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注册号: Registration number: |
ChiCTR2400083558 |
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最近更新日期: Date of Last Refreshed on: |
2024-04-28 14:38:25 |
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注册时间: Date of Registration: |
2024-04-28 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: |
数字疗法改善糖尿病及其并发症管理的有效性和安全性的整群随机、对照、多中心、开放标签临床试验 |
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Public title: |
Effectiveness and safety of the digital therapy to improve the management of diabetes and its complication: A cluster of randomized, controlled, multicenter, open-label clinical trial |
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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: |
数字疗法改善糖尿病及其并发症管理的有效性和安全性的整群随机、对照、多中心、开放标签临床试验 |
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Scientific title: |
Effectiveness and safety of the digital therapy to improve the management of diabetes and its complication: A cluster of randomized, controlled, multicenter, open-label clinical trial |
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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: |
阳晴 |
研究负责人: |
刘芳 |
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Applicant: |
Yang Qing |
Study leader: |
Liu Fang |
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申请注册联系人电话: Applicant telephone: |
+86 183 7333 2106 |
研究负责人电话:
Study leader's |
+86 189 8060 1214 |
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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: |
yangqing2106@163.com |
研究负责人电子邮件: Study leader's E-mail: |
liufangfh@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: |
四川省武侯区四川大学华西临床医学院 |
研究负责人通讯地址: |
四川省武侯区四川大学华西医院 |
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Applicant address: |
West China Clinical Medical College of Sichuan University, Wuhou District, Sichuan Province |
Study leader's address: |
West China hospital of Sichuan University, Wuhou District, Sichuan Province |
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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: |
四川大学华西临床医学院 |
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Applicant's institution: |
West China Clinical Medical College of Sichuan University |
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研究负责人所在单位: |
四川大学华西医院 |
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Affiliation of the Leader: |
West China hospital of Sichuan 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: |
2024年审(536)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: |
四川大学华西医院医学伦理审查委员会 |
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Name of the ethic committee: |
Clinical Trial Ethics Committee of West China Hospital, Sichuan University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-03-28 00:00:00 | ||
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伦理委员会联系人: |
邓邵林 |
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Contact Name of the ethic committee: |
Shaolin Deng |
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伦理委员会联系地址: |
中国四川省成都市武侯区国学巷37号 |
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Contact Address of the ethic committee: |
37 Guoxue Lane, Wuhou District, Chengdu, Sichuan, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 28 8542 3237 |
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: |
四川大学华西医院 |
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Primary sponsor: |
West China Hospital, Sichuan University |
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研究实施负责(组长)单位地址: |
中国四川省成都市武侯区国学巷37号 |
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Primary sponsor's address: |
37 Guoxue Lane, Wuhou District, Chengdu, Sichuan, 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: |
四川省卫生健康委员会 |
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Source(s) of funding: |
Health Commission of Sichuan |
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研究疾病: |
糖尿病及其并发症 |
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Target disease: |
Diabetes and its complication |
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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: |
预后研究 |
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Study type: |
Prognosis 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: |
整群随机分组 |
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Study design: |
Cluster randomization |
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研究目的: |
