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审核状态: Project audit state: |
通过审核 Successful |
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注册号: Registration number: |
ChiCTR2300068658 |
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最近更新日期: Date of Last Refreshed on: |
2023-05-18 22:24:51 |
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注册时间: Date of Registration: |
2023-02-27 00:00:00 |
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注册号状态: |
预注册 |
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Registration Status: |
Prospective registration |
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注册题目: |
多模态磁共振精准定位下的rTMS对卒中后认知障碍的疗效和机制研究 |
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Public title: |
Study on the effect of rTMS based on precise localization with multimodal magnetic resonance imaging in post-stroke cognitive impairment patients |
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注册题目简写: |
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English Acronym: |
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研究课题的正式科学名称: |
多模态磁共振精准定位下的rTMS对卒中后认知障碍的疗效和机制研究 |
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Scientific title: |
Study on the effect of rTMS based on precise localization with multimodal magnetic resonance imaging in post-stroke cognitive impairment patients |
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研究课题代号(代码): Study subject ID: |
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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: |
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申请注册联系人: |
李亚梅 |
研究负责人: |
李亚梅 |
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Applicant: |
Yamei Li |
Study leader: |
Yamei Li |
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申请注册联系人电话: Applicant telephone: |
18608050988 |
研究负责人电话:
Study leader's |
18608050988 |
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申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
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申请注册联系人电子邮件: Applicant E-mail: |
306592581@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
306592581@qq.com |
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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): |
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申请注册联系人通讯地址: |
四川省成都市青羊区一环路西二段32号 |
研究负责人通讯地址: |
四川省成都市青羊区一环路西二段32号 |
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Applicant address: |
No. 32 West Second Section, First Ring Road, Chengdu 610072, Sichuan, China |
Study leader's address: |
No. 32 West Second Section, First Ring Road, Chengdu 610072, Sichuan, China |
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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: |
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申请人所在单位: |
四川省医学科学院·四川省人民医院 |
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Applicant's institution: |
Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital |
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研究负责人所在单位: |
四川省医学科学院·四川省人民医院 |
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Affiliation of the Leader: |
Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital |
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是否获伦理委员会批准: |
是 |
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Approved by ethic committee: |
Yes |
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伦理委员会批件文号: Approved No. of ethic committee: |
伦审(研)2022年第218-1号 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
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批准本研究的伦理委员会名称: |
四川省医学科学院·四川省人民医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2022-06-16 00:00:00 | ||
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伦理委员会联系人: |
曹柳 |
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Contact Name of the ethic committee: |
Liu Cao |
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伦理委员会联系地址: |
四川省成都市青羊区一环路西二段32号 |
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Contact Address of the ethic committee: |
No. 32 West Second Section, First Ring Road, Chengdu 610072, Sichuan, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 28 87393318 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
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研究实施负责(组长)单位: |
四川省医学科学院·四川省人民医院 |
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Primary sponsor: |
Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital |
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研究实施负责(组长)单位地址: |
四川省成都市青羊区一环路西二段32号 |
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Primary sponsor's address: |
No. 32 West Second Section, First Ring Road, Chengdu 610072, Sichuan, China |
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试验主办单位(项目批准或申办者): Secondary sponsor: |
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经费或物资来源: |
四川省科技计划资助 |
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Source(s) of funding: |
supported by Sichuan Science and Technology Program |
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研究疾病: |
卒中后认知障碍 |
