Activity Changes in Irritable Bowel Syndrome (IBS), Anxiety, and Depression Following the Use of Viome Precision Nutrition Program (VPNP)
Status
Conditions
Treatments
Details and patient eligibility
About
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.
Full 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.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- PHQ-9 score 5 or above
- GAD-7 score 5 or above
- IBS ROME-IV score 125 or above
- Females and males aged 18 years or older
- Signed and dated informed consent prior to any trial-specific procedures are performed
- Able to speak and read English
- Willing and able to follow the trial instructions
- Viome existing costumer
Exclusion criteria
- Unable/unwilling to complete the provided questionnaires
Trial design
Primary purpose
Allocation
Interventional model
Masking
10,000 participants in 1 patient group
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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