- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06387875
Cohort in Qianwan New District, Ningbo
Prevention and Control of Chronic Noncommunicable Diseases in Natural Population in Qianwan New District, Ningbo
Study Overview
Status
Detailed Description
- Through baseline survey (cross-sectional survey) and prospective cohort design, the health status information and biological samples of residents in Hangzhou Bay Hospital were collected, and the physical, psychological and social adaptability information was collected through questionnaires and other forms, basic tests and omics measurements were carried out based on the collected samples to build a multi-dimensional data platform.
Develop a disease risk prediction model based on big data platform, conduct high-risk population screening and establish risk assessment files; In view of the common health problems in the study population, the key factors and effects of health status were analyzed comprehensively, and the corresponding mathematical model was established to form the prediction of health status. Finally to establish the stratified standard of population health status and provide effective health guidance.
Questionnaire survey on epidemiology: The Hangzhou Bay Natural Population Cohort Questionnaire was designed according to the principles and requirements of cohort study. All respondents who entered the cohort will sign informed consent, receive face-to-face interview with uniformly trained investigators, and the questionnaire will be reviewed by quality control personnel for quality control.
Physical examination: The examination contents include height, weight, blood pressure, waist circumference, hip circumference, hearing, vision, medical history and surgery, inbody composition, chest film, electrocardiogram, B-ultrasound, non-invasive arteriosclerosis examination, vascular endothelial ultrasound and other imaging examinations.
Clinical biochemical test: 5-10 ml of blood, 20 ml of urine and 5 g of feces were collected (if necessary) according to the chronic non-communicable disease spectrum and clinical test requirements in Qianwan New District of Ningbo; The blood samples and urine were tested for biochemistry, liver and kidney function, blood lipids and electrolytes according to clinical testing requirements, as well as multi-omics indicators as needed.
- Prospective study data: Follow-up of the cohort population (disease occurrence, death, migration, etc.) was conducted through annual active follow-up (telephone, interview, etc.) and passive follow-up, including data of all-cause death, incidence of any kind of diseases.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Jun Pu, MD, PhD
- Phone Number: 86-21-68383477
- Email: pujun310@hotmail.com
Study Contact Backup
- Name: Wei Zhang, PhD
- Phone Number: 86-13761780922
- Email: zhangwei050080@renji.com
Study Locations
-
-
-
Shanghai, China
- Recruiting
- Ren Ji Hospital Afflited to School of Medicine, Shanghai Jiao Tong University
-
Contact:
- Jun Pu, MD,PHD
- Phone Number: 86-21-68383477
- Email: pujun310@hotmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- 1) Local permanent residents aged 18 and above (including residents with household registration, or residents without household registration but with a permanent job);
- 2) No serious physical disability, can communicate normally;
- 3) Participate voluntarily and sign informed consent.
Exclusion Criteria:
- 1) Temporary resident and floating population;
- 2) There are serious health conditions unable to participate in the survey;
- 3) Those who are unwilling to accept the follow-up inspection of the project.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
death
Time Frame: 4 years
|
Mortality of all-cause disease were calculated by age, gender and area compared by different health management mode.
|
4 years
|
incidence of cardio-cerebrovascular diseases
Time Frame: 4 years
|
Incidence of Cardiovascular and Cerebrovascular diseases were calculated by age, gender and area compared by different health management mode.
|
4 years
|
incidence of other non-communicable chronic diseases
Time Frame: 4 years
|
Incidence of other non-communicable chronic diseases were calculated by age, gender and area compared by different health management mode.
|
4 years
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Jun Pu, MD, PhD, Ningbo Hangzhou Bay Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Hangzhou Bay Cohort
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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