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注册号: Registration number: |
ChiCTR2300072017 |
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最近更新日期: Date of Last Refreshed on: |
2023-07-27 16:22:11 |
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注册时间: Date of Registration: |
2023-05-31 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: |
基于人工智能标准化病人的CBL教学模式构建与效果研究——以针对临床专科医师的大肠癌教学为例 |
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Public title: |
Construction and effect research of Artificial Intelligence-based Standardized patient CBL teaching model -- A case study of colorectal cancer teaching for clinical specialists |
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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: |
基于人工智能标准化病人的CBL教学模式构建与效果研究——以针对临床专科医师的大肠癌教学为例 |
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Scientific title: |
Construction and effect research of Artificial Intelligence-based Standardized patient CBL teaching model -- A case study of colorectal cancer teaching for clinical specialists |
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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: |
吴一波 |
研究负责人: |
史江漂 |
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Applicant: |
Yibo Wu |
Study leader: |
Jiangpiao Shi |
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申请注册联系人电话: Applicant telephone: |
+86 188 1016 9630 |
研究负责人电话:
Study leader's |
+86 151 7575 7296 |
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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: |
bjmuwuyibo@outlook.com |
研究负责人电子邮件: Study leader's E-mail: |
1051114056@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: |
中华人民共和国北京市海淀区学院路38号 |
研究负责人通讯地址: |
中华人民共和国河北省保定市唐县向阳北街28号 |
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Applicant address: |
38 Xueyuan Road, Haidian District, Beijing, China |
Study leader's address: |
28 Xiangyang Street North, Tangxian County, Baoding, Hebei, 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: |
北京大学公共卫生学院 |
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Applicant's institution: |
School of Public Health, Peking University, Beijing 100191, China |
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研究负责人所在单位: |
保定市第四中心医院 |
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Affiliation of the Leader: |
The Fourth Central Hospital of Baoding |
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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: |
2023032 |
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: |
保定市第四中心医院伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of the Fourth Central Hospital of Baoding |
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伦理委员会批准日期: Date of approved by ethic committee: |
2023-05-08 00:00:00 | ||
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伦理委员会联系人: |
赵文娟 |
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Contact Name of the ethic committee: |
Wenjuan Zhao |
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伦理委员会联系地址: |
中华人民共和国河北省保定市唐县向阳北街28号 |
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Contact Address of the ethic committee: |
28 Xiangyang Street North, Tangxian County, Baoding, Hebei, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 159 3075 8855 |
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: |
保定市第四中心医院 |
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Primary sponsor: |
The Fourth Central Hospital of Baoding |
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研究实施负责(组长)单位地址: |
中华人民共和国河北省保定市唐县向阳北街28号 |
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Primary sponsor's address: |
28 Xiangyang Street North, Tangxian County, Baoding, Hebei, 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: |
自筹 |
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Source(s) of funding: |
Self-funded |
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研究疾病: |
无 |
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Target disease: |
N/A |
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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: |
探究基于人工智能标准化病人的CBL教学模式的应用效果 |
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Objectives of Study: |
Explore the application effect of artificial intelligence-standardized patient CBL teaching mode |
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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.项目开始前理论考试不合格者 2.正在参加其他课题者 3.参加过标准化病人的CBL教学的结直肠癌培训者 |
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Exclusion criteria: |
1. Failed to pass the theory test before the project began 2. Those who are taking part in other projects 3. Colorectal cancer trainers who have participated in standardized patient CBL teaching |
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研究实施时间: Study execute time: |
从 From 2023-03-01 00:00:00至 To 2023-11-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2023-06-01 00:00:00 至 To 2023-08-01 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): |
随机化分组由史江漂利用Excel随机数(Rand)实施 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Random grouping was implemented by Shi Jiang using Excel random number (Rand) |
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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: |
研究采用单盲原则,为避免资料收集员在收集资料时出现主观偏倚,本研究对资料收集员实施单盲,不告知资料收集员研究对象的分组情况和具体干预内容。 |
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Blinding: |
The study was single-blinded, and to avoid subjective bias in data collection by the data collectors, the study was single-blinded to the data collectors, who were not informed of the grouping of the study subjects or the specific interventions. |
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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 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
none |
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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: |
数据收集:所有的研究结果,包括临床和试验室数据,都将记录在受试者的医疗记录和病例报告表(CRF)中。研究者负责确保CRF的所有部分都正确完成,并可以根据源数据进行验证。每个完成的CRF必须注明日期并签字。一份原始CRF的副本将被转移给试验首席研究员。最初的CRF将留给调查人员。 数据的存储和归档:研究者将将所有试验数据(受试者识别代码列表、源数据和研究者文件)和相关通信存档在研究数据库文件中。数据库所有来源数据和该研究的所有相关文件将在试验定稿后根据法律法规存档。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Data collection: All study results, including clinical and laboratory data, will be recorded in the subject's medical record and case report Form (CRF). The investigator is responsible for ensuring that all parts of the CRF are completed correctly and can be verified against source data. Each completed CRF must be dated and signed. A copy of the original CRF will be transferred to the lead investigator of the trial. The initial CRF will be left to investigators. Storage and archiving of data: The investigator will archive all trial data (subject identification code lists, source data, and investigator files) and related communications in a study database file. All source data of the database and all relevant documents of the study will be archived in accordance with laws and regulations after the trial is finalized. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |