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Viome Precision Nutritional Programs to Improve Clinical Outcomes for Mental Health Disorders
Sponsor: Viome
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
Conditions
Interventions
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