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注册号: Registration number: |
ChiCTR2500103622 |
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最近更新日期: Date of Last Refreshed on: |
2025-06-03 10:23:49 |
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注册时间: Date of Registration: |
2025-06-03 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: |
基于人工智能的糖尿病微血管并发症“数字疗法”研发和干预研究 |
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Public title: |
Development and Intervention Study of an AI-Based "Digital Therapeutic" for Diabetic Microvascular Complications |
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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: |
基于人工智能的糖尿病微血管并发症“数字疗法”研发和干预研究 |
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Scientific title: |
Development and Intervention Study of an AI-Based "Digital Therapeutic" for Diabetic Microvascular Complications |
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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: |
林杰滨 |
研究负责人: |
严孙杰 |
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Applicant: |
Jiebin Lin |
Study leader: |
Sunjie Yan |
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申请注册联系人电话: Applicant telephone: |
+86 177 5900 3552 |
研究负责人电话:
Study leader's |
+86 138 0501 5737 |
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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: |
513390939@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
fjyansunjie@163.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: |
福建省福州市茶中路20号 |
研究负责人通讯地址: |
福建省福州市茶中路20号 |
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Applicant address: |
No. 20, Chazhong Road, Fuzhou, Fujian |
Study leader's address: |
No. 20, Chazhong Road, Fuzhou, Fujian |
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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: |
福建医科大学附属第一医院 |
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Applicant's institution: |
The First Affiliated Hospital of Fujian Medical University |
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研究负责人所在单位: |
福建医科大学附属第一医院 |
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Affiliation of the Leader: |
The First Affiliated Hospital of Fujian 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: |
闽医大附一伦理医研[2024]843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: |
福建医科大学附属第一医院医学伦理委员会医学研究与临床技术应用分会 |
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Name of the ethic committee: |
Branch for Medical Research and Clinical Technology Application, Ethics Committee of the First Affiliated Hospital of Fujian Medical University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-10-22 00:00:00 | ||
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伦理委员会联系人: |
张秀秀 |
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Contact Name of the ethic committee: |
Xiuxiu Zhang |
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伦理委员会联系地址: |
福建省台江区茶中路20号福建医科大学附属第一医院 |
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Contact Address of the ethic committee: |
The First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 591 8798 1029 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
fykyk@163.com |
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研究实施负责(组长)单位: |
福建医科大学附属第一医院 |
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Primary sponsor: |
The First Affiliated Hospital of Fujian Medical University |
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研究实施负责(组长)单位地址: |
福建省福州市茶中路20号 |
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Primary sponsor's address: |
No. 20, Chazhong Road, Fuzhou, Fujian |
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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: |
基于人工智能的糖尿病微血管并发症“数字疗法”研发和干预研究(2023ZD0509005),癌症、心脑血管、呼吸和代谢性疾病防治研究国家科技重大专项项目,主持。 |
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Source(s) of funding: |
Principal Investigator, National Key R&D Program Major Project: Development and Intervention of an AI-Based Digital Therapeutic for Diabetic Microvascular Complications (2023ZD0509005), encompassing research on prevention and treatment of cancer, cardiovascular and cerebrovascular, respiratory, and metabolic diseases. |
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研究疾病: |
糖尿病 |
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Target disease: |
Diabetes |
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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: |
探索性研究/预试验 | ||||||||||||||||||||||
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Study phase: |
0 |
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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: |
本项目为临床随机双盲对照试验,旨在通过临床试验分别验证“人工智能技术干预”、“人工教练干预”和“线下常规化糖尿病教育干预”在糖尿病及其并发症防治过程中的有效性。研究将通过比较这三种干预手段在控制血糖水平、减少并发症发生率、改善患者生活质量等方面的效果,以确定相对最优的糖尿病综合管理策略,为糖尿病防治提供科学依据和实践指导。 |
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Objectives of Study: |
This project is a clinical randomized double-blind controlled trial aiming to verify the effectiveness of "Artificial Intelligence Technology Intervention," "Artificial Coach Intervention," and "Offline Conventional Diabetes Education Intervention" in the prevention and treatment of diabetes and its complications through clinical trials. The study will compare the effects of these three interventions in terms of blood sugar control, reduction of complication incidence, and improvement of patient quality of life to determine the relatively optimal comprehensive diabetes management strategy, providing scientific evidence and practical guidance for diabetes prevention and treatment. |
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药物成份或治疗方案详述: |
