|
审核状态: Project audit state: |
通过审核 Successful |
|
注册号: Registration number: |
ChiCTR2600123368 |
|
最近更新日期: Date of Last Refreshed on: |
2026-04-26 14:48:22 |
|
注册时间: Date of Registration: |
2026-04-26 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
基于太极拳动作优化的上肢康复机器人改善脑卒中患者运动功能障碍的多中心临床研究 |
|
Public title: |
A multicenter clinical study on the improvement of motor dysfunction in stroke patients with upper limb rehabilitation robot based on Tai Chi movement optimization |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
基于太极动作优化的上肢康复机器人改善脑卒中患者运动功能障碍的多中心临床研究 |
|
Scientific title: |
A multicenter clinical study on the improvement of motor dysfunction in stroke patients with upper limb rehabilitation robot based on Tai Chi movement optimization |
|
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: |
万芮含 |
研究负责人: |
万芮含 |
|
Applicant: |
Wan Ruihan |
Study leader: |
Wan Ruihan |
|
申请注册联系人电话: Applicant telephone: |
+86 187 5124 2707 |
研究负责人电话:
Study leader's |
+86 187 5124 2707 |
|
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: |
wanruih@163.com |
研究负责人电子邮件: Study leader's E-mail: |
wanruih@163.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: |
中国江苏省南京市鼓楼区丁家桥87号 |
研究负责人通讯地址: |
中国江苏省南京市鼓楼区丁家桥87号 |
|
Applicant address: |
87 Dingjiaqiao, Gulou District, Nanjing, Jiangsu, China |
Study leader's address: |
87 Dingjiaqiao, Gulou District, Nanjing, Jiangsu, 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: |
东南大学附属中大医院 |
||
|
Applicant's institution: |
Zhongda Hospital Affiliated to Southeast University |
||
|
研究负责人所在单位: |
东南大学附属中大医院 |
||
|
Affiliation of the Leader: |
Zhongda Hospital Affiliated to Southeast University |
||
|
是否获伦理委员会批准: |
是 |
||
|
Approved by ethic committee: |
Yes |
||
|
伦理委员会批件文号: Approved No. of ethic committee: |
2026ZDSYLL086-P01 |
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: |
东南大学附属中大医院临床研究伦理委员会 |
||
|
Name of the ethic committee: |
IEC for clinical Research of Zhangda Hospital Southeast University |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2026-04-07 00:00:00 | ||
|
伦理委员会联系人: |
李拥军 |
||
|
Contact Name of the ethic committee: |
Li Yongjun |
||
|
伦理委员会联系地址: |
中国江苏省南京市鼓楼区丁家桥87号 |
||
|
Contact Address of the ethic committee: |
87 Dingjiaqiao, Gulou District, Nanjing, Jiangsu, China |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 155 5083 5629 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
ZDLL2015@163.com |
|
研究实施负责(组长)单位: |
东南大学附属中大医院 |
||||||||||||||||||||||
|
Primary sponsor: |
Zhongda Hospital Affiliated to Southeast University |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
中国江苏省南京市鼓楼区丁家桥87号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
87 Dingjiaqiao, Gulou District, Nanjing, Jiangsu, China |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
自筹 |
||||||||||||||||||||||
|
Source(s) of funding: |
Self-funded |
||||||||||||||||||||||
|
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: |
其它 | ||||||||||||||||||||||
|
Study phase: |
N/A |
||||||||||||||||||||||
|
研究设计: |
随机平行对照 |
||||||||||||||||||||||
|
Study design: |
Parallel |
||||||||||||||||||||||
|
研究目的: |
探究基于太极拳训练的上肢机器人辅助训练对脑卒中患者上肢治疗恢复的影响,并基于脑肌耦合(fNIRS-sEMG)探讨可能的效应机制。以期为脑卒中上肢功能康复方案提供参考。 |
||||||||||||||||||||||
|
Objectives of Study: |
To investigate the effect of upper limb robot-assisted training based on Tai Chi training on upper limb treatment recovery in stroke patients, and to explore the possible mechanism of effect based on brain-muscle coupling (fNIRS-sEMG). In order to provide a reference for the functional rehabilitation plan of the upper limb of stroke. |
||||||||||||||||||||||
|
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. 符合脑卒中的诊断标准,并经头颅CT或MRI检查证实; 2. 年龄18~80岁,性别不限; 3. 首次脑卒中,2周≤病程≤6个月; 4. 存在中重度上肢运动障碍,即Fugl-Meyer上肢功能评分为8~38分; 5. 可以理解并配合完成本研究使用的上肢康复机器人训练,且能独立坐位维持时间不少于45min; 6. 自愿参加并签署知情同意书。 |
||||||||||||||||||||||
|
Inclusion criteria |
1. Meets the diagnostic criteria for stroke and is confirmed by cranial CT or MRI 2. aged 18-80 years, regardless of gender 3. first-ever stroke, with a disease duration of 2 weeks to 6 months 4. presence of moderate to severe upper limb motor impairment, defined as a Fugl-Meyer Upper Extremity Assessment score of 8-38 5. able to understand and cooperate with the upper limb rehabilitation robot training used in this study, and able to maintain independent sitting for at least 45 minutes 6. willing to participate and sign the informed consent form. |
||||||||||||||||||||||
|
排除标准: |
1. 神经科医生根据世界卫生组织《国际疾病分类》第 10 版(ICD-10)和《精神疾病诊断与统计手册》第五版(DSM-V)诊断标准排除痴呆、精神疾病患者; 2. 合并严重的内科疾病、生命体征不稳定,不能完成该研究中任务活动的患者; 3. 合并偏瘫侧肢体骨折、严重感染及严重肝肾功能损伤的患者等; 4. 因创伤、骨折、关节痉挛等造成的肩、肘、腕关节挛缩; 5. 正在参与其他临床研究影响本研究结果者。 |
||||||||||||||||||||||
|
Exclusion criteria: |
1. Patients with dementia or psychiatric disorders, as excluded by a neurologist according to the diagnostic criteria of the International Classification of Diseases, 10th Revision (ICD-10) issued by the World Health Organization and the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5); 2. Patients with severe internal medical diseases, unstable vital signs, or inability to complete the task activities required in this study; 3. Patients with fractures of the hemiplegic limb, severe infection, severe hepatic or renal dysfunction, or other serious comorbid conditions; 4. Patients with contractures of the shoulder, elbow, or wrist joints caused by trauma, fracture, or joint spasticity; 5. Patients currently participating in other clinical studies that may affect the results of this study. |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2026-05-01 00:00:00至 To 2028-12-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2026-05-01 00:00:00 至 To 2028-12-01 00:00:00 |
|
干预措施: Interventions: |
|
|
研究实施地点: Countries of recruitment and research settings: |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
测量指标: Outcomes: |
|
|
采集人体标本:
Collecting sample(s)
|
|
|
征募研究对象情况: Recruiting status: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
|
||||||
|
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): |
区组随机,一个与试验不相关的统计专家在一个不透光的信封内保存随机分组方案 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
A statistician, uninvolved in the trial, held the random assignment scheme in an opaque sealed envelope. |
||||||||
|
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: |
单盲(对受试者隐藏分组),对评估者隐藏分组 |
|
Blinding: |
A single-blind design was adopted, in which group allocation was concealed from the participants and the outcome assessors. |
|
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): |
无 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
not have |
|
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: |
病历记录表 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
CRF |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |