tDCS促进脑卒中患者偏瘫上肢功能恢复的多中心临床随机对照研究

注册号:

Registration number:

ChiCTR1800015881 

最近更新日期:

Date of Last Refreshed on:

2018-04-26 15:22:11 

注册时间:

Date of Registration:

2018-04-26 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

tDCS促进脑卒中患者偏瘫上肢功能恢复的多中心临床随机对照研究

Public title:

Transcranial direct current stimulation for motor recovery of upper limb function after stroke: a multicenter randomized controlled trial

注册题目简写:

English Acronym:

研究课题的正式科学名称:

tDCS促进脑卒中患者偏瘫上肢功能恢复的多中心临床随机对照研究

Scientific title:

Transcranial direct current stimulation for motor recovery of upper limb function after stroke: a multicenter randomized controlled trial

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:

申请注册联系人:

刘慧华 

研究负责人:

刘慧华 

Applicant:

Liu Huihua 

Study leader:

Liu Huihua 

申请注册联系人电话:

Applicant telephone:

+86 15989193467

研究负责人电话:

Study leader's
telephone:

+86 15989193467

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:

872251681@qq.com

研究负责人电子邮件:

Study leader's E-mail:

872251681@qq.com

申请单位网址(自愿提供):

Applicant 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:

广州市沿江西路107号

研究负责人通讯地址:

广州市沿江西路107号

Applicant address:

107 Yanjiang Road West, Guangzhou, Guangdong, China

Study leader's address:

107 Yanjiang Road West, Guangzhou, Guangdong, 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:

中山大学孙逸仙纪念医院

Applicant's institution:

Sun Yat-sen Memorial Hospital, Sun Yat-sen University

研究负责人所在单位:

中山大学孙逸仙纪念医院

Affiliation of the Leader:

Sun Yat-sen Memorial Hospital, Sun Yat-sen University

是否获伦理委员会批准:

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

2018-21

伦理委员会批件附件:

Approved file of Ethical Committee:

查看附件View

批准本研究的伦理委员会名称:

中山大学孙逸仙纪念医院临床研究伦理委员会

Name of the ethic committee:

Research Ethics Committee of Sun Yat-sen Memorial Hospital, Sun Yat-sen University

伦理委员会批准日期:

Date of approved by ethic committee:

2018-02-08 00:00:00

伦理委员会联系人:

林双秀

Contact Name of the ethic committee:

Lin Shuangxiu

伦理委员会联系地址:

广州市沿江西路107号

Contact Address of the ethic committee:

107 Yanjiang Road West, Guangzhou, Guangdong, China

伦理委员会联系人电话:

Contact phone of the ethic committee:

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:

中山大学孙逸仙纪念医院

Primary sponsor:

Sun Yat-sen Memorial Hospital, Sun Yat-sen University

研究实施负责(组长)单位地址:

广州市沿江西路107号

Primary sponsor's address:

107 Yanjiang Road West, Guangzhou, Guangdong, 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):

广东省

市(区县):

广州市

Country:

China

Province:

Guangdong

City:

Guangzhou

单位(医院):

中山大学孙逸仙纪念医院

具体地址:

广州市沿江西路107号

Institution
hospital:

Sun Yat-sen Memorial Hospital, Sun Yat-sen University

Address:

107 Yanjiang Road West, Guangzhou, Guangdong, China

经费或物资来源:

孙逸仙纪念医院逸仙临床研究培育项目

Source(s) of funding:

YiXian Clinical research project of Sun Yat-sen Memorial Hospital

研究疾病:

脑卒中  

Target disease:

stroke

研究疾病代码:

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

治疗新技术临床试验 

Study phase:

New Treatment Measure Clinical Study

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

1 通过临床随机对照研究,明确tDCS作为一种预干预方式,联合传统康复治疗技术,能否增强脑卒中后偏瘫上肢运动功能的康复疗效; 2 利用电生理及影像学检查,探讨其对皮层兴奋性的影响。  

Objectives of Study:

1. To investigate whether tDCS, as a pre-intervention method, combines traditional rehabilitation therapy technology, can enhance the the upper limb recovery after stroke; 2. To investigate the effects of tDCS on cortical excitability by electrophysiological and imaging techniques.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

Inclusion criteria

排除标准:

(1)脑出血后有去骨瓣减压、颅骨修补等手术操作的患者
(2)意识不清,MMSE量表评价提示痴呆,合并感觉性失语或精神障碍等疾患,不能配合检查及治疗的住院患者
(3)合并心、肝、肾和造血系统等严重原发性疾病的患者
(4)既往有认知障碍、神经精神病史、药物滥用及酗酒史
(5)有心脏起搏器,脑刺激装置植入及颅内金属植入装置(动脉夹、颅骨修补)的患者
(6)脑室-腹腔分流术后患者
(7)癫痫经药物治疗未得到良好控制的患者
(8)不能完成基本疗程,依从性可能不好者(即不能坚持治疗)及难以随访者
(9)患侧上肢有金属植入物者

