Cohort StudyNCT07207863
Tianshan Community Cohort Establishment and Follow-up
An observational study of Cohort Study and Natural Population, run by People's Hospital of Xinjiang Uygur Autonomous Region at 1 site in China.
Trial 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. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Cohort Study, Natural Population, Northwest Region of China
- How many people
- 1,000,000 participants
- Where
- 1 siteChina
- Study dates
- 1 Jan 2016to 31 Dec 2035
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: Eligible residents from routine annual health examinations.
Who may be able to join
- 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
Who cannot join
- 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
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
China1 site, 1 recruiting
- Recruiting
People's Hospital of Xinjiang Uygur Autonomous Region
Ürümqi, Xinjiang, 830001
Qian Zhao, Dr., +8613899993630, tina0627@126.com
Yining Yang, Prof.
About this study
Official title: The Cardiac and Panvascular Medicine Diagnosis and Treatment Center, People's Hospital of Xinjiang Uygur Autonomous Region,
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.
Read the detailed description
This research is conducted through population-based health examinations among residents in northwest China. By providing annual health assessments, structured health education, and community-based health promotion activities, the study aims to enhance health awareness, identify determinants of disease, implement targeted interventions to improve lifestyle behaviors, reduce modifiable risk factors, and promote overall community health.
The cohort integrates data from multiple sources- including health assessments, electronic health records, mortality registries, statistical yearbooks, and environmental datasets- encompassing a wide range of health-related information, such as demographics, lifestyle factors, family and personal medical histories, living conditions, enrollment in national public health services, physical examinations, laboratory tests, diagnostic assessments, disease outcomes, and cause-specific mortality. Event-driven follow-up data are obtained from 163 hospitals and 63 Traditional Chinese Medicine hospitals, covering all secondary and tertiary-level hospitals in the region. Inpatient data are systematically documented by qualified medical personnel and entered into an electronic health information system. All disease diagnoses are coded according to the 10th Revision of the International Classification of Diseases (ICD-10). Mortality data, including the timing and specific cause of death, are primarily obtained through local death registration systems.
- Conditions
- Cohort Study, Natural Population, Northwest Region of China
What is being measured
The primary outcome is the main question the study is designed to answer.
Mortality
All-cause and cause-specific mortality during follow-up
Measured: 20 years
Cardiovascular diseases
Incident disease during follow-up
Measured: 20 years
Digestive diseases
Incident disease during follow-up
Measured: 20 years
Endocrine diseases
Incident disease during follow-up
Measured: 20 years
Infections diseases
Incident disease during follow-up
Measured: 20 years
Benign neoplasm or Carcinoma in situ
Incident disease during follow-up
Measured: 20 years
Cancers
Incident disease during follow-up
Measured: 20 years
Genitourinary diseases
Incident disease during follow-up
Measured: 20 years
Haematological or immunological diseases
Incident disease during follow-up
Measured: 20 years
Musculoskeletal diseases
Incident disease during follow-up
Measured: 20 years
Neurological diseases
Incident disease during follow-up
Measured: 20 years
Psychiatric diseases
Incident disease during follow-up
Measured: 20 years
Respiratory diseases
Incident disease during follow-up
Measured: 20 years
Ocular diseases
Incident disease during follow-up
Measured: 20 years
Dermatological diseases
Incident disease during follow-up
Measured: 20 years
Ear and mastoid disorders
Incident disease during follow-up
Measured: 20 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Oct 2025
- Study start1 Jan 2016
- Primary completion31 Dec 2035 (estimated)
- Study completion31 Dec 2035 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cohort StudyStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 1,000,000 participants (estimated)
Sponsor and investigators
- Lead sponsor
- People's Hospital of Xinjiang Uygur Autonomous Region
- Sponsor type
- University, hospital or other
- Collaborators
- People's Hospital of Hotan Prefecture, People's Hospital of Altay Prefecture, Luopu County People's Hospital of Hotan Prefecture, The First People's Hospital of Aksu Prefecture, Karamay Central Hospital of Xinjiang, People's Hospital of Kizilsu Kyrgyz Autonomous Prefecture, The Second People's Hospital of Kashgar Prefecture, RenJi Hospital
- Responsible party
- Principal investigator, Yining Yang, People's Hospital of Xinjiang Uygur Autonomous Region
- Investigators
