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Viome Nutritional Programs to Improve Clinical Outcomes for Metabolic Conditions

Metabolic Health Clinical Trial

Official title:
Testing the Efficacy of Viome-designed Condition-based Supplements and Viome Precision Supplements to Improve Clinical Outcomes for Metabolic Conditions

Clinical Trial Summary

US residents who have obesity and sign the informed consent form and are screened and enrolled for this study. Participants who are enrolled complete a survey upon enrollment and are randomized into one of three arms. This study is direct to participant and will not utilize clinical sites.

Clinical Trial Description

Participants who meet the eligibility criteria are randomized into any of the three arms including: the placebo arm, VIOME's condition-based supplements (VCS) arm or the VIOME Precision Nutrition Program (VPNP) arm. Placebo, Viome-designed condition-based supplements and Viome's Precision Nutrition Program include supplements and/or dietary recommendations towards improving the symptoms associated with metabolic wellness. The trial will last approximately 4 months for each participant. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05564273
Study type Interventional
Source Viome
Contact Mory Mehrtash
Phone (425) 300-6933
Email studies@viome.com
Status Recruiting
Phase N/A
Start date October 13, 2023
Completion date December 2024
View Details
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