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多中心、开放标签、随机对照试验评估电针治疗手足冷过敏疗效与安全性的研究方案

Study Protocol for Multi-Center, Open-Label, Randomized Controlled Trial for Assessing the Efficacy and Safety of Electroacupuncture for Cold Hypersensitivity in Hands and Feet.

作者信息

Lee Kyou-Young, Lee Dong-Nyung, Kwon Na-Yoen, Kim Dong-Il, Yu Jun-Sang, Sun Seung-Ho

机构信息

Department of Ophthalmology, Otolaryngology, Dermatology, College of Korean Medicine, Sangji University, Wonju, Republic of Korea.

DongNam Esoo Korean Medicine Clinic, Cheongju, Republic of Korea.

出版信息

J Pharmacopuncture. 2025 Mar 31;28(1):47-56. doi: 10.3831/KPI.2025.28.1.47.

Abstract

OBJECTIVES

Cold hypersensitivity in the hands and feet (CHHF) is defined as the symptom of a sensation of coldness in the extremities under conditions that are not considered cold by an unaffected person. CHHF can affect the quality of life by placing restrictions on one's daily activities. Although electroacupuncture (EA) and acupuncture have been widely used for treating CHHF, randomized clinical trial (RCT) has not yet been conducted for evaluating the safety and efficacy of EA or acupuncture for the treatment of CHHF. This study aims to evaluate the effects of EA in CHHF patients.

METHODS

This study is a randomized, multicenter, and parallel design clinical trial. Overall, 72 participants will be randomly assigned to the EA treatment group, acupuncture treatment group, and untreated control group in 111 ratio via a web-based randomization system. The EA treatment group and acupuncture treatment group will receive EA or acupuncture treatment by visiting ten times at intervals of twice a week for five weeks. Follow-up visits will be made four weeks after the end of treatment. For the untreated control group, three visits will be made. The primary outcome measures will be the CHHF visual analogue scale score. Secondary outcome measures will be the body temperature of hands and feet, total scores of the Korean version of the World Health Organization Quality of Life Scale abbreviated version, the results of the questionnaire of health-related quality of life, questionnaire of demonstration, and questionnaire of cold hypersensitivity.

CONCLUSION

This study will be the first clinical trial to evaluate the efficacy and safety of EA for the treatment of CHHF. We expect this study to provide basic evidence for the treatment of CHHF with EA and future large-scale RCTs.

摘要

目的

手足冷过敏(CHHF)被定义为在未受影响的人不认为寒冷的条件下,四肢出现寒冷感的症状。CHHF会通过限制日常活动来影响生活质量。尽管电针(EA)和针灸已被广泛用于治疗CHHF,但尚未进行随机临床试验(RCT)来评估EA或针灸治疗CHHF的安全性和有效性。本研究旨在评估EA对CHHF患者的影响。

方法

本研究是一项随机、多中心、平行设计的临床试验。总体而言,72名参与者将通过基于网络的随机系统以1:1:1的比例随机分配到EA治疗组、针灸治疗组和未治疗对照组。EA治疗组和针灸治疗组将通过每周两次、为期五周的十次就诊接受EA或针灸治疗。治疗结束四周后进行随访。对于未治疗对照组,将进行三次就诊。主要结局指标将是CHHF视觉模拟量表评分。次要结局指标将是手足体温、世界卫生组织生活质量量表简版韩文版总分、健康相关生活质量问卷结果、示范问卷和冷过敏问卷。

结论

本研究将是第一项评估EA治疗CHHF有效性和安全性的临床试验。我们期望本研究为EA治疗CHHF及未来大规模RCT提供基础证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba91/11933916/cb36ee1cc637/jop-28-1-47-f1.jpg

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