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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: |
ChiCTR2600117127 |
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最近更新日期: Date of Last Refreshed on: |
2026-01-20 11:34:51 |
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注册时间: Date of Registration: |
2026-01-20 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: |
基于多模态多任务学习技术的脑卒中首发中西医风险预测模型及健康管理模式的构建 |
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Public title: |
Construction of a Multimodal Multi-Task Learning-Based Integrated Chinese–Western Medicine Model for First-Ever Stroke Risk Prediction and Health Management |
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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: |
基于多模态多任务学习技术的脑卒中首发中西医风险预测模型及健康管理模式的构建 |
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Scientific title: |
Construction of a Multimodal Multi-Task Learning-Based Integrated Chinese–Western Medicine Model for First-Ever Stroke Risk Prediction and Health Management |
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研究课题代号(代码): Study subject ID: |
CXZH2024004 |
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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: |
李彦良 |
研究负责人: |
韩振蕴 |
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Applicant: |
Li Yanliang |
Study leader: |
Han Zhenyun |
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申请注册联系人电话: Applicant telephone: |
+86 131 0450 2052 |
研究负责人电话: Study leader's telephone: |
+86 135 8164 7676 |
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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: |
liyanliang1999@126.com |
研究负责人电子邮件: Study leader's E-mail: |
tohanzhenyun@sina.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: |
北京丰台方庄芳星园一区6号 |
研究负责人通讯地址: |
北京丰台方庄芳星园一区6号 |
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Applicant address: |
No. 6, Area 1, Fangxingyuan, Fangzhuang, Fengtai District, Beijing |
Study leader's address: |
No. 6, Area 1, Fangxingyuan, Fangzhuang, Fengtai District, Beijing |
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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: |
北京中医药大学东方医院 |
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Applicant's institution: |
Dongfang Hospital, Beijing University of Chinese Medicine |
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研究负责人所在单位: |
北京中医药大学东方医院 |
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Affiliation of the Leader: |
Dongfang Hospital, Beijing University of Chinese Medicine |
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是否获伦理委员会批准: |
是/Yes |
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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: |
JDF-IRB-2025035501 |
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: |
北京中医药大学东方医院临床研究伦理委员会 |
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Name of the ethic committee: |
IRB of Dongfang Hospital Beijing University of Chinese Medicine |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-09-14 00:00:00 |
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伦理委员会联系人: |
万洁 |
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Contact Name of the ethic committee: |
Wan Jie |
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伦理委员会联系地址: |
北京丰台方庄芳星园一区6号 |
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Contact Address of the ethic committee: |
No. 6, Area 1, Fangxingyuan, Fangzhuang, Fengtai District, Beijing |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 10 6765 4807 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
dfyyec@126.com |
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研究实施负责(组长)单位: |
北京中医药大学东方医院 |
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Primary sponsor: |
Dongfang Hospital, Beijing University of Chinese Medicine |
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研究实施负责(组长)单位地址: |
北京丰台方庄芳星园一区6号 |
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Primary sponsor's address: |
No. 6, Area 1, Fangxingyuan, Fangzhuang, Fengtai District, Beijing |
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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: |
中国中医药科技发展中心专项经费 30 万元,北京中医药大学东方医院单位匹配经费 30 万元。 |
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Source(s) of funding: |
Specialized funding from China Center for Traditional Chinese Medicine Science and Technology Development (300,000 RMB); Matching funding from Dongfang Hospital, Beijing University of Chinese Medicine (300,000 RMB). |
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Target disease: |
Stroke |
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Target disease code: |
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研究类型: |
观察性研究 |
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Study type: |
Observational study |
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研究所处阶段: |
探索性研究/预试验 | ||||||||||||||||||||||
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Study phase: |
0 |
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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: |
在传统卒中风险因素的基础上广泛采集北京市社区普通老年人群中医症状、证素、证候、体质、中医四诊数据,开展前瞻性横断面研究,分析筛选北京市老年人群卒中西中医风险因素。 |
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Objectives of Study: |
Based on traditional stroke risk factors, TCM-related symptoms, syndrome elements, syndrome types, body constitution, and data from the four diagnostic methods of TCM will be comprehensively collected among community-dwelling older adults in Beijing. A prospective cross-sectional study will be conducted to analyze and identify Western and traditional Chinese medicine risk factors for stroke in this population. |
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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) 65岁及以上的社区常住居民,其中常住居民是指实际经常居住半年以上的人口; (2) 签署知情同意,能配合完成体格检查、实验室检查和中医四诊信息收集。 |
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Inclusion criteria |
(1) Community-dwelling residents aged 65 years or older, where "community-dwelling residents" refers to individuals who have lived in the community for at least six months; (2) Individuals who have provided written informed consent and are able to cooperate with physical examinations, laboratory tests, and the collection of TCM four-diagnostic information. |
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排除标准: |
(1)患有精神疾患、认知或情绪障碍无法理解和(或) 服从研究的程序; (2)有严重原发性疾病,或明显肢体功能障碍,无法配合完成检查者; (3)已具有脑卒中病史。 |
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Exclusion criteria: |
(1) Individuals with psychiatric disorders or cognitive/emotional impairments who are unable to understand and/or comply with study procedures; (2) Individuals with severe primary diseases or significant motor dysfunction that prevents completion of required examinations; (3) Individuals with a documented history of stroke. |
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研究实施时间: Study execute time: |
从 From 2025-04-01 00:00:00至 To 2027-03-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2026-01-21 00:00:00 至 To 2026-12-21 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): |
不适用。本研究为前瞻性观察性研究,不涉及随机分组。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Not applicable. This is a prospective observational study and does not involve random assignment of participants. |
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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 |
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): |
研究完成后6个月内,通过电子邮件向通讯作者申请获取。 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Individual participant data (IPD) will be available upon request via email to the corresponding author within 6 months after the trial completion. |
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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: |
本研究采用电子病例报告表(e-CRF)和电子数据采集系统(EDC)进行数据录入与管理。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Electronic Case Report Form (e-CRF) and Electronic Data Capture (EDC) system are used for data management. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |