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定制与现货踝足矫形器治疗脑卒中患者的随机对照试验

Bespoke versus off-the-shelf ankle-foot orthosis for people with stroke: randomized controlled trial.

机构信息

1 Stroke Research Centre, University of Manchester and Manchester Academic Health Science Centre, Manchester, UK.

2 Division of Nursing, Midwifery and Social Work, University of Manchester and Manchester Academic Health Science Centre, Manchester, UK.

出版信息

Clin Rehabil. 2018 Mar;32(3):367-376. doi: 10.1177/0269215517728764. Epub 2017 Aug 31.

Abstract

OBJECTIVE

The aim of the study was to compare the effect of two designs of ankle-foot orthosis on people with stroke.

DESIGN

The study design was an assessor-blind, multicentre randomized controlled trial.

SETTING

The setting was community stroke services.

PARTICIPANTS

A total of 139 community-dwelling stroke survivors with limited mobility were recruited.

INTERVENTIONS

The two most commonly used types of ankle-foot orthosis (bespoke and off-the-shelf) were chosen.

MAIN MEASURES

The main measures of the study were as follows: short- (6 weeks) and long-term (12 weeks) effects on stroke survivors' satisfaction; adverse events; mobility (Walking Handicap Scale); fear of falling (Falls Efficacy Scale-International (FES-I)) and walking impairments (gait speed and step length using the 5-m walk test).

RESULTS

Long-term satisfaction was non-significantly higher in the off-the-shelf group: 72% versus 64%; OR (95% CI) = 0.64 (0.31 to 1.3); P = 0.21. No statistically significant differences were found between the orthoses except that the off-the-shelf group had less fear of falling at short-term follow-up than the bespoke group: mean difference (95% CI) = -4.6 (-7.6 to -1.6) points on the FES-I; P = 0.003.

CONCLUSION

No differences between off-the-shelf and bespoke ankle-foot orthoses were found except that participants in the off-the-shelf orthosis group had less fear of falling at short-term follow-up.

摘要

目的

本研究旨在比较两种踝足矫形器设计对脑卒中患者的影响。

设计

研究设计为评估者盲、多中心随机对照试验。

设置

设置为社区脑卒中服务。

参与者

共招募了 139 名行动不便的社区居住脑卒中幸存者。

干预措施

选择了两种最常用的踝足矫形器(定制和现成)。

主要措施

本研究的主要措施如下:短期(6 周)和长期(12 周)对脑卒中幸存者满意度的影响;不良事件;移动性(步行障碍量表);跌倒恐惧(跌倒效能量表-国际版(FES-I))和步行障碍(5 米步行测试的步速和步长)。

结果

现成组的长期满意度显著较高:72%对 64%;OR(95%CI)=0.64(0.31 至 1.3);P=0.21。两种矫形器之间没有统计学上的显著差异,除了在短期随访时现成组的跌倒恐惧程度低于定制组:FES-I 平均差值(95%CI)=-4.6(-7.6 至-1.6)点;P=0.003。

结论

除了在短期随访时现成组的跌倒恐惧程度较低外,现成和定制踝足矫形器之间没有发现差异。

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