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针刺干预颈椎病引起的颈痛的有效性:一项随机对照试验的研究方案。

Effectiveness of acupuncture intervention for neck pain caused by cervical spondylosis: study protocol for a randomized controlled trial.

机构信息

Affiliated Rehabilitation Hospital, Fujian University of Chinese Medicine, Fuzhou 350002, China.

出版信息

Trials. 2013 Jun 22;14:186. doi: 10.1186/1745-6215-14-186.

Abstract

BACKGROUND

Neck pain caused by cervical spondylosis has become a common health problem worldwide among >40-year-old adults. Acupuncture intervention is one of the most popular treatment measures for this disorder. However, evidence for its efficacy in relieving neck pain and recovering neck physiological function has not been established in randomized, placebo-controlled trials. The primary aim of this trial is to assess the efficacy and safety of active acupuncture compared with sham acupuncture intervention for neck pain caused by cervical spondylosis.

METHODS/DESIGN: We will conduct a randomized, double-blind, parallel-group, placebo-controlled trial comparing active acupuncture with placebo (sham acupuncture). A total of 456 patients with neck pain caused by cervical spondylosis who meet the eligibility criteria from outpatient clinics of the Second People's Hospital of Fujian Province and the Affiliated Rehabilitation Hospital, Fujian University of Traditional Chinese Medicine will be recruited and randomized into an active acupuncture or sham acupuncture group. The participants will undergo treatment sessions with either active or sham acupuncture intervention five times a week for 2 weeks. Evaluation by blinded assessors at baseline and at intervention for 1 and 2 weeks will include demographic characteristics, validated questionnaires (Northwick Park Neck Pain Questionnaire (NPQ) scale, Short-Form 36 (SF-36) scale, and McGill pain scale), examination of neck physiological function, and adverse events. All included patients will be followed up and investigated for relapse of neck pain at 4, 8, and 12 weeks after intervention.

DISCUSSION

This paper describes the rationale and design of a randomized double-blind, placebo-controlled trial that aims to determine the efficacy and safety of acupuncture intervention for neck pain caused by cervical spondylosis. The primary outcomes are changes in the NPQ score and neck physiological function. Secondary outcome measures include quality of life, adverse events, and relapse of neck pain. If successful, this project will provide evidence of the efficacy and safety of acupuncture for neck pain caused by cervical spondylosis.

TRIAL REGISTRATION

Chinese Clinical Trial Registry: ChiCTR-TRC-12002206. Registration date: 11 May 2012.

摘要

背景

颈椎病引起的颈痛已成为全球 40 岁以上成年人常见的健康问题。针刺干预是治疗这种疾病最受欢迎的措施之一。然而,在随机、安慰剂对照试验中,并没有证据表明其缓解颈痛和恢复颈部生理功能的疗效。本试验的主要目的是评估与假针刺干预相比,主动针刺治疗颈椎病引起的颈痛的疗效和安全性。

方法/设计:我们将进行一项随机、双盲、平行组、安慰剂对照试验,比较主动针刺与安慰剂(假针刺)。共有 456 名符合福建省第二人民医院和福建中医药大学附属康复医院门诊标准的颈椎病颈痛患者将被招募并随机分为主动针刺组或假针刺组。参与者将接受每周 5 次的主动或假针刺干预治疗,持续 2 周。在基线和干预后 1 周和 2 周,由盲法评估者进行评估,包括人口统计学特征、验证性问卷(Northwick Park 颈痛问卷(NPQ)量表、SF-36 量表和麦吉尔疼痛量表)、颈部生理功能检查和不良事件。所有纳入的患者将在干预后 4、8 和 12 周进行随访和颈痛复发调查。

讨论

本文描述了一项随机双盲、安慰剂对照试验的原理和设计,旨在确定针刺干预颈椎病颈痛的疗效和安全性。主要结局指标是 NPQ 评分和颈部生理功能的变化。次要结局指标包括生活质量、不良事件和颈痛复发。如果成功,该项目将为针刺治疗颈椎病颈痛的疗效和安全性提供证据。

试验注册

中国临床试验注册中心:ChiCTR-TRC-12002206。注册日期:2012 年 5 月 11 日。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd8c/3700747/7b59aa042ee4/1745-6215-14-186-1.jpg

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