1. 主要目的: 第一阶段:验证与单纯常规医疗护理相比,在此基础上加上数字疗法是否会进一步降低血糖、血压、血脂水平,改善糖尿病并发症危险因素的控制。(随访1年) 第二阶段:验证与单纯常规医疗护理相比,在此基础上加上数字疗法是否会降低糖尿病并发症的发病率、延缓糖尿病并发症的疾病进展。(随访3年) 2. 次要目的:验证与单纯常规医疗护理相比,在此基础上加上数字疗法是否提高药物治疗、饮食生活习惯改善、运动增加等的依从性。 |
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Objectives of Study: |
1. Primary Objectives: Phase 1: To verify whether digital therapy added to conventional medical care can further reduce blood glucose, blood pressure, and blood lipid levels and improve the control of risk factors for diabetic complications compared with conventional medical care alone. (Follow-up: 1 year) Phase 2: To verify whether digital therapy added to conventional medical care can reduce the incidence of diabetic complications and delay the progression of diabetic complications compared with conventional medical care alone. (Follow-up: 3 years) 2. Secondary Objectives: To verify whether digital therapy added to conventional medical care can improve adherence to medication, diet and lifestyle improvement, and exercise increase compared with conventional medical care alone. |
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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) 哺乳期或孕期女性,或近期有生育计划的女性或男性 2) 预期寿命<3 年 3) 纽约心脏协会 (NYHA) Ⅲ级至 IV 级心力衰竭病史 4) 进入终末期肾脏病的患者:eGFR<15ml或需要持续性透析治疗 5) 侵袭性的细菌、真菌、病毒感染,感染不受控制的患者 6) 活跃的严重慢性肺病或肝病,2年内未缓解的活动性恶性肿瘤性疾病(成功治疗的皮肤鳞状细胞癌和/或基底细胞癌和/或乳腺癌或结肠癌,经手术切除且不需要辅助化疗或放射治疗者除外);血白细胞计数<3.0×10^9/L、血红蛋白<90g/L、血小板计数<100×10^9/L、PT或PTT升高>1.5倍、ANC <1.0×10^9/L、ALT和/或AST>正常的3倍,或有其他血液系统疾病(严重贫血、特发性血小板减少性紫癜、脾肿大、凝血功能障碍等)的患者 7) 研究者认为可能增加参与者的研究风险的任何医疗状况、检查异常、或疾病 8) 无法理解研究的潜在风险和益处、无法律行为能力 |
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Exclusion criteria: |
1) Breastfeeding or pregnant women, or women or men with recent reproductive plans 2) Life expectancy <3 years 3) New York Heart Association (NYHA) grade III to IV heart failure history 4) Entering the end-stage renal disease patients: eGFR <15ml or need continuous dialysis treatment 5) Invasive bacterial, fungal, viral infections, uncontrolled infections 6) Active severe chronic lung or liver disease, 2 years of remission of active malignant tumor disease (successfully treated cutaneous squamous cell carcinoma and/or basal cell carcinoma and/or breast cancer or colon cancer, except for surgical resection and without adjuvant chemotherapy or radiation therapy);blood white blood cell count <3.0×10^9/L, hemoglobin <90g/L, platelet count <100×10^9/L, PT or PTT increased >1.5 times, ANC <1.0×10^9/L, ALT and/or AST >3 times normal, or other blood system diseases (severe anemia, idiopathic thrombocytopenic purpura, splenomegaly, coagulation dysfunction, etc.) 7) Any medical conditions, abnormal examinations, or diseases that the researchers believe may increase the risk of the study participants 8) Unable to understand the potential risks and benefits of the study, incompetent for legal conduct |
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研究实施时间: Study execute time: |
从 From 2025-03-01 00:00:00至 To 2030-03-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-03-01 00:00:00 至 To 2026-03-01 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): |
随机化将根据中心所处地区的社会经济水平进行匹配,将在四川大学华西医院临床设计和统计办公室独立进行。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
The randomization will be matched according to the socioeconomic level of the region in which the centers are located and will be conducted independently in the Clinical Design and Statistics Office of West China Hospital of Sichuan University. |
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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: |
由于设计和干预的性质,收集临床结果数据的研究参与者、初级保健医生、研究护士都是不设盲的。然而,测量 HbA1c、LDL-c 和其他实验室结果的实验室技术人员以及终点裁决委员会成员却隐瞒了分配情况。 |
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Blinding: |
Due to the design and nature of the intervention, study participants, primary care physicians, and study nurses collecting clinical outcome data were not blind. However, laboratory technicians who measured HbA1c, LDL-c and other laboratory results, as well as members of the endpoint adjudication committee, concealed the allocation. |
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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): |
否 |
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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: |
使用CRF表进行数据收集,使用电子采集和管理系统进行数据管理 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
CRF tables are used for data collection and electronic acquisition and management systems are used for data 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 |