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一项单盲、随机、平行组优势试验,旨在研究鞋类和定制足部矫形器与仅使用鞋类相比,对髌股关节骨关节炎患者的影响:一项II期试点试验方案。

A single-blinded, randomized, parallel group superiority trial investigating the effects of footwear and custom foot orthoses versus footwear alone in individuals with patellofemoral joint osteoarthritis: a phase II pilot trial protocol.

作者信息

Wyndow Narelle, Crossley Kay M, Vicenzino Bill, Tucker Kylie, Collins Natalie J

机构信息

School of Health and Rehabilitation Sciences, The University of Queensland, St Lucia, 4072 QLD Australia.

School of Allied Health, College of Science, Health and Engineering, La Trobe University, Bundoora, 3086 VIC Australia.

出版信息

J Foot Ankle Res. 2017 Apr 26;10:19. doi: 10.1186/s13047-017-0200-y. eCollection 2017.

Abstract

BACKGROUND

Patellofemoral joint osteoarthritis is a common condition, yet information regarding conservative management is lacking. Foot orthoses are an effective intervention for improving pain and function in younger individuals with patellofemoral pain and may be effective in those with patellofemoral osteoarthritis. This pilot study will seek to establish the feasibility of a phase III randomised controlled trial to investigate whether foot orthoses worn in prescribed motion controlled footwear are superior to prescribed motion control footwear alone in the management of patellofemoral osteoarthritis.

METHODS/DESIGN: This phase II pilot clinical trial is designed as a randomized, single-blind, parallel group, two arm, superiority trial. The trial will recruit 44 participants from Queensland and Tasmania, Australia. Volunteers aged 40 years and over must have clinical symptoms and radiographic evidence of patellofemoral osteoarthritis to be eligible for inclusion. Those eligible will be randomized to receive either foot orthoses and prescribed motion control shoes, or prescribed motion control shoes alone, to be worn for a period of 4 months. The feasibility of a phase III clinical trial will be evaluated by assessing factors such as recruitment rate, number of eligible participants, participant compliance with the study protocol, adverse events, and drop-out rate. A secondary aim of the study will be to determine completion rates and calculate effect sizes for patient reported outcome measures such as knee-related symptoms, function, quality of life, kinesiophobia, self-efficacy, general and mental health, and physical activity at 2 and 4 months. Primary outcomes will be reported descriptively while effect sizes and 95% confidence intervals will be calculated for the secondary outcome measures. Data will be analysed using an intention-to-treat principle.

DISCUSSION

The results of this pilot trial will help determine the feasibility of a phase III clinical trial investigating whether foot orthoses plus motion control footwear are superior to motion control footwear alone in individuals with patellofemoral osteoarthritis. A Phase III clinical trial will help guide footwear and foot orthoses recommendations in the clinical management of this disorder.

TRIAL REGISTRATION

Retrospectively registered with the Australian New Zealand Clinical Trials Registry: ACTRN12615000002583. Date registered: 07/01/15.

摘要

背景

髌股关节骨关节炎是一种常见病症,但关于保守治疗的信息却很匮乏。足部矫形器对于改善患有髌股疼痛的年轻个体的疼痛和功能是一种有效的干预措施,并且可能对患有髌股关节骨关节炎的患者也有效。这项试点研究旨在确定一项III期随机对照试验的可行性,以调查在髌股关节骨关节炎的治疗中,在规定的运动控制鞋类中佩戴足部矫形器是否优于单独使用规定的运动控制鞋类。

方法/设计:这项II期试点临床试验设计为一项随机、单盲、平行组、双臂优效性试验。该试验将从澳大利亚昆士兰州和塔斯马尼亚州招募44名参与者。年龄在40岁及以上的志愿者必须有髌股关节骨关节炎的临床症状和影像学证据才有资格被纳入。符合条件的参与者将被随机分配接受足部矫形器和规定的运动控制鞋,或仅接受规定的运动控制鞋,佩戴4个月。III期临床试验的可行性将通过评估招募率、符合条件的参与者数量、参与者对研究方案的依从性、不良事件和脱落率等因素来评估。该研究的次要目的将是确定完成率,并计算患者报告的结局指标的效应大小,如膝关节相关症状、功能、生活质量、运动恐惧、自我效能、总体和心理健康以及2个月和4个月时的身体活动情况。主要结局将进行描述性报告,而效应大小和95%置信区间将针对次要结局指标进行计算。数据将采用意向性分析原则进行分析。

讨论

这项试点试验的结果将有助于确定一项III期临床试验的可行性,该试验旨在研究在患有髌股关节骨关节炎的个体中,足部矫形器加运动控制鞋类是否优于单独的运动控制鞋类。一项III期临床试验将有助于指导在这种疾病的临床管理中关于鞋类和足部矫形器的建议。

试验注册

追溯注册于澳大利亚新西兰临床试验注册中心:ACTRN12615000002583。注册日期:2015年1月7日。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/beb0/5405497/281aee678d2a/13047_2017_200_Fig1_HTML.jpg

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