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注册号: Registration number: |
ChiCTR2400091324 |
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最近更新日期: Date of Last Refreshed on: |
2024-10-25 16:25:40 |
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注册时间: Date of Registration: |
2024-10-25 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: |
简短言语干预促进流感疫苗接种的机制、开发与验证研究 |
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Public title: |
Mechanisms, Development, and Validation of Rapid Verbal Persuasion in Promoting Influenza Vaccination UpTake |
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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: |
简短言语干预促进流感疫苗接种的机制、开发与验证研究 |
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Scientific title: |
Mechanisms, Development, and Validation of Rapid Verbal Persuasion in Promoting Influenza Vaccination UpTake |
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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: |
朱俊林 |
研究负责人: |
徐东;刘思源 |
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Applicant: |
Junlin Zhu |
Study leader: |
Dong Xu;Siyuan Liu |
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申请注册联系人电话: Applicant telephone: |
+86 157 7572 7746 |
研究负责人电话:
Study leader's |
+86 139 1098 8979 |
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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: |
junlin7746@gmail.com |
研究负责人电子邮件: Study leader's E-mail: |
roman.xu@gmail.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: |
广东省广州市白云区沙太南路1023号 |
研究负责人通讯地址: |
广东省广州市白云区沙太南路1023号 |
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Applicant address: |
1023 Shatai Road South, Baiyun District, Guangzhou, Guangdong, China |
Study leader's address: |
1023 Shatai Road South, Baiyun District, Guangzhou, Guangdong, China |
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申请注册联系人邮政编码: Applicant postcode: |
510515 |
研究负责人邮政编码: Study leader's postcode: |
510515 |
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申请人所在单位: |
南方医科大学卫生管理学院 |
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Applicant's institution: |
School of Health Management, Southern Medical University |
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研究负责人所在单位: |
南方医科大学卫生管理学院 |
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Affiliation of the Leader: |
School of Health Management, Southern 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: |
南医伦审[2024]第52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: |
南方医科大学生物医学伦理委员会 |
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Name of the ethic committee: |
Biomedical Ethics Committee of Southern Medical University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-09-10 00:00:00 | ||
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伦理委员会联系人: |
马俊 |
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Contact Name of the ethic committee: |
Jun Ma |
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伦理委员会联系地址: |
南方医科大学行政楼215 |
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Contact Address of the ethic committee: |
Room 215, Administration Building, Southern Medical University |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 20 6164 7452 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
majun11@smu.edu.cn |
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研究实施负责(组长)单位: |
南方医科大学 |
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Primary sponsor: |
Southern Medical University |
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研究实施负责(组长)单位地址: |
广东省广州市白云区沙太南路1023号 |
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Primary sponsor's address: |
1023 Shatai Road South, Baiyun District, Guangzhou, Guangdong, 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: |
瑞士发展与合作署 |
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Source(s) of funding: |
Swiss Agency for Development and Cooperation |
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研究疾病: |
流行性感冒 |
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Target disease: |
influenza |
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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: |
验证针对流感疫苗的简短言语干预是否能够提高流感疫苗的接种率。 |
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Objectives of Study: |
To validate whether a rapid verbal persuasion for the flu vaccine can increase vaccination rates for the flu vaccine. |
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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.对于医疗机构,排除标准为: 曾参与其他流感疫苗接种率提升相关研究的医疗机构。 2.对于研究对象,排除标准为: (1)主动前往医疗机构接种流感疫苗的群众; (2)在当前流感流行季节已经接种过流感疫苗的群众。 |
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Exclusion criteria: |
1. For medical institutions, the exclusion criteria are: medical institutions that have previously participated in other studies related to improving flu vaccination rates. 2. For research subjects, the exclusion criteria are: (1) individuals who actively visit medical institutions to receive the flu vaccine; (2) individuals who have already received the flu vaccine during the current flu season. |
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研究实施时间: Study execute time: |
从 From 2024-10-28 00:00:00至 To 2025-03-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2024-10-28 00:00:00 至 To 2025-03-01 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): |
执行干预的医务人员会按照事先生成的随机数字序列,将入组的群众分配到干预组和对照组中的一个。具体步骤如下: 1.生成随机数字:一位独立于研究团队之外的统计学家使用统计软件R生成一组随机数字,确保这些数字是均匀分布的,以达到公平分配的目的; 2.设定分组规则:决定每个组的比例(1:1),确保每两名参与者中有一名被分配到干预组,另一名进入对照组; 3.分配过程:在入组时,医务人员根据参与者的顺序,依次查阅随机数字列表。根据事先设定的规则(偶数数字分配到干预组,奇数数字分配到对照组),将参与者随机分配到相应的组。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
The healthcare personnel responsible for implementing the intervention will assign the enrolled participants to either the intervention group or the control group based on a pre-generated random number sequence. The specific steps are as follows: 1. Generation of Random Numbers: A statistician, independent of the research team, will use statistical software R to generate a set of random numbers, ensuring that the numbers are uniformly distributed to achieve a fair allocation. 2. Setting the Grouping Rules: A 1:1 ratio will be established, ensuring that for every two participants, one is assigned to the intervention group and the other to the control group. 3. Allocation Process: Upon enrollment, the healthcare personnel will consult the random number list in the order of participant recruitment. According to the pre-set rule (even numbers assigned to the intervention group, odd numbers to the control group), participants will be randomly allocated to the corresponding group. |
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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: |
由于干预措施的性质,受试者、医务人员知晓受试者被分配到的研究组,而研究负责人员、数据收集者、数据分析人员不知晓受试者被分配到的研究组。 |
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Blinding: |
Due to the nature of the intervention, both the subjects and healthcare personnel are aware of the group assignment, while the research staff, data collectors, and data analysts remain unaware of the participants' group assignments. |
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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 |
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): |
研究数据采集结束后,经过一年的数据保护期,相关研究人员可根据合理需求向通讯作者索取原始数据。 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
After the completion of data collection, and following a one-year data protection period, relevant researchers may request the original data from the corresponding author based on reasonable needs. |
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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: |
本试验采用电子病例报告表(CRF),所有数据通过红帽系统(REDCap)采集和管理。REDCap是免费且功能强大的数据采集、储存和管理的云工具。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
This trial uses electronic case report forms (CRF), with all data collected and managed through the REDCap system. REDCap is a free and powerful cloud-based tool for data collection, storage, and management. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |