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Chiropractic spinal manipulative therapy for cervicogenic headache: a study protocol of a single-blinded placebo-controlled randomized clinical trial

机译:脊椎推拿手法治疗宫颈源性头痛:单盲安慰剂对照随机临床试验的研究方案

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摘要

Cervicogenic headache (CEH) is a secondary headache which affects 1.0–4.6 % of the population. Although the costs are unknown, the health consequences are substantial for the individual; especially considering that they often suffers chronicity. Pharmacological management has no or only minor effect on CEH. Thus, we aim to assess the efficacy of chiropractic spinal manipulative therapy (CSMT) for CEH in a single-blinded placebo-controlled randomized clinical trial (RCT). According to the power calculations, we aim to recruit 120 participants to the RCT. Participants will be randomized into one of three groups; CSMT, placebo (sham manipulation) and control (usual non-manual management). The RCT consists of three stages: 1 month run-in, 3 months intervention and follow-up analyses at the end of intervention and 3, 6 and 12 months. Primary end-point is headache frequency, while headache duration, headache intensity, headache index (frequency × duration × intensity) and medicine consumption are secondary end-points. Primary analysis will assess a change in headache frequency from baseline to the end of intervention and to follow-up, where the groups CSMT and placebo and CSMT and control will be compared. Due to two group-comparisons, the results with p values below 0.025 will be considered statistically significant. For all secondary end-points and analyses, the significance level of 0.05 will be used. The results will be presented with the corresponding p values and 95 % confidence intervals. To our knowledge, this is the first prospective manual therapy three-armed single-blinded placebo-controlled RCT to be conducted for CEH. Current RCTs suggest efficacy in headache frequency, duration and intensity. However a firm conclusion requires clinical single-blinded placebo-controlled RCTs with few methodological shortcomings. The present study design adheres to the recommendations for pharmacological RCTs as far as possible and follows the recommended clinical trial guidelines by the International Headache Society.Trial registration ClinicalTrials.gov identifier: , 2 December 2012
机译:颈源性头痛(CEH)是继发性头痛,影响1.0-4.6%的人口。尽管费用未知,但对个人的健康后果是巨大的。特别是考虑到他们经常患有慢性病。药理管理对CEH没有影响或仅有很小的影响。因此,我们的目的是在单盲安慰剂对照随机临床试验(RCT)中评估脊椎推拿手法治疗CEH的疗效。根据能力计算,我们旨在招募120名RCT参与者。参加者将被随机分为三组之一; CSMT,安慰剂(假手术)和对照(通常为非人工管理)。 RCT包括三个阶段:1个月的磨合,3个月的干预和干预结束时以及3、6和12个月的随访分析。主要终点是头痛频率,而头痛持续时间,头痛强度,头痛指数(频率×持续时间×强度)和药物消耗是次要终点。初步分析将评估从基线到干预结束以及随访期间头痛频率的变化,在此将对CSMT和安慰剂组以及CSMT和对照组进行比较。由于进行了两次组比较,p值低于0.025的结果将被认为具有统计学意义。对于所有次要终点和分析,将使用显着性水平0.05。结果将与相应的p值和95%置信区间一起显示。据我们所知,这是首次针对CEH进行的前瞻性手动疗法三臂单盲安慰剂对照RCT。当前的RCT显示出对头痛频率,持续时间和强度的功效。然而,有力的结论需要临床单盲安慰剂对照的RCT,方法学上的缺陷很少。本研究设计尽可能遵守针对药理学RCT的建议,并遵循国际头痛协会的推荐临床试验指南。试验注册ClinicalTrials.gov标识符:2012年12月2日

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