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Target disease: |
post-stroke cognitive impairment (PSCI) |
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研究疾病代码: |
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Target disease code: |
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研究类型: |
干预性研究 |
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Study type: |
Interventional study |
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研究所处阶段: |
治疗新技术临床试验 | ||||||||||||||||||||||
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Study phase: |
New Treatment Measure Clinical Study |
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研究设计: |
横断面 |
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Study design: |
Cross-sectional |
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研究目的: |
1. 建立基于rs-fMRI 和高分辨率T1结构像的rTMS线圈定位方法 2. 观察多模态MRI定位下的rTMS 对PSCI的疗效 3. 基于多模态MRI角度,揭示rTMS改善PSCI认知功能的机制 |
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Objectives of Study: |
1.To Establish a rTMS coil positioning method based on rs-fMRI and high-resolution T1 structural MRI 2. To observe the effect of rTMS on PSCI under multi-modal MRI positioning 3. To uncover the underlying mechanisms of cognitive improvement of PSCI caused by rTMS based on multi-modal MRI |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
①首次卒中,病灶位于左侧,病程≤1 月;②年龄45-75 岁;③右利手;④有认知功能障碍(MMSE、MoCA);⑤入组前未服用影响认知功能的药物;⑥神志清楚,能配合完成治疗及检查者;⑦无其他严重躯体及颅内病变(肿瘤、感染等);⑧患者或其家属签署知情同意书。 |
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Inclusion criteria |
1. First stroke, the lesion was located on the left side, and the duration was less than one month; 2. Aged from 45 to 75years; 3. Right-handed; 4. Cognitive dysfunction (MMSE, MoCA); 5. No drugs affecting cognitive function were taken before enrollment; 6. Being conscious and able to cooperate with the treatment and examination; 7. No other serious physical and intracranial lesions (tumor, infection, etc.); 8. Patients or their family members sign informed consent forms. |
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排除标准: |
①病情不平稳,进展型卒中;②反复发作脑卒中;③多发病灶脑卒中;④既往有癫痫、认知障碍或精神病史;⑤合并严重心、肺、肝、肾功能障碍或其他严重躯体疾病;⑥其他原因所致的认知障碍;⑦体内有金属异物或有其它植入体电子装置或有颅骨缺损;⑧无法合作者。 |
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Exclusion criteria: |
1. The disease is unstable or progressive stroke; 2. Recurrent stroke; 3. Multiple focal stroke; 4. Past history of epilepsy, cognitive impairment or mental illness; 5. Complicated with severe dysfunction of heart, lung, liver, kidney or other serious physical diseases; 6. Cognitive impairment caused by other reasons; 7. Have metal foreign body or other implanted electronic device or skull defect; 8. Patients cannot cooperate. |
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研究实施时间: Study execute time: |
从 From 2022-01-01 00:00:00至 To 2023-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2023-03-01 00:00:00 至 To 2023-08-31 00:00:00 |
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干预措施: Interventions: |
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研究实施地点: Countries of recruitment and research settings: |
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测量指标: Outcomes: |
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采集人体标本:
Collecting sample(s)
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征募研究对象情况: Recruiting status: |
正在进行 Recruiting |
年龄范围: Participant age: |
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性别: |
男女均可 |
Gender: |
Both |
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随机方法(请说明由何人用什么方法产生随机序列): |
按随机数字表进行随机分组:将研究对象按纳入顺序编号,由专人(不参与研究实施)在随机数字表中,任意指定行和列,从左到右依次读取60个两位数,按读取顺序与研究对象编号对应,再按从小到大的顺序将随机数字排序,如果随机数相同,按先后顺序,先出现的为小,排序后序号为1-20对应的对象分为治疗组1,20-40的分为治疗组2,41-60的分为对照组。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Grouping according to random number table: subjects were numbered according to the order of inclusion, A staff (not involved in the implementation) arbitrary specified a row and a column in random number table, from left to right in turn read 60 double digits. Then sort the numbers from smallest to |
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是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
公开/Public |
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盲法: |
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Blinding: |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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是否共享原始数据: IPD sharing |
否No |
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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): |
无,如果所投杂志需要则提供给杂志 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
None, it would be provided to the medical journal if required |
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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: |
1.临床资料和量表由研究人员收集并整理为电子版存档;2.MRI数据由移动硬盘保存,以用作分析 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
1.Clinical data and scales will be collected and archived electronically by researchers; 2.MRI data will be saved by mobile HD for analysis |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |