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临床试验/NCT05232487
NCT05232487招募中不适用

Comparison of Swiss Versus Standard Low Back Acupuncture in Patients With Chronic Low Back Pain. A Randomized, Controlled, Single-blind, Monocentric Clinical Study

Li Yiming1 个研究点 分布在 1 个国家目标入组 116 人开始时间: 2023年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
116
试验地点
1
主要终点
Pain Severeity rated by 11-Point Numerical Rating Scale

研究概览

简要总结

Low back pain (LBP) is very common, widespread, and represents a multidimensional syndrome. It affects physical activity and function, health-related quality of life, and employment status. The lifetime prevalence of acute low back pain is approximately 80%. The prevalence of chronic low back pain (CLBP) in the general population is reported to be 8% to 21%. Several clinical trials have provided evidence to support the efficacy of acupuncture in the treatment of LBP, however, the optimal acupuncture treatment for CLBP has not been extensively studied.

详细描述

Low back pain (LBP) is a common, widespread and multifaceted syndrome and represents one of the leading sources of years lived with disability. In Switzerland, patients with LBP generated mean annual costs of 467 million Euro in 2016 and 2017, respectively. Moreover, quantity of prescriptions per patient was reported to be 5 - 6 per year, causing pain medication costs of 4.7 million Euro. It is estimated that 20% of acute LBP can manifest as chronic LBP (CLBP), defined as pain lasting longer than three months. CLBP does not only negatively impact the quality of life, functional status, and working capability of those suffering, but also plays a pivotal role of the large annual health care costs for LBP in Switzerland and worldwide. Pharmacological therapies with at least a small magnitude of effect for pain relief in CLBP include non-steroidal anti-inflammatory drugs, opioids, Tramadol and antidepressants. Additionally, non-pharmacological therapies with at least a small magnitude of effect for pain relief in CLBP include exercise, motor control exercise, Yoga, mindfulness-based stress reduction, electromyography biofeedback, cognitive-behavioral therapy, multidisciplinary rehabilitation and acupuncture.

In this context and during the last decades and centuries, different acupuncture methods evolved, among others, the acupuncture method newly termed "Swiss low back acupuncture" (SLBA). The SLBA originates from Jiu Gong Points (九宫穴), which is the abbreviation for "Nine Spinal Points" (脊椎九宫穴). The particular sites of Jiu Gong Points were evolved from the eight trigrams and nine palaces square (Ba Gua Jiu Gong fang 八卦九宫方). The eight trigrams (Ba Gua 八卦) are a set of metaphysical and philosophical sigmas composed of three components of yin and yang, which are the essential concept of all-natural phenomena. Nine palaces (Jiu Gong, 九宫), an element of the eight trigrams, correspond to the nine regions in ancient China (Jiu Ye, 九野). They represent the four main (North=kidney; South=heart; East=liver; West=lung; Earth=spleen) and four secondary cardinal points and the earth as the center. In 825 patients with LBP due to lumbar herniated disc, it has been shown that hot needle acupuncture (热针) using Jiu Gong Points around the most significant lesion of the lumbar vertebrae results in good improvements of pain. The uncontrolled study reported a cure of LBP in 65.2% of cases and an improvement of clinical symptoms of 32.4%. Due to the positive report, the hot needle acupuncture using Jiu Gong Points has further evolved in Switzerland and might be a promising tool to treat CLBP, since the optimal method of acupuncture against CLBP remains to be elucidated. However, the efficacy of SLBA has never been quantitatively compared to SA and a randomized clinical trial is warranted to provide first robust evidence on its performance in CLBP.

Therefore, the purpose of this study is to conduct the first randomized clinical trial comparing SLBA and SA on pain relief in patients with CLBP.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

盲法说明

Patients will be randomized by using the web-based secuTrial randomization tool and by applying an allocation ratio of 1:1 to SLBA and SA therapy. Patients and data analysts will be blinded to the intervention (SLBA or SA), however, acupuncturists performing the acupuncture sessions will not be blinded to the intervention.

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Female and male participants;
  • •Age between 18 and 75 years;
  • •Clinical diagnosis of CLBP with a disease duration of more than 3 months and an average pain intensity of minimally 4 points on a 11-point pain-numerical rating scale (pain-NRS) on the previous 7 days;
  • •Sufficient knowledge of German to complete the questionnaires.

排除标准

  • •All participants who do not meet the above-mentioned inclusion criteria;
  • •History or known severe concomitant diseases (e.g. abdominal aortic aneurysm, heart disease, cancer, psychiatric disorders).
  • •Other causes of low back pain not related to the clinical diagnosis of CLBP including inflammatory, malignant, or autoimmune disease;
  • •Planned or previous back surgery within 6 months
  • •Use of corticosteroids and/or other pain-relieving drugs that act through the central nervous system;
  • •Initiation of another therapy for CLBP within the last 4 weeks, e.g. physiotherapy;
  • •Preceding acupuncture treatment for CLBP during the past 6 months;
  • •Pregnancy;
  • •Participation in another clinical trial.

研究组 & 干预措施

Swiss low back acupuncture group

Experimental

Participants in this group will be treated with the Swiss low back acupuncture method.

干预措施: Swiss low back acupuncture (SLBA) (Other)

Standard acupuncture group

Active Comparator

Participants in this group will be treated with the standard acupuncture method.

干预措施: Standard acupuncture (SA) (Other)

结局指标

主要结局

Pain Severeity rated by 11-Point Numerical Rating Scale

时间窗: Difference in change between 9 weeks of treatment with SLBA compared to SA therapy.

Pain severity will be assessed by the 11-point numerical rating scale, ranging from 0 "No pain" to 10 "maximal pain".

次要结局

  • Changes in biopsychosocial health and quality of life(Difference in change between 9 weeks of treatment with SLBA compared to SA therapy; after 3 and 6 months follow-up.)
  • Changes in symptomatic distress(Difference in change between 9 weeks of treatment with SLBA compared to SA therapy; after 3 and 6 months follow-up.)
  • Changes in functional status and disability(Difference in change between 9 weeks of treatment with SLBA compared to SA therapy; after 3 and 6 months follow-up.)
  • Multidimensional Pain Inventory (MPI) - pain severity score(Difference in change between 9 weeks of treatment with SLBA compared to SA therapy.)
  • Pain diary(During the 9 weeks of treatment with SLBA compared to SA therapy.)

研究者

发起方
Li Yiming
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Li Yiming

Yiming Li, Prof. Dr. TCM univ. (CN) Dr. med.

TCM Ming Dao

研究点 (1)

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