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RECRUITING
NCT06502717
NA

Viome Precision Nutritional Programs to Improve Clinical Outcomes for Mental Health Disorders

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 complete a survey upon enrollment and are randomized into one of two study 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

2024-07-08

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.

Locations (1)

Viome Life Sciences

Bothell, Washington, United States