Effect of acupuncture with donepezil based on syndrome differentiation on cognitive function in patients with mild-to-moderate Alzheimer's disease: a study protocol for a multicenter randomized controlled trial

被引:0
|
作者
Fu, Qin-Hui [1 ]
Pei, Jian [1 ]
Zhou, Hou-guang [2 ]
Wang, Tao [3 ]
Zhan, Yi-jun [1 ]
Tao, Lin [1 ]
Xu, Jia [1 ]
Zhou, Qian [1 ]
Wang, Liao-yao [1 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Longhua Hosp, Acupuncture Dept, 725 South Wanping Rd, Shanghai 200032, Peoples R China
[2] Fudan Univ, Huashan Hosp, Dept Geriatr, Shanghai 200040, Peoples R China
[3] Shanghai Jiao Tong Univ, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr, Sch Med, Shanghai 200030, Peoples R China
关键词
Alzheimer's disease; Acupuncture; Syndrome differentiation; Randomized controlled trial; Study protocol; OLDER-ADULTS; ASSESSMENT SCALE; GALANTAMINE; DIAGNOSIS; DEMENTIA; PATTERNS; DEFICITS; CRITERIA; QUALITY; CHINA;
D O I
10.1186/s13063-022-06532-1
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: There has been a rapid increase in the worldwide prevalence of Alzheimer's disease (AD). Previous studies have shown that acupuncture can improve neurological and cognitive function; however, the utility of applying acupuncture in patients with AD remains unclear. This study protocol describes a clinical trial for evaluating the efficacy and safety of acupuncture based on syndrome differentiation with donepezil hydrochloride on cognitive function in patients with AD. Methods/design: This multicenter randomized controlled trial commenced on February 1, 2019, at the Shanghai Longhua Hospital of TCM, Shanghai Huashan Hospital of Fudan University, and Shanghai Mental Health Center, and will conclude on June 30, 2022. The study will recruit 184 patients randomly divided into an acupuncture group or a control group at a 1:1 ratio. All participants will receive donepezil hydrochloride (5 mg/day), and those in the acupuncture group will receive acupuncture based on syndrome differentiation with donepezil for 12 weeks. The primary outcome will be the post-treatment change in the Alzheimer's Disease Assessment Scale-cognition score at 12 weeks. The secondary outcomes will be the efficacy scores of the Minimum Mental State Examination, Alzheimer's Disease Cooperative Research Activity-Daily Life, and Quality of Life-Alzheimer's Disease. All assessments will be performed at baseline, after treatment (week 12), and at follow-up (weeks 24 and 36). Discussion: This trial may provide high-quality evidence for the efficacy of acupuncture in the treatment of AD. The results of this study will be published in peer-reviewed journals.
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页数:11
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