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Nutriomics and Artificial Intelligence Nutrition Obesity Cohort

Recruiting
Conditions
Obesity
Registration Number
NCT05494138
Lead Sponsor
Yonsei University
Brief Summary

The purpose of this study is to establish a prospective cohort. From registration to the 5th year, basic investigation, specific examinations for cardiovascular and metabolic disease, basic blood tests, collection of human material samples, and clinical event follow-up are conducted yearly. The obese group will be examined yearly, and telephone follow-up will be conducted if necessary. The control group will participate in the baseline survey once enrollment and clinical event follow-up by phone will be conducted annually thereafter. From the 6th year, only clinical event follow-up will be conducted.

Detailed Description

The obese group will enroll 500 people within 1 year of study initiation and follow-up annually. The control group will enroll 30 patients a year for 5 years.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
650
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Differences of nutriomics according to obesity phenotypesAt five years of study

Cross-sectional analysis of nutriomics of normal control group and obese patients

Secondary Outcome Measures
NameTimeMethod
Clinical eventsthree years, four years, five years, etc

A composite of all-cause mortality, cardiovascular mortality, non-fatal myocardial infarction, non-fatal stroke, revascularization of coronary artery, and heart failure hospitalization

Trial Locations

Locations (1)

Yonsei University Health System, Severance Hospital

🇰🇷

Seoul, Korea, Republic of

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