常规护理,一组将被称为足病医生,将接受定制的鞋垫,一组将被称为足病医生,并接受安慰剂的鞋垫。主要结果将是从基线到12周的随访(休息和活动期间疼痛严重程度以0-10数字评分表(NRS)进行的变化)。次要结果包括第6、12和26周的足功能(根据Foot功能指数),第6、12和26周的恢复(7点Likert),第6和26周的休息和运动中疼痛(NRS)在26周时的干预措施的成本效益。测量将在基线以及随访的第2、4、6、12和26周进行。讨论:足底筋膜病的治疗对卫生保健专业人员构成挑战。尽管缺乏对患者报告的结局有效的证据,但还是经常使用矫形器。这项随机对照试验的结果将改善日常实践中治疗这种麻烦病症的证据基础。试用注册:荷兰试用注册:NTR5346。注册日期:2015年8月5日。

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