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注册号: Registration number: |
ChiCTR2500109631 |
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最近更新日期: Date of Last Refreshed on: |
2025-09-23 11:53:59 |
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注册时间: Date of Registration: |
2025-09-23 00:00:00 |
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注册号状态: |
补注册 |
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Registration Status: |
Retrospective registration |
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注册题目: |
PRO-CTCAE在中国成人型弥漫性胶质瘤患者中 的效度、信度、反应度评估 |
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Public title: |
Validity and Reliability Evaluation of the PRO-CTCAE for Adult-type Diffuse Gliomas Patients in China |
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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: |
基于不良事件通用术语患者自我报告版本 (PRO-CTCAE)在中国成人型弥漫性胶质瘤患者中 的效度、信度、反应度评估 |
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Scientific title: |
Validity and Reliability Evaluation of the Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) for Adult-type Diffuse Gliomas Patients in Chinese Population |
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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: |
吴劲松 |
研究负责人: |
吴劲松 |
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Applicant: |
Jinsong Wu |
Study leader: |
Wu Jinsong |
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申请注册联系人电话: Applicant telephone: |
+86 21 52887200 |
研究负责人电话:
Study leader's |
+86 21 52887200 |
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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: |
wjsongc@126.com |
研究负责人电子邮件: Study leader's E-mail: |
wjsongc@126.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: |
上海市静安区乌鲁木齐中路 12 号 |
研究负责人通讯地址: |
上海市静安区乌鲁木齐中路 12 号 |
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Applicant address: |
No. 12, Middle Road Wu Lu Mu Qi, Jing'an, Shanghai, China |
Study leader's address: |
No. 12, Middle Road Wu Lu Mu Qi, Jing'an, Shanghai, 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: |
复旦大学附属华山医院 |
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Applicant's institution: |
Huashan Hospital, Fudan University |
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研究负责人所在单位: |
复旦大学附属华山医院 |
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Affiliation of the Leader: |
Huashan Hospital, Fudan 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: |
(2022)临审第(681)号 |
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: |
复旦大学附属华山医院伦理审查委员会 |
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Name of the ethic committee: |
Institutional Review Board Huashan Hospital Fudan University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2022-07-12 00:00:00 | ||
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伦理委员会联系人: |
全菁 |
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Contact Name of the ethic committee: |
Quan Jing |
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伦理委员会联系地址: |
上海市静安区乌鲁木齐中路 12 号 |
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Contact Address of the ethic committee: |
No. 12, Middle Road Wu Lu Mu Qi, Jing'an, Shanghai, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 21 52888921 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
quanjing1975@163.com |
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研究实施负责(组长)单位: |
复旦大学附属华山医院 |
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Primary sponsor: |
Huashan Hospital, Fudan University |
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研究实施负责(组长)单位地址: |
上海市静安区乌鲁木齐中路 12 号 |
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Primary sponsor's address: |
No. 12, Middle Road Wu Lu Mu Qi, Jing'an, Shanghai, 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: |
自选课题(自筹) |
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Source(s) of funding: |
self-financing |
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研究疾病: |
成人型弥漫性胶质瘤:包括星形细胞瘤,IDH突变型;少突胶质细胞瘤,IDH突变伴1p/19q联合缺失型;胶质母细胞瘤,IDH野生型;其他成人型弥漫性胶质瘤NEC/NOS |
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Target disease: |
Adult diffuse glioma: including astrocytoma, IDH-mutant; oligodendroglioma, IDH-mutant and1p/19qcodeleted; glioblastoma, IDH-wildtype; other adult diffuse glioma NEC/NOS. |
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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: |
观察性研究 |
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Study type: |
Observational 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: |
连续入组 |
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Study design: |
Sequential |
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研究目的: |
本研究拟针对中国成人型弥漫性胶质瘤患者,首先在资料查阅、胶质瘤专家咨询会调研,专家调查法(Delphi法)、与调查数据分析的基础上,在确定针对成人型弥漫性胶质瘤患者PRO-CTCAE™ 的条目后,开展一项前瞻性、非干预性、多中心的真实世界研究,评估基于不良事件通用术语患者自我报告版本(PRO-CTCAE™ )在中国成人型弥漫性胶质瘤患者结构效度(通过确证性因子分析方法评估观测数据产生的结构与概念性框架的一致性)、重测信度(用于评价量表的可重复性)、反应度(当潜在现象发生变化时,量表显示变化的能力)。 |
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Objectives of Study: |
This study intends to conduct a prospective, non-interventional, multi-center real-world study on China adult diffuse glioma patients, firstly on the basis of data review, glioma expert consultation survey, expert survey method (Delphi method) and survey data analysis, and after determining PRO-CTCAE™ items for adult diffuse glioma patients, To assess construct validity (consistency of the structure generated from observed data with the conceptual framework assessed by confirmatory factor analysis), test-retest reliability (used to evaluate the repeatability of the scale), and responsiveness (ability of the scale to show changes when underlying phenomena change) in China adult diffuse glioma patients based on the patient-reported version of common terms for adverse events (PRO-CTCAE™). |
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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.研究者认为的不适合参加本研究的患者。 |
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Exclusion criteria: |
1.Patients who are not considered suitable for this study. |
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研究实施时间: Study execute time: |
从 From 2022-08-17 00:00:00至 To 2025-01-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2022-09-02 00:00:00 至 To 2024-09-30 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: |
结束 /Completed |
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): |
邮件联系研究者申请数据共享。原始数据EDC项目网址:https://edc.trial.link/project/2027/0/3997/subjects |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Email the investigator to request data sharing. Original Data EDC Project:https://edc.trial.link/project/2027/0/3997/subjects |
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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: |
电子采集和管理系统EDC:https://edc.trial.link/project/2027/0/3997/subjects |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Electronic capture and management system EDC:https://edc.trial.link/project/2027/0/3997/subjects |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |