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Clinical Trials in China / NCT07207863
Recruiting Observational

Tianshan Community Cohort Establishment and Follow-up

NCT07207863 · tracked via the Priya Life Science China tracker
Sponsor
People's Hospital of Xinjiang Uygur Autonomous Region
Phase
Observational
Started
2016-01-01
Last updated
2025-10-06

Condition(s) studied

Cohort StudyNatural PopulationNorthwest Region of China

Study summary

This population-based cohort study on disease prevention and health promotion was established in northwest China, leveraging data from routine annual health examinations. Initiated in January 2016, the cohort enrolled nearly all residents aged 18 years and older who were registered at community healthcare centers. The program was developed to provide a comprehensive framework for disease prevention and community health promotion, with the aim of producing population-based evidence across a broad spectrum of diseases in the general population. At baseline, data were collected on participant demographics, medical and family histories, disability status, living environment, and blood biochemical parameters. Follow-up information is primarily obtained through chronic disease management programs, annual health examinations, and electrical health records. Cause-specific mortality is ascertained from local death registration systems. Biological specimens, questionnaire data, and electrical health records are systematically archived in the Biobank and Big Data Center of the People's Hospital of Xinjiang Uygur Autonomous Region.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
Accepted
Inclusion Criteria: 1. Residents \>=18y 2. Permanent residents or individuals who have lived in the region for more than 5 years and are enrolled in local social security medical insurance 3. Residents without severe physical disability and capable of normal communication 4. Residents whose diseases and deaths are monitored and managed by the local health authorities 5. Residents who voluntarily participate and provide written informed consent Exclusion Criteria: 1. Temporary residents or floating population 2. Residents with severe health conditions that prevent participation in the study 3. Residents who are unwilling to undergo follow-up assessments for the study

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
People's Hospital of Xinjiang Uygur Autonomous Region Ürümqi Xinjiang Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07207863 on ClinicalTrials.gov ↗ ← All trials in China