NCT07207863

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,000,000

participants targeted

Target at P75+ for all trials

Timeline
117mo left

Started Jan 2016

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress52%
Jan 2016Dec 2035

Study Start

First participant enrolled

January 1, 2016

Completed
9.7 years until next milestone

First Submitted

Initial submission to the registry

September 27, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

October 6, 2025

Completed
10.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2035

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2035

Last Updated

October 6, 2025

Status Verified

September 1, 2025

Enrollment Period

20 years

First QC Date

September 27, 2025

Last Update Submit

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

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Study Sites (1)

People's Hospital of Xinjiang Uygur Autonomous Region

Ürümqi, Xinjiang, 830001, China

RECRUITING

Biospecimen

Retention: SAMPLES WITH DNA

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

  • Yining Yang, Prof.

    People's Hospital of Xinjiang Uygur Autonomous Region

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Qian Zhao, Dr.

CONTACT

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

Locations