Tianshan Community Cohort Establishment and Follow-up
The Cardiac and Panvascular Medicine Diagnosis and Treatment Center, People's Hospital of Xinjiang Uygur Autonomous Region,
1 other identifier
observational
1,000,000
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2016
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2016
CompletedFirst Submitted
Initial submission to the registry
September 27, 2025
CompletedFirst Posted
Study publicly available on registry
October 6, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2035
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2035
October 6, 2025
September 1, 2025
20 years
September 27, 2025
September 27, 2025
Conditions
Outcome Measures
Primary Outcomes (16)
Mortality
All-cause and cause-specific mortality during follow-up
20 years
Cardiovascular diseases
Incident disease during follow-up
20 years
Digestive diseases
Incident disease during follow-up
20 years
Endocrine diseases
Incident disease during follow-up
20 years
Infections diseases
Incident disease during follow-up
20 years
Benign neoplasm or Carcinoma in situ
Incident disease during follow-up
20 years
Cancers
Incident disease during follow-up
20 years
Genitourinary diseases
Incident disease during follow-up
20 years
Haematological or immunological diseases
Incident disease during follow-up
20 years
Musculoskeletal diseases
Incident disease during follow-up
20 years
Neurological diseases
Incident disease during follow-up
20 years
Psychiatric diseases
Incident disease during follow-up
20 years
Respiratory diseases
Incident disease during follow-up
20 years
Ocular diseases
Incident disease during follow-up
20 years
Dermatological diseases
Incident disease during follow-up
20 years
Ear and mastoid disorders
Incident disease during follow-up
20 years
Eligibility Criteria
Eligible residents from routine annual health examinations.
You may qualify if:
- Residents \>=18y
- Permanent residents or individuals who have lived in the region for more than 5 years and are enrolled in local social security medical insurance
- Residents without severe physical disability and capable of normal communication
- Residents whose diseases and deaths are monitored and managed by the local health authorities
- Residents who voluntarily participate and provide written informed consent
You may not qualify if:
- Temporary residents or floating population
- Residents with severe health conditions that prevent participation in the study
- Residents who are unwilling to undergo follow-up assessments for the study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- People's Hospital of Xinjiang Uygur Autonomous Regionlead
- People's Hospital of Hotan Prefecturecollaborator
- People's Hospital of Altay Prefecturecollaborator
- Luopu County People's Hospital of Hotan Prefecturecollaborator
- The First People's Hospital of Aksu Prefecturecollaborator
- Karamay Central Hospital of Xinjiangcollaborator
- People's Hospital of Kizilsu Kyrgyz Autonomous Prefecturecollaborator
- The Second People's Hospital of Kashgar Prefecturecollaborator
- RenJi Hospitalcollaborator
Study Sites (1)
People's Hospital of Xinjiang Uygur Autonomous Region
Ürümqi, Xinjiang, 830001, China
Biospecimen
During routine health checkups, 10 mL of EDTA-anticoagulated blood, 10 mL of urine, 10 g of feces and 2 mL of saliva are collected. Samples are transported to the Biobank of the People's Hospital of Xinjiang Uygur Autonomous Region for processing within 2 hours and subsequently stored at -80 °C in an ultra-low temperature freezer.
Study Officials
- PRINCIPAL INVESTIGATOR
Yining Yang, Prof.
People's Hospital of Xinjiang Uygur Autonomous Region
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Prof.
Study Record Dates
First Submitted
September 27, 2025
First Posted
October 6, 2025
Study Start
January 1, 2016
Primary Completion (Estimated)
December 31, 2035
Study Completion (Estimated)
December 31, 2035
Last Updated
October 6, 2025
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will not share