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Following Chinese adults with overweight or obesity to track related health conditions

Follows adults in China with overweight or obesity for 3 years.

Plain-language title generated from the registry record
Registry title: Chinese Overweight/Obesity Cohort: Metabolic & Comorbidity Risks

Key facts

Where
Taiyuan, ChinaSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 79 years old?

Source: NCT07884903, who can take part

Where in China

  • Department of Endocrinology, Shanxi Bethune HospitalTaiyuan, ChinaNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Shanxi Bethune Hospital
Trial code
NCT07884903
Record updated
21 October 2026
Original description
This is a nationwide, multi-center, long-term follow-up study of overweight and obese adults in China. The study aims to recruit approximately 26,000 participants across 39 hospitals to better understand how body weight affects the development of obesity-related diseases over a 3-year period.Read full original descriptionShow less

A National Multicenter Prospective Cohort Study on the Incidence Characteristics and Risk Associations of Metabolic and Multi-system Comorbidities in Overweight and Obese Populations Stratified by Body Mass Index

This is a nationwide, multi-center, long-term follow-up study of overweight and obese adults in China. The study aims to recruit approximately 26,000 participants across 39 hospitals to better understand how body weight affects the development of obesity-related diseases over a 3-year period.

Eligible participants are adults aged 18 to 79 years with a body mass index (BMI) of 23 kg/m² or higher. Participants will be grouped into four categories based on their BMI: overweight, mild obesity, moderate obesity, and severe obesity.

At the beginning of the study, all participants will undergo a comprehensive health assessment, including physical measurements, body composition analysis, blood tests, and lifestyle questionnaires. Participants will then be followed for 3 years with annual check-ins to track any new health conditions.

The main goal is to identify the 3-year risk of developing conditions such as type 2 diabetes, fatty liver disease, high blood pressure, and heart disease in different weight groups. This information will help doctors better predict and prevent obesity-related health problems in the future.

Participation is voluntary, and all personal information will be kept confidential.

Inclusion: Adults aged 18 to 79 years; BMI ≥23.0 kg/m² (overweight or obese per 2026 ADA criteria); Able to provide written informed consent; Capable of completing baseline assessment and 3-year follow-up; Local residency for ≥3 years; Willing to provide fasting blood samples for storage.

Exclusion: Concurrent participation in other weight-loss or metabolic intervention trials; Secondary obesity (Cushing's syndrome, hypothyroidism, drug-induced or genetic obesity); End-stage severe chronic diseases (refractory heart failure, advanced malignancy, AIDS); Severe psychiatric disorders or cognitive impairment; Pregnancy or lactation.

ClinicalTrials.gov NCT07884903