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注册号: Registration number: |
ChiCTR2500112337 |
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最近更新日期: Date of Last Refreshed on: |
2025-11-12 16:26:11 |
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注册时间: Date of Registration: |
2025-11-12 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: |
基于融合感知技术与人工智能的左旋多巴负荷试验评测在帕金森综合征诊断应用的前瞻性临床研究 |
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Public title: |
A prospective clinical study on the evaluation of levodopa challenge test based on fusion sensing technology and artificial intelligence for the diagnosis of Parkinson's syndrome. |
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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: |
基于融合感知技术与人工智能的左旋多巴负荷试验评测在帕金森综合征诊断应用的前瞻性临床研究 |
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Scientific title: |
A prospective clinical study on the evaluation of levodopa challenge test based on fusion sensing technology and artificial intelligence for the diagnosis of Parkinson's syndrome. |
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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: |
马凌燕 |
研究负责人: |
冯涛 |
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Applicant: |
Lingyan Ma |
Study leader: |
Tao Feng |
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申请注册联系人电话: Applicant telephone: |
+86 13520873987 |
研究负责人电话:
Study leader's |
+86 13911125339 |
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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: |
Jennifer_MLY@163.com |
研究负责人电子邮件: Study leader's E-mail: |
happyft@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: |
北京市丰台区花乡街道南四环西路119号 |
研究负责人通讯地址: |
北京市丰台区南四环西路119号 |
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Applicant address: |
No. 119, South Fourth Ring West Road, Huaxiang Street, Fengtai District, Beijing |
Study leader's address: |
119 South Fourth Ring West Road, 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: |
首都医科大学附属北京天坛医院 |
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Applicant's institution: |
Beijing Tiantan Hospital affiliated to Capital Medical University |
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研究负责人所在单位: |
首都医科大学附属北京天坛医院 |
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Affiliation of the Leader: |
Beijing Tiantan Hospital, Capital 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: |
KY2024-347-02 |
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: |
首都医科大学附属北京天坛医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Beijing Tiantan Hospital Affiliated to Capital Medical University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-01-07 00:00:00 | ||
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伦理委员会联系人: |
梁晓珊 |
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Contact Name of the ethic committee: |
Liang XiaoShan |
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伦理委员会联系地址: |
北京市丰台区南四环西路119号 |
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Contact Address of the ethic committee: |
119 South Fourth Ring West Road, 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 59975692 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
liangxiaoshan127@126.com |
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研究实施负责(组长)单位: |
首都医科大学附属北京天坛医院 |
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Primary sponsor: |
Beijing Tiantan Hospital, Capital Medical University |
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研究实施负责(组长)单位地址: |
北京市丰台区南四环西路119号 |
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Primary sponsor's address: |
119 South Fourth Ring West Road, 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: |
深圳市臻络科技有限公司 |
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Source(s) of funding: |
GYENNO SCIENCE CO., LTD. |
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研究疾病: |
帕金森病。 |
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Target disease: |
Parkinson's disease. |
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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: |
诊断试验 |
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Study type: |
Diagnostic test |
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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: |
诊断试验诊断准确性 |
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Study design: |
Diagnostic test for accuracy |
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研究目的: |
针对新发、未规范服用左旋多巴制剂、病程小于3年的帕金森综合征患者,采用传统运动范式与新型运动范式相结合,评估受试者进行左旋多巴冲击试验用药前后的运动症状,进行定期随访并修正诊断。整个过程中应用机器视觉、可穿戴等融合感知技术对运动症状进行检测、识别与捕捉,进而利用特定人工智能模型进行诊断,探索其与经典诊断方法的性能差异。 |
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Objectives of Study: |
For patients with newly diagnosed Parkinsonian syndrome who have not undergone standardized levodopa treatment and have a disease duration of less than 3 years, this study combines traditional and novel motor paradigms to assess motor symptoms before and after levodopa challenge tests. Through periodic follow-ups and diagnostic adjustments, the research employs integrated sensing technologies including machine vision and wearable devices to detect, recognize, and capture motor manifestations. Specialized artificial intelligence models are subsequently utilized for diagnostic purposes, aiming to explore performance differences compared to classical diagnostic methods throughout the process. |
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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. 严重认知功能障碍,无法完成评估范式; |
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Exclusion criteria: |
1. Severe cognitive impairment making assessment difficult; |
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研究实施时间: Study execute time: |
从 From 2024-08-01 00:00:00至 To 2029-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-12-31 00:00:00 至 To 2029-12-31 00:00:00 |
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诊断试验: Diagnostic Tests: |
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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): |
无 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
None |
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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: |
无 |
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Blinding: |
None |
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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): |
研究结束后,在公开发表的学术论文中公布,可与Jennifer_MLY@163.com联系获取。 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Upon completion of the study, the findings will be published in peer-reviewed academic journals. For access, please contact Jennifer_MLY@163.com. |
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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: |
数据通过EDC采集和管理数据。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Data will be collected and managed through EDC. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |