Actively Recruiting
Efficacy of Viome's Precision Nutrition Program Towards Reducing HbA1c
Led by Viome · Updated on 2025-01-29
100
Participants Needed
1
Research Sites
154 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is a randomized, placebo-controlled trial that will test the efficacy of VPNP in reducing HbA1c. Participant recruitment will occur through direct-to-participant enrollment. No additional clinical sites will be used for recruitment.
CONDITIONS
Official Title
Efficacy of Viome's Precision Nutrition Program Towards Reducing HbA1c
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Signed and dated informed consent form and medical release before any trial procedures
- Females and males aged 18 years or older
- Able to speak and read English
- HbA1c between 6.5% and 8.9%, tested within the past 30 days
- Willing and able to visit a Quest Diagnostic Patient Service Center
- Willing and able to follow the trial instructions and Viome's Precision Nutrition Program
- Willing and able to use a smartphone and Viome app
You will not qualify if you...
- Antibiotic use within one month before the GI test
- Pregnancy within the previous 6 months
- Current or previous use of medications that increase insulin (such as sulfonylureas)
- Current or previous use of exogenous insulin (such as Tresiba, Lantus, Toujeo, Levemir, Humalog, Novolog, Apidra, Fiasp)
- Following a specific diet like ketogenic to reduce HbA1c or weight within the previous month
- Taking diet pills
- Allergy to an ingredient in the MH capsule or stick pack
- Currently using an investigational product
- Significant surgery or medical procedure planned
- Diet or lifestyle changes during the trial period, except those appropriate for the trial arm
- Has already followed Viome nutritional recommendations (foods and/or supplements)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Viome Life Sciences
Bothell, Washington, United States, 98011
Actively Recruiting
Research Team
M
Mory Mehrtash
CONTACT
M
Momchilo Vuyisich
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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