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

Depression, Anxiety Clinical Trial

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

Clinical Trial 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.

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04905524
Study type Interventional
Source Viome
Contact
Status Completed
Phase N/A
Start date September 1, 2020
Completion date March 23, 2022
View Details
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