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注册号: Registration number: |
ChiCTR2600116408 |
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最近更新日期: Date of Last Refreshed on: |
2026-01-09 11:01:04 |
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注册时间: Date of Registration: |
2026-01-09 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: |
脑机接口技术驱动下肢功能性电刺激改善脑卒中患者下肢功能:一项多中心、随机对照试验 |
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Public title: |
Brain-Computer Interface-Driven Functional Electrical Stimulation for Improving Lower Extremities Function in Patients with stroke: A Multicenter, Randomized Controlled Trial |
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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: |
脑机接口技术驱动下肢功能性电刺激改善脑卒中患者下肢功能:一项多中心、随机对照试验 |
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Scientific title: |
Brain-Computer Interface-Driven Functional Electrical Stimulation for Improving Lower Extremities Function in Patients with stroke: A Multicenter, Randomized Controlled Trial |
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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: |
何玮韬 |
研究负责人: |
侯景明 |
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Applicant: |
He Weitao |
Study leader: |
Hou Jingming |
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申请注册联系人电话: Applicant telephone: |
+86 23 68766407 |
研究负责人电话:
Study leader's |
+86 23 68766388 |
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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: |
Hewt1124@outlook.com |
研究负责人电子邮件: Study leader's E-mail: |
jingminghou@hotmail.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: |
中国重庆市沙坪坝区高滩岩正街30号 |
研究负责人通讯地址: |
中国重庆市沙坪坝区高滩岩正街30号 |
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Applicant address: |
No. 30, Gaotanyan Zheng Street, Shapingba District, Chongqing, China |
Study leader's address: |
No. 30, Gaotanyan Zheng Street, Shapingba District, Chongqing, 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: |
中国人民解放军陆军军医大学第一附属医院 |
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Applicant's institution: |
The First Affiliated Hospital of the Army Medical University of PLA |
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研究负责人所在单位: |
中国人民解放军陆军军医大学第一附属医院 |
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Affiliation of the Leader: |
The First Affiliated Hospital of Army Medical University |
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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: |
(A)KY2025174 |
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: |
中国人民解放军陆军军医大学第一附属医院伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of the First Affiliated Hospital of Army Medical University PLA |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-08-19 00:00:00 | ||
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伦理委员会联系人: |
贺莉 |
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Contact Name of the ethic committee: |
He Li |
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伦理委员会联系地址: |
中国重庆市沙坪坝区高滩岩正街30号 |
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Contact Address of the ethic committee: |
No. 30, Gaotanyan Zheng Street, Shapingba District, Chongqing, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 23 68754035 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
cqhl13@qq.com |
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研究实施负责(组长)单位: |
中国人民解放军陆军军医大学第一附属医院 |
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Primary sponsor: |
The First Affiliated Hospital of Army Medical University |
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研究实施负责(组长)单位地址: |
中国重庆市沙坪坝区高滩岩正街30号 |
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Primary sponsor's address: |
No. 30, Gaotanyan Zheng Street, Shapingba District, Chongqing, 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: |
重庆市技术创新重大研发项目 |
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Source(s) of funding: |
Science and Technology Innovation Key R&D Program of Chongqing |
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研究疾病: |
脑梗或脑出血导致的单侧肢体功能障碍 |
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Target disease: |
Unilateral limb dysfunction caused by cerebral infarction or cerebral hemorrhage |
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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: |
其它 | ||||||||||||||||||||||
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Study phase: |
N/A |
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研究设计: |
随机平行对照 |
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Study design: |
Parallel |
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研究目的: |
评估脑机接口技术驱动的下肢功能性电刺激康复治疗,相较于常规康复治疗手段,对脑卒中患者的下肢运动功能、肌肉张力以及日常活动能力的改善情况,并随访观察功能改善的长期效果 |