本项目中所有参与者须通过初步筛选、筛选访视及基线访视三个流程完成研究的筛查及纳入/排除工作,符合筛查及纳入标准的参与者,完成基线访视后通过随机分组分为三个组,即:人工智能技术干预组(下文简称AI 干预)、人工教练干预组及常规化线下糖尿病教育对照组。本项目将对分组至“人工智能技术干预组”、“人工教练干预组”及对照组的参与者分别采取人工智能技术支持或教练线上支持或常规化线下糖尿病教育支持干预的为期12个月的干预,12个月后通过比较两个干预组参与者与对照组参与者的研究结局,包括糖尿病患者代谢指标达标率、糖尿病自我管理能力的变化和糖尿病患者并发症发生及转归。 |
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Description for medicine or protocol of treatment in detail: |
In this project, all participants must go through three processes—initial screening, screening visit, and baseline visit—to complete the screening and inclusion/exclusion work of the study. Participants who meet the screening and inclusion criteria will be randomly divided into three groups after completing the baseline visit: the Artificial Intelligence Intervention Group (hereinafter referred to as AI Intervention), the Human Coach Intervention Group, and the Conventional Offline Diabetes Education Control Group. The project will provide a 12-month intervention for participants in the "Artificial Intelligence Intervention Group," "Human Coach Intervention Group," and control group through AI technology support, online coach support, or conventional offline diabetes education support, respectively. After 12 months, the study outcomes of the participants in the two intervention groups and the control group will be compared, including the rate of achieving metabolic targets in diabetes patients, changes in diabetes self-management abilities, and the occurrence and progression of diabetes complications. |
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纳入标准: |
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Inclusion criteria |
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排除标准: |
1、预期会影响12个月依从和随访的任何状况。 2、智能手机使用障碍,即不能用智能手机发送消息者。 3、已参加其它基于生活方式行为改变的随机对照试验。 4、目前酗酒或滥用非法药物(饮酒过多不是排除标准——这是行为改变的一个潜在目标)。 5、住院或患有其他需要立即住院治疗的急危重症。 6、专科医生或全科医生判断预期生存时间(预期寿命或相关疾病所致)<5年。 7、患有病毒性肝炎、艾滋病或梅毒等性传播疾病,以及处于活动期的结核等传染性疾病。 8、已确诊患有肿瘤。 9、已确诊为下肢动脉的狭窄或闭塞。 |
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Exclusion criteria: |
1, Any condition expected to affect compliance and follow-up for 12 months. 2, Difficulty using a smartphone, specifically the inability to send messages using a smartphone. 3, Participation in other randomized controlled trials based on lifestyle behavior changes. 4, Current alcohol abuse or illegal drug use (excessive alcohol consumption is not an exclusion criterion as it is a potential target for behavior change). 5, Hospitalization or suffering from other acute severe conditions requiring immediate hospitalization. 6, Specialist or general practitioner estimates a life expectancy of less than 5 years due to related diseases. 7, Suffering from sexually transmitted diseases such as viral hepatitis, AIDS, or syphilis, and infectious diseases like active tuberculosis. 8, Diagnosed with cancer. 9, Diagnosed with lower limb arterial stenosis or occlusion. |
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研究实施时间: Study execute time: |
从 From 2024-08-01 00:00:00至 To 2028-07-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-06-15 00:00:00 至 To 2027-06-30 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: |
正在进行 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): |
为了降低选择性偏倚的风险,本研究采用分中心独立随机化方法,将参与者分为三组:AI干预组、人工教练干预组和常规线下糖尿病教育对照组。随机数字序列由一名独立的统计学家使用计算机软件生成,该统计学家不参与参与者的筛选和纳入过程。生成的随机数字序列将按照1:1:1的比例,将参与者均等分配到各组。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
To reduce the risk of selection bias, this study employs a multicenter independent randomization method to divide participants into three groups: the AI intervention group, the human coach intervention group, and the conventional offline diabetes education control group. The random number sequence is generated using computer software by an independent statistician who is not involved in the screening and enrollment of participants. The generated random number sequence will allocate participants equally into the three groups in a 1:1:1 ratio. |
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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: |
双盲,本研究中的施盲对象为:研究对象(患者)与研究人员(医生/评估者)。 |
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Blinding: |
Double-blind, the blinded subjects in this study are: the research subjects (patients) and the researchers (doctors/evaluators). |
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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 |
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): |
公众可以通过团队指定的研究平台或相关网站查询研究计划和进展情况。具体平台为“福建省卫生健康重大科研专项-随机对照试验多中心临床研究平台”,访问链接为:https://swjw.izhangkong.com/#/login?redirect=%2FworkBench%2Findex。 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
The public can check the research plan and progress through the designated research platform or related websites specified by the team. The specific platform is the "Fujian Provincial Health and Wellness Major Scientific Research Project - Randomized Controlled Trial Multicenter Clinical Research Platform," accessible at the following link: https://swjw.izhangkong.com/#/login?redirect=%2FworkBench%2Findex. |
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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: |
利用【AI控糖助手】手机微信小程序,和福建省卫生健康重大科研专项-随机对照试验多中心临床研究平台【链接:https://swjw.izhangkong.com/#/login?redirect=%2FworkBench%2Findex】,建立糖尿病及并发症患者档案,收集防控关键数据。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Utilize the [AI Diabetes Management Assistant] mobile WeChat mini-program and the Fujian Provincial Health and Wellness Major Scientific Research Project - Randomized Controlled Trial Multicenter Clinical Research Platform [link: https://swjw.izhangkong.com/#/login?redirect=%2FworkBench%2Findex] to establish records for patients with diabetes and complications, and to collect key data for prevention and control. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |