Community-based health management in Shanghai
Shanghai Pudong Natural Population-based Cohort Establishment and Follow-up
This study is trying to gather health information from people in Shanghai, from birth to old age, to help improve public health and prevent chronic diseases.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 80000 (estimated) |
| Ages | 0 Years to 120 Years |
| Sex | All |
| Sponsor | RenJi Hospital Academic / other |
| Locations | 1 site (Shanghai) |
| Trial ID | NCT05206643 on ClinicalTrials.gov |
What this trial studies
This observational cohort study aims to establish a natural population-based cohort in Shanghai, China, focusing on the health status of individuals from birth to older age. It integrates questionnaire data and sample databases into a public health information platform to create a comprehensive health management system. The study builds on previous research by collecting extensive health-related data, including chronic disease history and various health parameters, to promote evidence-based public health practices for chronic disease prevention.
Who should consider this trial
Good fit: Ideal candidates include urban and rural residents aged 0 to 120 years in Pudong District, Shanghai, who can provide informed consent.
Not a fit: Patients who are severely ill, frail, or have cognitive, hearing, or speaking problems may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance public health strategies and improve chronic disease prevention across diverse age groups in Shanghai.
How similar studies have performed: Other studies have shown success in using cohort approaches for public health management, indicating that this methodology is both tested and promising.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 0\~120-year-old verified urban and rural residents in Pudong District, Shanghai * Able to give informed consent (or has a legal designee) All the selected samples were to be interviewed. Exclusion Criteria: severely ill or too frail to answer; or having cognitive problems; having hearing or speaking problems; or dementia.
Where this trial is running
Shanghai
- Cardiology, Ren Ji Hospital — Shanghai, China (Recruiting)
Study contacts
- Principal investigator: Jun Pu, MD,PhD — Cardiology, Ren Ji Hospital, Shanghai, China
- Study coordinator: Jun Pu, MD,PhD
- Email: pujun310@hotmail.com
- Phone: 86-21-68383477
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.