- Yining Yang, Prof., Principal investigator, People's Hospital of Xinjiang Uygur Autonomous Region
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07207863
- Sponsor's protocol ID
- Tianshan2025
- Status last verified
- Sep 2025
- First submitted
- 27 Sep 2025
- Last updated
- 6 Oct 2025
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 6 Oct 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Cardiac and Panvascular Medicine Diagnosis and Treatment Center, People's Hospital of Xinjiang Uygur Autonomous Region,
- ClinicalTrials.gov ID
- NCT07207863
- Acronym / sponsor ID
- Tianshan2025
- Conditions
- Cohort Study, Natural Population, Northwest Region of China
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 1,000,000 participants (estimated)
- Lead sponsor
- People's Hospital of Xinjiang Uygur Autonomous RegionUniversity, hospital or other
- Collaborators
- People's Hospital of Hotan Prefecture, People's Hospital of Altay Prefecture, Luopu County People's Hospital of Hotan Prefecture, The First People's Hospital of Aksu Prefecture, Karamay Central Hospital of Xinjiang, People's Hospital of Kizilsu Kyrgyz Autonomous Prefecture, The Second People's Hospital of Kashgar Prefecture, RenJi Hospital
- Study start
- 1 Jan 2016 (actual)
- Primary completion
- 31 Dec 2035 (estimated)
- Study completion
- 31 Dec 2035 (estimated)
- First posted
- 6 Oct 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
This research is conducted through population-based health examinations among residents in northwest China. By providing annual health assessments, structured health education, and community-based health promotion activities, the study aims to enhance health awareness, identify determinants of disease, implement targeted interventions to improve lifestyle behaviors, reduce modifiable risk factors, and promote overall community health.
The cohort integrates data from multiple sources- including health assessments, electronic health records, mortality registries, statistical yearbooks, and environmental datasets- encompassing a wide range of health-related information, such as demographics, lifestyle factors, family and personal medical histories, living conditions, enrollment in national public health services, physical examinations, laboratory tests, diagnostic assessments, disease outcomes, and cause-specific mortality. Event-driven follow-up data are obtained from 163 hospitals and 63 Traditional Chinese Medicine hospitals, covering all secondary and tertiary-level hospitals in the region. Inpatient data are systematically documented by qualified medical personnel and entered into an electronic health information system. All disease diagnoses are coded according to the 10th Revision of the International Classification of Diseases (ICD-10). Mortality data, including the timing and specific cause of death, are primarily obtained through local death registration systems.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Eligible residents from routine annual health examinations.
Key inclusion criteria (5 listed)
- 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
Key exclusion criteria (3 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Mortality
Time frame: 20 years
All-cause and cause-specific mortality during follow-up
Cardiovascular diseases
Time frame: 20 years
Incident disease during follow-up
Digestive diseases
Time frame: 20 years
Incident disease during follow-up
Endocrine diseases
Time frame: 20 years
Incident disease during follow-up
Infections diseases
Time frame: 20 years
Incident disease during follow-up
Benign neoplasm or Carcinoma in situ
Time frame: 20 years
Incident disease during follow-up
Cancers
Time frame: 20 years
Incident disease during follow-up
Genitourinary diseases
Time frame: 20 years
Incident disease during follow-up
Haematological or immunological diseases
Time frame: 20 years
Incident disease during follow-up
Musculoskeletal diseases
Time frame: 20 years
Incident disease during follow-up
Neurological diseases
Time frame: 20 years
Incident disease during follow-up
Psychiatric diseases
Time frame: 20 years
Incident disease during follow-up
Respiratory diseases
Time frame: 20 years
Incident disease during follow-up
Ocular diseases
Time frame: 20 years
Incident disease during follow-up
Dermatological diseases
Time frame: 20 years
Incident disease during follow-up
Ear and mastoid disorders
Time frame: 20 years
Incident disease during follow-up
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Oct 2025.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Yining Yang, Prof. principal investigator
People's Hospital of Xinjiang Uygur Autonomous Region
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Cohort Study and Natural Population, run by People's Hospital of Xinjiang Uygur Autonomous Region at 1 site in China.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 6 Oct 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Qian Zhao, Dr. (+86-13899993630, tina0627@126.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Mortality (time frame: 20 years). The study lists 16 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Oct 2025.