Evaluating Metabolic Health in People Aged 18 to 60 by Nutrilite Metabolic Health Index

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-10-09

Study Completion Date

2026-05-10

Brief Summary

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The goal of this observational study is to evaluate Metabolic Health by fit analysis between calculated Nutrilite Metabolic Health Index and the result of Metabolomics analysis from blood plasma samples in healthy adult participants aged between 18 and 60 years. The main question it aims to answer:

\- Does the Nutrilite Metabolic Health Index fit well with the result of Metabolomics analysis from blood plasma samples?

200 eligible participants will be enrolled in a single center, one site visit will be made to finish a health questionnaire, a lifestyle questionnaire, a routine physical checkup. Blood samples will be collected for routine blood test (blood sugar, total triglycerides, total cholesterol, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, uric acid), and for Metabolomics testing.

Researchers will calculate the Nutrilite Metabolic Health Index based on participant data, and do the fit analysis against the result from Metabolomics analysis.

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Detailed Description

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Conditions

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Metabolic Abnormality Metabolic Disorders

Study Design

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Observational Model Type

OTHER

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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All participants

All participants enrolled will be asked to fill out the questionnaires, have physical checkup, and take blood samples, no interventions involved.

No Intervention: Observational Cohort

Intervention Type OTHER

No intervention involved, participants will fill out some questionnaires and blood samples will drawn for test and analysis.

Interventions

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No Intervention: Observational Cohort

No intervention involved, participants will fill out some questionnaires and blood samples will drawn for test and analysis.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Male and female volunteers, aged 18 to 60, regardless of gender;
* Not participating in other interventional clinical studies;
* Have a good understanding of the nature, purpose, benefits obtained, and possible risks and side effects of the study;
* Willing to comply with all trial requirements and procedures;
* Sign the informed consent form.

Exclusion Criteria

* In the treatment of gastrointestinal symptoms;
* Those who are lactose intolerant, allergic to fish and their products;
* Current suffering from other organic diseases affecting bowel function, such as history of gastrointestinal resection, colon or rectal cancer, inflammatory bowel disease, diabetes, hyperthyroidism or hypothyroidism, Hirschsprung's disease, scleroderma, anorexia nervosa, etc.;
* Diet control, exercise enhancement, or taking medications that control weight or affect appetite in the past 3 months;
* Volunteers have any of the following medical history or have been clinically diagnosed with the following diseases that may affect the evaluation of the test results: obvious gastrointestinal disorders, liver, kidney, endocrine, blood, respiratory and cardiovascular diseases;
* Current or past abuse of alcohol or other illicit drugs, supplements, or OTC prescriptions 3 / 11 Research content Collection of biological samples or information data Evaluation indicators Drugs may cause intestinal dysfunction or affect the evaluation of trial effects;
* Frequent use of drugs that may affect gastrointestinal function or immune system according to the investigator's judgment.

Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes