Ignite Creation Date:
2024-10-26 @ 3:35 PM
Last Modification Date:
2024-10-26 @ 3:35 PM
Study NCT ID:
NCT06502717
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-06-25
Brief Title:
Viome Precision Nutritional Programs to Improve Clinical Outcomes for Mental Health Disorders
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Testing the Efficacy of Viome-designed Condition-based Supplements and Viome Precision Supplements to Improve Clinical Outcomes for Mental Health Conditions
Status:
RECRUITING
Status Verified Date:
2024-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
US residents who have mental health issues sign the informed consent form and are screened and enrolled for this study Participants complete a survey upon enrollment and are randomized into one of two study arms This study is direct to participant and will NOT utilize clinical sites
Detailed Description:
Participants who meet the eligibility criteria are randomized into any of the two study arms including the placebo arm or the VIOME Precision Nutrition Program VPNP arm
Placebo and Viomes Precision Nutrition Program include supplements may include dietary recommendations towards improving the symptoms associated with mental health The trial will last approximately 4 months for each participant
Placebo and Viomes Precision Nutrition Program include supplements may include dietary recommendations towards improving the symptoms associated with mental health The trial will last approximately 4 months for each participant
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None