Clinical Trials Directory

Trials / Completed

CompletedNCT04905524

Activity Changes in Irritable Bowel Syndrome (IBS), Anxiety, and Depression Following the Use of Viome Precision Nutrition Program (VPNP)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
10,000 (actual)
Sponsor
Viome · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Viome costumers are consented and recruited for this study and complete the questionnaires upon enrollment. Any participant who previously self reported depression, anxiety, or Irritable Bowel Syndrome (IBS) qualify for this study. All participants receive Viome's diet, supplement and recommendations.

Detailed description

Participants receive Viome Precision Nutrition Program (VPNP) after completing the health assessment and questionnaire. VPNP consists of diet, supplement and recommendations based on results from their sample results and their self reported questionnaire. After approximately 5 months, participants were given the same health assessment questionnaire. The results and data collected before and after the VPNP are analyzed to find correlations and differences between the measurements taken at the beginning of the trial and again approximately 5 months after.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTVIOME Precision Nutrition ProgramDiet and supplements recommendations

Timeline

Start date
2020-09-01
Primary completion
2022-03-23
Completion
2022-03-23
First posted
2021-05-27
Last updated
2022-04-04

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04905524. Inclusion in this directory is not an endorsement.