Exclusion criteria:

(1) patients with decompression of bone flap and skull repair after intracerebral hemorrhage;
(2) the MMSE evaluation indicated dementia, or combined with sensory aphasia or mental disorder, and was not able to compliance to examination and treatment;
(3) patients with severe diseases of heart, liver, kidney and hematopoietic system;
(4) previous history of cognitive impairment, neuropsychiatric history, drug abuse and alcoholism;
(5) patients with cardiac pacemakers, brain stimulation devices and intracranial metal implantation devices (artery clamps, skull repair);
(6) patients with ventriculo-peritoneal shunt;
(7) patients with epilepsy who have not been well controlled by drug;
(8) unable to compliance to treatment, and difficult to follow up;
(9) patients with metal implants on the side upper limbs.

研究实施时间:

Study execute time:

From 2018-01-01 00:00:00 To 2021-01-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2018-06-01 00:00:00 To 2020-10-31 00:00:00

干预措施:

Interventions:

组别:

tDCS+基础康复训练组

样本量:

153

Group:

tDCS +routine rehabilitation group

Sample size:

干预措施:

经颅直流电刺激

干预措施代码:

Intervention:

tDCS

Intervention code:

组别:

tDCS安慰刺激+基础康复训练组

样本量:

153

Group:

sham tDCS+routine rehabilitation group

Sample size:

干预措施:

tDCS安慰刺激

干预措施代码:

Intervention:

sham tDCS

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

广东 

市(区县):

广州 

Country:

China

Province:

Guangdong

City:

guangzhou

单位(医院):

中山大学孙逸仙纪念医院 

单位级别:

三级甲等 

Institution
hospital:

Sun Yat-sen Memorial Hospital, Sun Yat-sen University

Level of the institution:

Tertiary A Hospital

国家:

中国

省(直辖市):

广东 

市(区县):

广州 

Country:

China

Province:

Guangdong

City:

guangzhou

单位(医院):

广东三九脑科医院 

单位级别:

三级甲等 

Institution
hospital:

Guangdong sanjiu brain hospital.

Level of the institution:

Tertiary A Hospital

国家:

中国

省(直辖市):

湖北 

市(区县):

十堰 

Country:

China

Province:

Hubei

City:

shiyan

单位(医院):

十堰市太和医院 

单位级别:

三级甲等 

Institution
hospital:

Shiyan Taihe Hospital

Level of the institution:

Tertiary A Hospital

测量指标:

Outcomes:

指标中文名:

改良Ashworth评分

指标类型:

主要指标

Outcome:

MAS

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

Fugl-Meyer上肢运动功能评分

指标类型:

主要指标

Outcome:

FMA

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

功能性磁共振成像

指标类型:

次要指标

Outcome:

fMRI

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

运动诱发电位

指标类型:

次要指标

Outcome:

MEP

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

肌力

指标类型:

主要指标

Outcome:

muscle strength

Type:

Primary 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:

血液

组织:

Sample Name:

blood

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

Note:

征募研究对象情况:

Recruiting status:

尚未开始

Not yet recruiting

年龄范围:

Participant age:

最小 Min age years
最大 Max age years

性别:

男女均可

Gender:

Both

随机方法(请说明由何人用什么方法产生随机序列):

由课题组专业统计学人士采用SAS9.4统计软件产生随机编码,采用中心分层随机的方法,将受试者按照1:1比例随机分配到tDCS+基础康复训练组153例,tDCS安慰刺激+基础康复训练组153例。

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

Statisticians use SAS9.4 generate random code, subjects were randomly assigned to tDCS+routine rehabilitation treatment group(153 cases), sham tDCS+routine rehabilitation treatment group(153 cases), according to the proportion of 1:1, using the method of center stratified random.

是否公开试验完成后的统计结果:

Calculated Results after the Study Completed public access:

不公开/Private

盲法:

Blinding:

是否共享原始数据:

IPD sharing

是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个月内公开上报到临床研究注册网站ClinicalTrials.gov上

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

within six months after the trial complete on ClinicalTrials.gov

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:

数据采集:病例报告表(Case Record Form, CRF) 数据管理:采用Epidata 3.1 进行电子采集及保存

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

Data collection:Case Record Form Management:Epidata 3.1

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2018-04-26 15:22:11