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小脑性共济失调康复研究:一项针对遗传性小脑性共济失调患者门诊和家庭支持性物理治疗方案的随机对照试验方案。

Rehabilitation for ataxia study: protocol for a randomised controlled trial of an outpatient and supported home-based physiotherapy programme for people with hereditary cerebellar ataxia.

机构信息

Bruce Lefroy Centre for Genetic Health Research, Murdoch Children's Research Institute, Parkville, Victoria, Australia.

Physiotherapy Department, Monash Health, Cheltenham, Victoria, Australia.

出版信息

BMJ Open. 2020 Dec 17;10(12):e040230. doi: 10.1136/bmjopen-2020-040230.

Abstract

INTRODUCTION

Emerging evidence indicates that rehabilitation can improve ataxia, mobility and independence in everyday activities in individuals with hereditary cerebellar ataxia. However, with the rarity of the genetic ataxias and known recruitment challenges in rehabilitation trials, most studies have been underpowered, non-randomised or non-controlled. This study will be the first, appropriately powered randomised controlled trial to examine the efficacy of an outpatient and home-based rehabilitation programme on improving motor function for individuals with hereditary cerebellar ataxia.

METHODS AND ANALYSIS

This randomised, single-blind, parallel group trial will compare a 30-week rehabilitation programme to standard care in individuals with hereditary cerebellar ataxia. Eighty individuals with a hereditary cerebellar ataxia, aged 15 years and above, will be recruited. The rehabilitation programme will include 6 weeks of outpatient land and aquatic physiotherapy followed immediately by a 24- week home exercise programme supported with fortnightly physiotherapy sessions. Participants in the standard care group will be asked to continue their usual physical activity. The primary outcome will be the motor domain of the Functional Independence Measure. Secondary outcomes will measure the motor impairment related to ataxia, balance, quality of life and cost-effectiveness. Outcomes will be administered at baseline, 7 weeks, 18 weeks and 30 weeks by a physiotherapist blinded to group allocation. A repeated measures mixed-effects linear regression model will be used to analyse the effect of the treatment group for each of the dependent continuous variables. The primary efficacy analysis will follow the intention-to-treat principle.

ETHICS AND DISSEMINATION

The study has been approved by the Monash Health Human Research Ethics Committee (HREC/18/MonH/418) and the Human Research Ethics Committee of the Northern Territory Department of Health and Menzies School of Health Research (2019/3503). Results will be published in peer-reviewed journals, presented at national and/or international conferences and disseminated to Australian ataxia support groups.

TRIAL REGISTRATION NUMBER

ACTRN12618000908235.

摘要

简介

新出现的证据表明,康复治疗可以改善遗传性小脑性共济失调患者的共济失调、移动能力和日常活动中的独立性。然而,由于遗传性共济失调的罕见性以及康复试验中已知的招募挑战,大多数研究的效力都不足,要么是非随机的,要么是非对照的。这项研究将是第一项适当效力的随机对照试验,旨在检验门诊和家庭为基础的康复方案对遗传性小脑性共济失调患者运动功能的疗效。

方法和分析

这是一项随机、单盲、平行组试验,将比较 30 周的康复方案与遗传性小脑性共济失调患者的标准护理。将招募 80 名年龄在 15 岁及以上的遗传性小脑性共济失调患者。康复方案将包括 6 周的门诊陆地和水上物理治疗,随后立即进行 24 周的家庭运动方案,并辅以每两周一次的物理治疗。标准护理组的参与者将被要求继续进行他们通常的体育活动。主要结果将是功能独立性测量的运动领域。次要结果将衡量与共济失调、平衡、生活质量和成本效益相关的运动障碍。由一名对分组分配不知情的物理治疗师在基线、7 周、18 周和 30 周进行评估。将使用重复测量混合效应线性回归模型分析治疗组对每个依赖连续变量的影响。主要疗效分析将遵循意向治疗原则。

伦理和传播

该研究已获得莫纳什健康人类研究伦理委员会(HREC/18/MonH/418)和北领地卫生部和梅宁斯健康研究学院人类研究伦理委员会(2019/3503)的批准。研究结果将发表在同行评议的期刊上,在国家和/或国际会议上展示,并传播给澳大利亚共济失调支持团体。

试验注册号

ACTRN12618000908235。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb80/7747606/48e8119d19cb/bmjopen-2020-040230f01.jpg

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