ChiCTR2400092553 版本V1.0 版本创建时间2024/11/19 10:50:41 中国临床试验注册中心

审核状态:

Project audit state:

通过审核

Successful

注册号:

Registration number:

ChiCTR2400092553 

最近更新日期:

Date of Last Refreshed on:

2024-11-19 10:50:14 

注册时间:

Date of Registration:

2024-11-19 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

基于AI与穿戴技术的老年肌少症风险识别与个性化预防策略研究

Public title:

Risk identification and personalized prevention strategy for elderly sarcopenia based on AI and wearable technology

注册题目简写:

English Acronym:

研究课题的正式科学名称:

基于AI与穿戴技术的老年肌少症风险识别与个性化预防策略研究

Scientific title:

Risk identification and personalized prevention strategy for elderly sarcopenia based on AI and wearable technology

研究课题代号(代码):

Study subject ID:

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:

申请注册联系人:

邓一平 

研究负责人:

岳冀蓉 

Applicant:

Yiping Deng 

Study leader:

Jirong Yue 

申请注册联系人电话:

Applicant telephone:

+86 28 85421550

研究负责人电话:

Study leader's
telephone:

+86 28 85421550

申请注册联系人传真 :

Applicant Fax:

研究负责人传真:

Study leader's fax:

申请注册联系人电子邮件:

Applicant E-mail:

dengyiping@wchscu.cn

研究负责人电子邮件:

Study leader's E-mail:

yuejirong11@hotmail.com

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):

申请注册联系人通讯地址:

四川省成都市武侯区国学巷37号

研究负责人通讯地址:

四川省成都市武侯区国学巷37号

Applicant address:

37 Guoxue Lane, Wuhou District, Chengdu, Sichuan

Study leader's address:

37 Guoxue Lane, Wuhou District, Chengdu, Sichuan

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:

申请人所在单位:

四川大学华西医院

Applicant's institution:

West China Hospital, Sichuan University

研究负责人所在单位:

四川大学华西医院

Affiliation of the Leader:

West China Hospital of Sichuan University

是否获伦理委员会批准:

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

2024年审(1925)号

伦理委员会批件附件:

Approved file of Ethical Committee:

查看附件View

批准本研究的伦理委员会名称:

四川大学华西医院伦理委员会

Name of the ethic committee:

Ethics Committee of West China Hospital of Sichuan University

伦理委员会批准日期:

Date of approved by ethic committee:

2024-10-11 00:00:00

伦理委员会联系人:

李娜

Contact Name of the ethic committee:

Li Na

伦理委员会联系地址:

四川省成都市武侯区国学巷37号

Contact Address of the ethic committee:

37 Guoxue Lane, Wuhou District, Chengdu, Sichuan

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 28 85422654

伦理委员会联系人邮箱:

Contact email of the ethic committee:

188974152@qq.com

研究实施负责(组长)单位:

四川大学华西医院

Primary sponsor:

West China Hospital of Sichuan University

研究实施负责(组长)单位地址:

四川省成都市武侯区国学巷37号

Primary sponsor's address:

37 Guoxue Lane, Wuhou District, Chengdu, Sichuan

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

四川

市(区县):

Country:

China

Province:

Sichuan

City:

单位(医院):

四川大学华西医院

具体地址:

四川省成都市武侯区国学巷37号

Institution
hospital:

West China Hospital of Sichuan University

Address:

37 Guoxue Lane, Wuhou District, Chengdu, Sichuan

经费或物资来源:

四川省科技计划项目

Source(s) of funding:

Sichuan Province science and technology plan project

研究疾病:

肌少症  

Target disease:

sarcopenia

研究疾病代码:

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

探索性研究/预试验 

Study phase:

0

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

探索基于肌少症 AI 辅助决策支持系统和移动健康技术的社区老年肌少症管理模式  

Objectives of Study:

To explore a community management model of sarcopenia for elderly people based on AI-assisted decision support system and mobile health technology

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

1.在当地居住时间不少于 36 个月,未来 3 年不会离开;
2.年龄在 60 周岁或以上;
3.小学及以上学历;
4.已与所在社区卫生服务中心签订家庭医生团队服务合约;
5.拥有并能够使用智能手机;
6.自愿参加本研究并签署知情同意书;
7.经 PRE-SARC 评估确定为老年肌少症高风险;

Inclusion criteria

1.Live there for at least 36 months and will not leave for the next 3 years;
2.Age 60 or above;
3.Primary school or above;
4.A family doctor team service contract has been signed with the local community health service center;
5.Own and be able to use a smartphone;
6.Volunteer to participate in the study and sign the informed consent;
7.The PRE-SARC assessment identified a high risk of sarcopenia;

排除标准:

