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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | VIOME Precision Nutrition Program | Diet 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.