强化tDCS对抑郁症伴自杀观念的快速起效的研究-双盲随机对照试验

注册号:

Registration number:

ChiCTR2200063271 

最近更新日期:

Date of Last Refreshed on:

2023-04-13 19:09:27 

注册时间:

Date of Registration:

2022-09-02 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

强化tDCS对抑郁症伴自杀观念的快速起效的研究-双盲随机对照试验

Public title:

Adjunctive double-time performed transcranial direct current stimulation (tDCS) for the treatment of depressive patients with suicidal ideation: a double-blind, randomized, sham-controlled trial

注册题目简写:

English Acronym:

研究课题的正式科学名称:

强化tDCS对抑郁症伴自杀观念的快速起效的研究-双盲随机对照试验

Scientific title:

Adjunctive double-time performed transcranial direct current stimulation (tDCS) for the treatment of depressive patients with suicidal ideation: a double-blind, randomized, sham-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:

陈依明 

研究负责人:

陈依明 

Applicant:

Yiming Chen 

Study leader:

Yiming Chen 

申请注册联系人电话:

Applicant telephone:

+86 18818210800

研究负责人电话:

Study leader's
telephone:

+86 18818210800

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:

chenyiming2012@yeah.net

研究负责人电子邮件:

Study leader's E-mail:

chenyiming2012@yeah.net

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:

上海市徐汇区宛平南路600号

研究负责人通讯地址:

上海市徐汇区宛平南路600号

Applicant address:

600 Wanping Road South, Xuhui District, Shanghai

Study leader's address:

600 Wanping Road South, Xuhui District, Shanghai

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:

上海市精神卫生中心

Applicant's institution:

Shanghai Mental Health Center

研究负责人所在单位:

上海市精神卫生中心

Affiliation of the Leader:

Shanghai Mental Health Center

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:

2021-72R

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:

上海市精神卫生中心伦理委员会

Name of the ethic committee:

Ethics Committee of Shanghai Mental Health Center

伦理委员会批准日期:

Date of approved by ethic committee:

2022-08-09 00:00:00

伦理委员会联系人:

黄晶晶

Contact Name of the ethic committee:

Jingjing Huang

伦理委员会联系地址:

上海市徐汇区宛平南路600号

Contact Address of the ethic committee:

600 Wanping Road South, Xuhui District, Shanghai

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:

上海市精神卫生中心

Primary sponsor:

Shanghai Mental Health Center

研究实施负责(组长)单位地址:

上海市徐汇区宛平南路600号

Primary sponsor's address:

600 Wanping Road South, Xuhui District, Shanghai

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

上海市

市(区县):

Country:

China

Province:

Shanghai

City:

单位(医院):

上海市精神卫生中心

具体地址:

上海市徐汇区宛平南路600号

Institution
hospital:

Shanghai Mental Health Center

Address:

600 Wanping Road South, Xuhui District, Shanghai

经费或物资来源:

上海市精神卫生中心“研究型医师培养和能力提升计划”

Source(s) of funding:

Shanghai Mental Health Center "Research Physician Training and Capacity Improvement Program"

研究疾病:

抑郁障碍  

Target disease:

Depressive disorder

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:

探索性研究/预试验 

Study phase:

0

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

1.以抑郁症伴有自杀观念的患者为研究对象,采用随机双盲对照试验,明确强化DLPFC-tDCS快速缓解自杀观念及抑郁症状的疗效及安全性; 2.探究WBC、CRP、NLR、MLR、PLR、NGF、BDNF、GDNF、IL、TNF-a、sTNFr1、sTNFr2在治疗过程中的变化以及与自杀观念、抑郁症状好转之间的关联,从而探究能够预测自杀风险的血清学标志物。  

Objectives of Study:

1. To test the acute improvement on SI and depressive symptoms with the adjunctive daily double-time performed tDCS in MDD patients with antidepressants; 2. To investigate the potential association among variation of WBC, CRP, NLR, MLR, PLR, NGF, BDNF, GDNF, IL, TNF-a, sTNFr1, sTNFr2 and SI in MDD patients treated by adjunctive tDCS.

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.经《简明国际神经精神访谈》访谈(MINI)排除抑郁症以外的其它轴I精神障碍;
2.急、慢性肾功能衰竭者;肝硬化或活动性肝病者;
3.实验室检查异常且判定为有临床意义,研究者认为其影响试验疗效或影响受试者安全的情况;
4.患有严重或不稳定的躯体疾病,包括:神经系统疾病(谵妄、痴呆、中风、癫痫、偏头痛、高颅压、颅脑手术等)、充血性心衰、心绞痛、心肌梗塞、心律失常、高血压(含未经治疗或无法控制的高血压)、呼吸暂停综合征、恶性肿瘤、免疫功能低下受试者及血糖高于12mmol/L受试者;
5.试验开始前30天内酗酒或者试验前6个月内存在酒精或药物依赖者;
6.妊娠期、哺乳期妇女。男、女性受试者未采取有效避孕措施,或计划于开始试验后3月内受(授)孕者;
7.有癫痫家族史(指两系三代以内);
8.皮肤颅骨状况:电极放置部位异常,如有开放伤口等;
9.近期服用苯二氮卓类、抗癫痫类心境稳定剂者(以药物5个半衰期为计算标准);
10.研究者认为存在不适合参加该临床试验的其他情况。

Exclusion criteria:

1. Assessed through applying the Mini-International Neuropsychiatric Interview (MINI) by professional psychiatrists that diagnosed any other current or past psychiatric axis-I disorders (except MDD in the patients);
2. Acute or chronic renal failure, cirrhosis or active hepatopathy;
3. Any clinically significant abnormal laboratory examination that may influence the health of participants;
4. A history of any aignificant medical illness such as neurological disorders (such as cerebral trauma, seizure disorder, etc);
5. Current alcohol and drug abuse;
6. Pregnant women or lactation;
7. Abnormal scalp such as open wounds;
8. Recently taking benzodiazepines and anti-epileptic mood stabilizers (5 half-life of the drug as standard);
9. MDD patients with the treatment in any form prior to the study;
10. There were other conditions that were deemed by the investigator to be inappropriate for participation in the trial.

研究实施时间:

Study execute time:

From 2021-10-01 00:00:00 To 2024-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2022-09-01 00:00:00 To 2024-06-01 00:00:00

干预措施:

Interventions:

组别:

1

样本量:

35

Group:

1

Sample size:

干预措施:

DLPFC经颅直流电刺激

干预措施代码:

Intervention:

active DLPFC tDCS

Intervention code:

组别:

2

样本量:

35

Group:

2

Sample size:

干预措施:

伪DLPFC经颅直流电刺激

干预措施代码:

Intervention:

sham DLPFC tDCS

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

上海市 

市(区县):

 

Country:

China

Province:

Shanghai

City:

单位(医院):

上海市精神卫生中心 

单位级别:

三级甲等 

Institution
hospital:

Shanghai Mental Health Center

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

贝克自杀意念量表

指标类型:

主要指标

Outcome:

Beck Scale for Suicide Ideation

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):

采用计算机随机数生成器。

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

Patients are randomly assigned to either of two groups-the active tDCS group and the sham tDCS group based on a computer-generated randomization scheme stratified by the study staff.

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

否No

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):

使用SPSS录入

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

Recorded by SPSS.

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:

病例记录表

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

Case Record Form

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2022-09-02 23:24:37