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ACTIVE NOT RECRUITING
NCT05563857
NA

Viome Nutritional Programs to Improve Clinical Outcomes for Mental Health Conditions

Sponsor: Viome

View on ClinicalTrials.gov

Summary

US residents who have mental health 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.

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

Key Details

Gender

All

Age Range

25 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

150

Start Date

2022-10-19

Completion Date

2025-12

Last Updated

2025-01-29

Healthy Volunteers

No

Interventions

COMBINATION_PRODUCT

VIOME Precision Nutrition Program

Precision supplement based on the participants microbiome sample results. Participants in this arm may have any combination of supplements, diet recommendations, and/or coaching.

DIETARY_SUPPLEMENT

VIOME-designed condition-based supplements

Pre-formulated supplements based on overall health conditions. Participants in this arm may have any combination of supplements, diet recommendations, and/or coaching.

Locations (1)

Viome Life Sciences

Bothell, Washington, United States