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Chiropractic spinal manipulative therapy for migraine: a study protocol of a single-blinded placebo-controlled randomised clinical trial

机译:偏头痛的脊柱脊柱手法治疗:单盲安慰剂对照随机临床试验的研究方案

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Introduction Migraine affects 15% of the population, and has substantial health and socioeconomic costs. Pharmacological management is first-line treatment. However, acute and/or prophylactic medicine might not be tolerated due to side effects or contraindications. Thus, we aim to assess the efficacy of chiropractic spinal manipulative therapy (CSMT) for migraineurs in a single-blinded placebo-controlled randomised clinical trial (RCT). Method and analysis According to the power calculations, 90 participants are needed in the RCT. Participants will be randomised 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 the intervention and 3, 6 and 12?months. The primary end point is migraine frequency, while migraine duration, migraine intensity, headache index (frequency x duration x intensity) and medicine consumption are secondary end points. Primary analysis will assess a change in migraine frequency from baseline to the end of the intervention and follow-up, where the groups CSMT and placebo and CSMT and control will be compared. Owing to two group comparisons, p values below 0.025 will be considered statistically significant. For all secondary end points and analyses, a p value below 0.05 will be used. The results will be presented with the corresponding p values and 95% CIs. Ethics and dissemination The RCT will follow the clinical trial guidelines from the International Headache Society. The Norwegian Regional Committee for Medical Research Ethics and the Norwegian Social Science Data Services have approved the project. Procedure will be conducted according to the declaration of Helsinki. The results will be published at scientific meetings and in peer-reviewed journals. Trial registration number NCT01741714.
机译:简介偏头痛影响15%的人口,并带来大量的健康和社会经济成本。药理管理是一线治疗。但是,由于副作用或禁忌症,可能无法耐受急性和/或预防性药物。因此,我们旨在评估单盲安慰剂对照随机临床试验(RCT)中脊椎推拿手法治疗偏头痛的疗效。方法和分析根据能力计算,RCT需要90名参与者。参与者将被随机分为以下三类之一: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个月的干预以及干预结束时以及3个月,6个月和12个月的随访分析。主要终点是偏头痛发生频率,而偏头痛持续时间,偏头痛强度,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和随访结束时偏头痛频率的变化,将比较CSMT和安慰剂组以及CSMT和对照组。由于两组比较,低于0.025的p值将被认为具有统计学意义。对于所有次级终点和分析,将使用低于0.05的p值。结果将与相应的p值和95%CI一起显示。道德与传播RCT将遵循国际头痛协会的临床试验指南。挪威医学研究伦理区域委员会和挪威社会科学数据服务已批准该项目。程序将根据赫尔辛基的声明进行。结果将在科学会议和同行评审期刊上发表。试用注册号NCT01741714。

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