Viome Nutritional Programs to Improve Clinical Outcomes for Gastrointestinal Conditions
- Conditions
- Gastrointestinal Health
- Registration Number
- NCT05465629
- Lead Sponsor
- Viome
- Brief 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.
- Detailed 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.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 150
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Efficacy of VIOME Precision Nutrition Program (VPNP) ~4months Number of participants that show an improvement in GI health compared to baseline survey assessment.
Efficacy of VIOME's designed condition based supplements (VCS) ~4 months Number of participants that show an improvement in GI health compared to baseline survey assessment.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Viome Life Sciences
🇺🇸Bothell, Washington, United States
Viome Life Sciences🇺🇸Bothell, Washington, United StatesMomchilo Vuyisich, PhDContactMory Mehrtash, MSHSContact(425) 300-6933studies@viome.com