1.诊断为脑卒中、冠心病或心肌梗死及严重心功能不全(NYHA III 或 IV 级);
2.需要紧急处理的疾病,如急性感染、高血压危象、糖尿病酮症酸中毒等;
3.肝肾功能严重异常,存在自身免疫病或其他严重致命疾病;
4.已诊断患有各种恶性肿瘤;
5.存在精神系统疾患或酗酒问题,无法自我控制或表达意愿;
6.严重体力活动受限,卧床不能站立;
7.无法配合或明确拒绝参加本研究;

Exclusion criteria:

1.Diagnosis of stroke coronary heart disease or myocardial infarction and severe cardiac insufficiency (NYHA III or IV); 2.Diseases requiring urgent treatment, such as acute infection, hypertensive crisis, diabetic ketoacidosis, etc; 3.Severe abnormal liver and kidney function, the presence of autoimmune disease or other serious fatal diseases; 4.Has been diagnosed with various malignancies; 5.Have a psychiatric disorder or alcohol problem and are unable to exercise self-control or express their will; 6.Severely limited physical activity, bedridden and unable to stand; 7.Unable to cooperate with or explicitly refused to participate in the study;

研究实施时间:

Study execute time:

From 2024-10-01 00:00:00 To 2025-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2024-12-01 00:00:00 To 2025-12-31 00:00:00

干预措施:

Interventions:

组别:

个体化干预组

样本量:

399

Group:

Individualized intervention group

Sample size:

干预措施:

AI 辅助决策干预

干预措施代码:

Intervention:

AI assisted decision intervention

Intervention code:

组别:

常规干预组

样本量:

399

Group:

Routine intervention group

Sample size:

干预措施:

传统健康教育

干预措施代码:

Intervention:

Traditional health education

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

四川 

市(区县):

 

Country:

China

Province:

Sichuan

City:

单位(医院):

四川大学华西医院 

单位级别:

三级甲等 

Institution
hospital:

West China Hospital of Sichuan University

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

重庆 

市(区县):

 

Country:

China

Province:

Chongqing

City:

单位(医院):

重庆医科大学附属第一医院 

单位级别:

三级甲等 

Institution
hospital:

The First Affiliated Hospital of Chongqing Medical University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

PRE-SARC 的风险值改变、肌少症的发生率、肌肉质量、肌肉力量和躯体功能等肌少症相关指标的改善情况,以及肌少症相关不良结局(跌倒、骨折、再入院、失能、死亡)的发生率

指标类型:

主要指标

Outcome:

The improvement of sarcopenia-related indicators such as changes in risk value of PRE-SARC, incidence of sarcopenia, muscle mass, muscle strength and physical function, as well as the incidence of sarcopenia-related adverse outcomes (falls, fractures, readmission, disability, and death)

Type:

Primary indicator

测量时间点:

干预实施后的第 6 个月和第 12个月

测量方法:

Measure time point of outcome:

6 and 12 months after the intervention

Measure method:

指标中文名:

肌少症危险因素的改变情况(如吸(戒)烟率、体力活动情况、饮酒率、膳食习惯)

指标类型:

次要指标

Outcome:

Changes in risk factors for sarcopenia (such as smoking cessation rate, physical activity, alcohol consumption rate, dietary habits)

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

健康相关指标(如心率、血压、血氧、小腿围、上臂中围、腰围、臀围、体重指数(BMI)、体脂分布)的改变情况

指标类型:

次要指标

Outcome:

Changes in health-related indicators such as heart rate, blood pressure, blood oxygen, calf circumference, upper arm circumference, waist circumference, hip circumference, body mass index (BMI), and body fat distribution

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

营养状况(营养不良评分、血肌酐、eGFR、血糖、白蛋白、糖化血红蛋白等)的改变情况

指标类型:

次要指标

Outcome:

Changes in nutritional status (malnutrition score, creatinine, eGFR, blood glucose, albumin, glycated hemoglobin, etc.)

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

生活质量的改变

指标类型:

次要指标

Outcome:

Changes in quality of life

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

组织:

Sample Name:

NA

Tissue:

人体标本去向

其它  

说明

Fate of sample:

0thers  

Note:

征募研究对象情况:

Recruiting status:

尚未开始

Not yet recruiting

年龄范围:

Participant age:

最小 Min age 60 years
最大 Max age 99 years

性别:

男女均可

Gender:

Both

随机方法(请说明由何人用什么方法产生随机序列):

随机数字表

Randomization Procedure (please state who generates the random number sequence and by what method):

Random number table

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

盲法:

对评估者设盲

Blinding:

Blinding evaluators

是否共享原始数据:

IPD sharing

是Yes

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):

发表文章后;邮件联系

The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url):

After publishing the paper; Contact by email

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:

CRF

Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture:

CRF

数据与安全监察委员会:

Data and Safety Monitoring Committee:

无/No

注册人:

Name of Registration:

 2024-11-19 10:50:14