A Population-based Cohort of Osteoarthritis: the Tsinghua University Tiantongyuan Community Osteoarthritis Study
1 other identifier
observational
4,000
1 country
1
Brief Summary
The purpose of this study is to examine the natural history and risk factors of osteoarthritis (OA) and to explore the relationship between metabolic factors and OA progression.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jun 2025
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
First Submitted
Initial submission to the registry
May 20, 2025
CompletedStudy Start
First participant enrolled
June 3, 2025
CompletedFirst Posted
Study publicly available on registry
June 5, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2034
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2034
June 5, 2025
May 1, 2025
9.6 years
May 20, 2025
May 27, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Incidence of Osteoarthritis
The occurrence of clinically diagnosed osteoarthritis based on imaging and clinical symptoms during the follow-up period.
Annually for 10 years
Secondary Outcomes (13)
Change in Joint Pain Severity (WOMAC Pain Subscale)
Annually for 10 years
Change in Physical Function (WOMAC Subscale)
Annually for 10 years
Change in Physical Function (SF-36 Physical Function Domain)
Annually for 10 years
Timed Up and Go Test (TUGT)
Annually for 10 years
Five Times Sit-to-Stand Test (5TSTS)
Annually for 10 years
- +8 more secondary outcomes
Eligibility Criteria
This study will include adults aged 50 years and above to investigate osteoarthritis risk factors and progression in a general population-based cohort.
You may qualify if:
- Aged 50 years and above
- Long-term resident of the study area
- Willing to participate and provide informed consent
You may not qualify if:
- Hearing, speech, or mental impairments preventing effective communication
- Unable to complete scheduled follow-up visits
- Pregnant or planning pregnancy during the study period
- Any other condition deemed unsuitable for participation by the researchers
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Beijing Tsinghua Chang Gung Hospital
Beijing, Beijing Municipality, 102218, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 20, 2025
First Posted
June 5, 2025
Study Start
June 3, 2025
Primary Completion (Estimated)
December 31, 2034
Study Completion (Estimated)
December 31, 2034
Last Updated
June 5, 2025
Record last verified: 2025-05