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Viome Nutritional Programs to Improve Clinical Outcomes for Mental Health Conditions

Depression Clinical Trial

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

Clinical Trial Summary

US residents who have gastrointestinal issues 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 control 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, may include dietary recommendations towards improving the symptoms associated with gastrointestinal wellness. The trial will last approximately 4 months for each participant. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05563857
Study type Interventional
Source Viome
Contact
Status Active, not recruiting
Phase N/A
Start date October 19, 2022
Completion date December 2024
View Details
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