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Objectives of Study: |
To evaluate the efficacy of brain-computer interface-driven functional electrical stimulation rehabilitation therapy for lower limb function compared to conventional rehabilitation methods in stroke patients, focusing on improvements in lower limb motor function, muscle tone, and activities of daily living. Conduct follow-up observations to assess the long-term effects of functional improvement. |
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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: |
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Inclusion criteria |
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排除标准: |
1.因严重失语症或认知障碍或精神疾病而无法理解或合作; |
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Exclusion criteria: |
1.Inability to comprehend or cooperate due to severe aphasia, cognitive impairment, or psychiatric disorders; |
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研究实施时间: Study execute time: |
从 From 2026-01-12 00:00:00至 To 2027-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2026-01-13 00:00:00 至 To 2027-12-31 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: |
尚未开始 Not yet 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): |
采用基于电子数据采集系统的中心随机化方法进行分配隐藏。由系统内置模块依据预设的区组随机算法生成并维护随机分配序列。符合入选标准的受试者完成基本信息录入后,系统将自动执行随机化分配,并生成一个唯一的随机化编码。该编码与组别信息的对应关系处于盲态,由其监管,仅在试验需要揭盲时方可解锁,以此确保分配过程的公正性与不可预测性。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
The allocation concealment was performed using a centralized randomization method based on an Electronic Data Capture (EDC) system. The built-in system module generated and maintained the randomization sequence according to a pre-established block randomization algorithm. After eligible participants had their baseline information entered, the system automatically executed the randomization assignment and generated a unique randomization code. The correspondence between this code and the actual group assignment remained blinded and under the supervision of Duan Chunyu. It was only to be unlocked at the time of trial unblinding, thereby ensuring the impartiality and unpredictability of the allocation process. |
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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: |
不公开/Private |
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盲法: |
在本研究采用开放标签设计,除患者、BCI 操作人员外,对评估及数据分析人员等所有研究参与人员均设盲。 |
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Blinding: |
This study employed an open-label design, with all other study personnel—including assessors and data analysts—blinded, except for the patients and BCI operators. |
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是否共享原始数据: IPD sharing |
是Yes |
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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): |
在研究主要结果发表1年后,在ResMan公开原始数据 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
One year after the publication of the primary results, the Individual Participant Data will be made publicly available on ResMan. |
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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: |
本研究使用的EDC系统在数据采集、记录、审核、传输等方面都具备严格的要求和流程,以确保临床试验数据的准确性、完整性和安全性。 数据采集:使用电子病例报告表(eCRF),数据管理人员在设计eCRF时对所需采集的数据点进行预先定义,研究人员通过EDC系统直接录入或导入数据。 数据记录:EDC系统支持实时数据录入;EDC系统具有自动记录数据修改痕迹的功能;源数据保存。 数据审核:EDC系统具备自动逻辑核查功能以及人工逻辑核查;配置数据质疑管理模块;源数据核查确认。 数据传输:数据传输过程中应采用加密技术,确保数据在传输过程中的安全性;确保传输的数据完整无损;对于外部数据的传输,应约定明确的传输方法和频率,并规定数据传输失败时的重新传输流程,以确保数据的及时性和完整性。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
The EDC system used in this study adheres to stringent requirements and procedures for data collection, recording, review, and transmission to ensure the accuracy, completeness, and security of clinical trial data.Data Collection: Electronic Case Report Forms (eCRFs) are employed. Data managers predefine required data points during eCRF design, and investigators directly enter or import data through the EDC system.Data Recording: The EDC system supports real-time data entry; it automatically logs data modification traces; source data is preserved.Data Verification: The EDC system incorporates automated and manual logic checks; it includes a data query management module; source data verification and confirmation are performed.Data Transmission: Encryption technology must be employed during data transmission to ensure security; transmitted data integrity must be guaranteed; for external data transfers, explicit transmission methods and frequencies must be agreed upon, along with defined retransmission procedures for failed transfers to ensure timeliness and completeness. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |