The efficacy of electro-acupuncture on patients with mild cognitive impairment: a randomized controlled trial

注册号:

Registration number:

ITMCTR1900002571

最近更新日期:

Date of Last Refreshed on:

2019-09-04

注册时间:

Date of Registration:

2019-09-04

注册号状态:

Registration Status:

预注册

Prospective registration

注册题目:

电针治疗遗忘型轻度认知障碍的临床疗效评价

Public title:

The efficacy of electro-acupuncture on patients with mild cognitive impairment: a randomized controlled trial

注册题目简写:

English Acronym:

研究课题的正式科学名称:

电针治疗遗忘型轻度认知障碍的临床疗效评价

Scientific title:

The efficacy of electro-acupuncture on patients with mild cognitive impairment: a randomized controlled trial

研究课题的正式科学名称简写:

Scientific title acronym:

研究课题代号(代码):

Study subject ID:

在二级注册机构或其它机构的注册号:

The registration number of the Partner Registry or other register:

ChiCTR1900025671 ; ChiMCTR1900002571

申请注册联系人:

翟炎冰

研究负责人:

翟炎冰

Applicant:

Zhai Yanbing

Study leader:

Zhai Yanbing

申请注册联系人电话:

Applicant telephone:

+86 15901136071

研究负责人电话:

Study leader's telephone:

+86 15901136071

申请注册联系人传真 :

Applicant Fax:

研究负责人传真:

Study leader's fax:

申请注册联系人电子邮件:

Applicant E-mail:

zhaiyanbing0617@163.com

研究负责人电子邮件:

Study leader's E-mail:

zhaiyanbing0617@163.com

申请单位网址(自愿提供):

Study leader's website(voluntary supply):

研究负责人网址(自愿提供):

Study leader's website
(voluntary supply):

申请注册联系人通讯地址:

北京市丰台区芳星园1区6号

研究负责人通讯地址:

北京市丰台区芳星园1区6号

Applicant address:

6 Fangxingyuan, Block 1, Fengtai District, Beijing, China

Study leader's address:

6 Fangxingyuan, Block 1, Fengtai District, Beijing, China

申请注册联系人邮政编码:

Applicant postcode:

研究负责人邮政编码:

Study leader's postcode:

申请人所在单位:

北京中医药大学东方医院康复科

Applicant's institution:

Department of Rehabilitation, Dongfang Hospital, Beijing University of Chinese Medicine

是否获伦理委员会批准:

Approved by ethic committee:

伦理委员会批件文号:

Approved No. of ethic committee:

JDF-IRB-2019031902

伦理委员会批件附件:

Approved file of Ethical Committee:

View

批准本研究的伦理委员会名称:

北京中医药大学东方医院临床研究伦理委员会

Name of the ethic committee:

IRB of Dongfang Hospital, Beijing University of Chinese Medicine

伦理委员会批准日期:

Date of approved by ethic committee:

2019/6/10 0:00:00

伦理委员会联系人:

夏芸

Contact Name of the ethic committee:

Xia Yun

伦理委员会联系地址:

北京市丰台区芳星园1区6号北京中医药大学东方医院

Contact Address of the ethic committee:

6 Fangxingyuan, Block 1, Fengtai District, Beijing, China

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 010-67654807

伦理委员会联系人邮箱:

Contact email of the ethic committee:

研究实施负责(组长)单位:

北京中医药大学东方医院

Primary sponsor:

Dongfang Hospital Beijing University of Chinese Medicine

研究实施负责(组长)单位地址:

北京市丰台区芳星园1区6号北京中医药大学东方医院

Primary sponsor's address:

6 Fangxingyuan, Block 1, Fengtai District, Beijing, China

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

北京市

市(区县):

Country:

China

Province:

Beijing

City:

单位(医院):

北京中医药大学东方医院

具体地址:

丰台区芳星园1区6号

Institution
hospital:

Dongfang Hospital Beijing University of Chinese Medicine

Address:

6 Fangxingyuan, Block 1, Fengtai District

经费或物资来源:

北京中医药大学东方医院

Source(s) of funding:

Dongfang Hospital Beijing University of Chinese Medicine

研究疾病:

轻度认知障碍

研究疾病代码:

Target disease:

Mild Cognitive Impairment

Target disease code:

研究类型:

Study type:

干预性研究

Interventional study

研究设计:

Study design:

随机平行对照

randomized controlled trial(parallel group design)

研究所处阶段:

Study phase:

探索性研究/预试验

Pilot clinical trial

研究目的:

主要目的:验证电针治疗MCI的有效性和安全性,并比较不同频次电针改善MCI的疗效。 次要目的:通过12周的随访,观察不同频次电针改善MCI患者认知障碍的后治疗效应,疗效持续时间,以及对延缓病程进展的影响。

Objectives of Study:

Primary purpose: to verify the efficacy and safety of EA in the treatment of MCI and to compare the different frequency efficacy of EA in improving MCI. Secondary purpose: 1.through 12 weeks follow-up, observe the duration of curative effects of different frequency of EA on patients with MCI. 2.through 12 weeks follow-up, observe the effect on delaying the progress of the disease.

药物成份或治疗方案详述:

Description for medicine or protocol of treatment in detail:

纳入标准:

① 符合Petersen等提出的MCI诊断标准; ② 年龄符合50~85岁; ③ 中文版简易精神状态检查(MMSE)为24-30分、中文版蒙特利尔认知评估量表(MOCA)小于26分; ④ 客观记忆测查分值低于年龄文化匹配1.5SD; ⑤ 临床痴呆评定量表(CRD)评分为0.5分,其中记忆领域分数≥0.5分;总体衰退量表(GDS)评级为2-3级; ⑥ 签署知情同意书; ⑦ 有相对固定的住址或联系电话,可进行随访者。

Inclusion criteria

1. Complying with the diagnostic criteria of MCI proposed by Petersen; 2. Aged 50-85 years; 3. MMSE 24-30, MOCA < 26; 4. The score of objective memory test was lower than 1.5SD of age-culture matching; 5. CDR 0.5,Memory box score >= 0.5, GDS rated level 2-3. 6. Willing to signed the informed consent form; 7. With permanent address or phone number for follow up.

排除标准:

① Hachinski缺血之数量表(HIS)得分>4分者; ② 汉密尔顿抑郁量表得分>8分者; ③ 近6个月内甲状腺功能检查可诊断为甲状腺功能减低者; ④ 患有严重的心、肝、肾、造血系统、内分泌系统疾病、全身营养状况不良的患者; ⑤ 诊断有其他影响认知功能的疾病,如阿尔兹海默症、路易体病、正常颅压脑积水等; ⑥ 文化程度为文盲者,或严重失语(理解困难、表达困难者),或视力严重下降者、失明者,或有意识障碍,或因肢体障碍不能配合相关测查者; ⑦ 有酗酒或精神类药物滥用史者。

Exclusion criteria:

1. Significant cerebral vascular disease Modified Hachinski > 4; 2. Hamilton Depression Rating Scale > 8; 3. In recent 6 months,thyroid function examination can be diagnosed as hypothyroidism; 4. With severe heart, liver, kidney, hematopoietic system, endocrine system diseases, or systemic malnutrition; 5. Presenting other disease-associated cognitive dysfunction,such us Alzheimer's disease,Lewy body disease,NPH etc.; 6. Illiteracy,or severe aphasia,or severe vision dysfunction,or disturbance of consciousness,or suffered from physical impairment that can not be tested with the relevant examines; 7. With a history of alcohol or psychotropic substance abuse.

研究实施时间:

Study execute time:

From 2019-01-01

To      2020-12-31

征募观察对象时间:

Recruiting time:

From 2019-09-09

To      2020-06-30

干预措施:

Interventions:

组别:

电针A组

样本量:

20

Group:

Group A

Sample size:

干预措施:

电针/一周三次

干预措施代码:

Intervention:

Electro-acupuncture/3 times per week

Intervention code:

组别:

电针B组

样本量:

20

Group:

Group B

Sample size:

干预措施:

电针/一周一次

干预措施代码:

Intervention:

Electro-acupuncture/1 time per week

Intervention code:

样本总量 Total sample size : 40

研究实施地点:

Countries of recruitment
and research settings:

国家:

中国

省(直辖市):

北京市

市(区县):

Country:

China

Province:

Beijing

City:

单位(医院):

北京中医药大学东方医院

单位级别:

三级甲等

Institution/hospital:

Dongfang Hospital Beijing University of Chinese Medicine

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

工具性日常生活活动能力量表

指标类型:

次要指标

Outcome:

Instrumental Activities of Daily Living

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

蒙特利尔认知评估

指标类型:

次要指标

Outcome:

Montreal Cognitive Assessment

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

简易智能精神状态检查量表

指标类型:

主要指标

Outcome:

Mini-mental State Examination

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

阿尔茨海默病评定量表-认知部分

指标类型:

次要指标

Outcome:

Alzheimer’s Disease Assessment Scale-Cognitive section

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

组织:

Sample Name:

N/A

Tissue:

人体标本去向

其它

说明

Fate of sample 

Others

Note:

征募研究对象情况:

正在进行

Recruiting

年龄范围:

最小
Min age years
最大
Max age years

Recruiting status:

Participant age:

性别:

Gender:

男女均可

Both

随机方法(请说明由何人用什么方法产生随机序列):

采用密闭信封法,进行区组随机。借助SAS软件PROC PLAN过程语句进行区组随机分组,Block设计为4,设定A为治疗组,B为对照组,按照纳入顺序将研究对象编号为1-40号,得出与纳入顺序号相对应的随机分配组别,即两组各20例。

Randomization Procedure (please state who generates the random number sequence and by what method):

Use SAS software PROC PLAN procedure to generate the randomintion list.Eligible participants were randomly allocated to either group A(treatment group) or group B(control group) in a ratio of 1:1 by this randomintion list.

盲法:

因治疗组与对照组采用电针治疗频次不一致,故无法完成盲法设计。为了使研究中已知的偏倚来源达到最小,采用疗效评价者盲法,即观察过程中,量表评测均由不知分组情况的专职评价者负责。达到观察指标评价、记录、数据录入者和针刺操作者及统计人员三分离。

Blinding:

Blind method for evaluators.

是否共享原始数据:

IPD sharing:

Yes

共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址):

试验完成后6个月内公开于百度网盘:https://pan.baidu.com/。

The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url):

Within six months after trial complete.Website:https://pan.baidu.com/.

数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC:

数据均记录在纸质版病例记录表中(CRF),并由专人收集与管理。

Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture:

All the date will be collected in the Case Record Form(CRF) by specially-assigned person.

数据管理委员会:

Data Managemen Committee:

暂未确定

Not yet

研究计划书或研究结果报告发表信息
(杂志名称、期、卷、页,时间;或网址):

Publication information of the protocol/research results report
(name of the journal, volume, issue, pages, time; or website):

ITMCTR BJ-ICP:07032215-5 Tip: IE8 is recommended Use the system with widescreen display resolution above