首页> 外文OA文献 >Efficacy of manual therapy treatments for people with cervicogenic dizziness and pain: protocol of a randomised controlled trial
【2h】

Efficacy of manual therapy treatments for people with cervicogenic dizziness and pain: protocol of a randomised controlled trial

机译:手动疗法对宫颈源性头晕和疼痛患者的疗效:一项随机对照试验的方案

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Background: Cervicogenic dizziness is a disabling condition characterised by postural unsteadiness that is aggravated by cervical spine movements and associated with a painful and/or stiff neck. Two manual therapy treatments (Mulligan’s Sustained Natural Apophyseal Glides (SNAGs) and Maitland’s passive joint mobilisations) are used by physiotherapists to treat this condition but there is little evidence from randomised controlled trials to support their use. The aim of this study is to conduct a randomised controlled trial to compare these two forms of manual therapy (Mulligan glides and Maitland mobilisations) to each other and to a placebo in reducing symptoms of cervicogenic dizziness in the longer term and to conduct an economic evaluation of the interventions. Methods: Participants with symptoms of dizziness described as imbalance, together with a painful and/or stiff neck will be recruited via media releases, advertisements and mail-outs to medical practitioners in the Hunter region of NSW, Australia. Potential participants will be screened by a physiotherapist and a neurologist to rule out other causes of their dizziness. Once diagnosed with cervciogenic dizziness, 90 participants will be randomly allocated to one of three groups: Maitland mobilisations plus range-of-motion exercises, Mulligan SNAGs plus self-SNAG exercises or placebo. Participants will receive two to six treatments over six weeks. The trial will have unblinded treatment but blinded outcome assessments. Assessments will occur at baseline, post-treatment, six weeks, 12 weeks, six months and 12 months post treatment. The primary outcome will be intensity of dizziness. Other outcome measures will be frequency of dizziness, disability, intensity of cervical pain, cervical range of motion, balance, head repositioning, adverse effects and treatment satisfaction. Economic outcomes will also be collected. Discussion: This paper describes the methods for a randomised controlled trial to evaluate the effectiveness of two manual therapy techniques in the treatment of people with cervicogenic dizziness for which there is limited established evidence-based treatment.
机译:背景:颈源性头晕是一种致残性疾病,其特征是姿势不稳,颈椎运动加剧,并伴有颈部疼痛和/或僵硬。理疗师使用了两种手动疗法(Mulligan的天然天然骨phy滑行药(SNAG)和Maitland的被动关节动员法)来治疗这种情况,但随机对照试验几乎没有证据支持这种疗法。这项研究的目的是进行一项随机对照试验,以比较这两种形式的手动疗法(Mulligan滑行疗法和梅特兰动员疗法)以及安慰剂,以长期减轻宫颈源性头晕的症状并进行经济评估的干预措施。方法:通过媒体发布,广告和邮寄的方式向澳大利亚新南威尔士州亨特地区的医务人员招募头晕症状为失衡,颈部疼痛和/或僵硬的参与者。物理治疗师和神经科医生将筛选潜在的参与者,以排除引起头昏眼花的其他原因。一旦被诊断出患有宫颈源性头晕,则将90名参与者随机分配到以下三个组之一:梅特兰动员加运动范围练习,Mulligan SNAG加自体SNAG练习或安慰剂。参与者将在六周内接受两到六次治疗。该试验将采用无盲法治疗,但盲目评估结局。评估将在治疗后的基线,治疗后,六周,十二周,六个月和十二个月进行。主要结果将是头晕的强度。其他结局指标包括头晕频率,残疾,宫颈疼痛程度,宫颈活动范围,平衡,头部重新定位,不良反应和治疗满意度。经济成果也将被收集。讨论:本文介绍了一项随机对照试验的方法,以评估两种人工疗法在治疗宫颈源性头晕的患者中的有效性,这些患者的既有证据基础有限。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号