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一项针对近期发病、伴有疼痛的神经根型颈椎病的多模式物理治疗与建议的随机对照试验——PACeR 试验方案。

A randomised controlled trial of multimodal physiotherapy versus advice for recent onset, painful cervical radiculopathy - the PACeR trial protocol.

机构信息

School of Physiotherapy, Royal College of Surgeons in Ireland (RCSI), Dublin, Ireland.

Department of Physiotherapy, Beaumont Hospital, Dublin, Ireland.

出版信息

BMC Musculoskelet Disord. 2019 Jun 1;20(1):265. doi: 10.1186/s12891-019-2639-4.

Abstract

BACKGROUND

A research gap exists for optimal management of cervical radiculopathy in the first 12 weeks and short term natural history of the condition is somewhat unclear, although thought to be favourable. The primary aim of this assessor blinded, superiority, 2 parallel group randomised controlled trial is to investigate the effects of a 4 week physiotherapy programme (6-8 sessions) of manual therapy, exercise and upper limb neural unloading tape, compared to a control of weekly phone advice; on disability, pain and selected biopsychosocial measures, in acute and sub-acute cervical radiculopathy patients. A secondary aim is to identify whether any baseline variables, symptom duration or group allocation can predict outcome.

METHODS

Participants are recruited from GP referrals in an urban setting, from a neurosurgery non-urgent waiting list and from self-referral through Facebook advertising. Eligible participants (n = 64) are diagnosed with radiculopathy based on a clinical prediction rule and must have symptoms of unilateral, single level, radiculopathy for between 2 and 12 weeks, without having yet received physiotherapy. Random 1:1 group allocation (using variable block sizes), allocation concealment, blinded assessment and intention to treat analysis are being employed. Treatment is provided by clinical specialist physiotherapists in primary and secondary care settings. Outcomes are measured at baseline, 4 (primary endpoint) and 12 weeks. Participants' report of pain, disability and their rating of recovery is also recorded by telephone interview at 6 months. Statistical analysis of between group differences will be performed with ANOVAs and MANOVAs, and multivariable regression analysis will be undertaken to explore predictor variables. Ethical approval for this study has been received from the Beaumont Hospital and Irish College of General Practitioners Research Ethics Committees. The trial is registered at ClinicalTrials.gov (NCT02449200).

DISCUSSION

An internal pilot study to test retention and recruitment strategies led to trial expansion and this is now a multi centre trial involving 5 clinical sites.

TRIAL REGISTRATION

NCT02449200 . Registered 20/05/15.

摘要

背景

在最初的 12 周内,颈椎神经根病的最佳治疗方法存在研究空白,并且该疾病的短期自然病程尚不清楚,尽管人们认为其病程是有利的。本项评估员设盲、优效性、2 项平行组随机对照试验的主要目的是,调查为期 4 周的物理治疗方案(6-8 次治疗)的疗效,该方案包括手法治疗、运动和上肢神经减压贴,与每周电话咨询的对照组相比,该方案在急性和亚急性颈椎神经根病患者的残疾、疼痛和选定的生物心理社会测量指标方面的效果。次要目的是确定任何基线变量、症状持续时间或组分配是否可以预测结局。

方法

参与者是从城市环境中的全科医生转诊、神经外科非紧急候诊名单和通过 Facebook 广告的自我转诊中招募的。符合条件的参与者(n=64)根据临床预测规则诊断为神经根病,且必须出现单侧、单节段神经根病的症状 2 至 12 周,且尚未接受过物理治疗。采用 1:1 随机分组(使用可变大小的区组)、分配隐藏、盲法评估和意向治疗分析。治疗由初级和二级保健环境中的临床专科物理治疗师提供。在基线、4 周(主要终点)和 12 周时测量结局。参与者通过电话访谈报告疼痛、残疾和他们对恢复的评分,在 6 个月时也进行记录。采用方差分析和多元方差分析对组间差异进行统计学分析,并采用多变量回归分析来探索预测变量。本研究已获得 Beaumont 医院和爱尔兰全科医生学院研究伦理委员会的伦理批准。该试验已在 ClinicalTrials.gov(NCT02449200)注册。

讨论

一项内部试点研究测试了保留和招募策略,导致试验扩大,现在这是一项涉及 5 个临床站点的多中心试验。

试验注册

NCT02449200。注册于 2015 年 5 月 20 日。

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