Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING NA

Viome Precision Nutritional Programs to Improve Clinical Outcomes for Mental Health Disorders

NCT06502717 · View on ClinicalTrials.gov ↗

Study 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.

Interventions

  • COMBINATION_PRODUCT VIOME Precision Nutrition Program

Study Locations (1)

Washington

  • Viome Life Sciences — Bothell

Trial Details

FieldValue
Enrollment Target 150 participants
Start Date 2024-07-08
Est. Completion 2025-12
Phase NA

Sponsor

Viome

43 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06502717

The ClinicalTrials.gov registry entry for NCT06502717 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 150 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Viome, which has 43 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Depression appearing as the primary indexed condition, and to 1 intervention — of which VIOME Precision Nutrition Program is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06502717 reports 1 study location spanning 1 distinct geographic area — top geographies include Washington. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06502717 about?

NCT06502717 is a clinical study titled "Viome Precision Nutritional Programs to Improve Clinical Outcomes for Mental Health Disorders". 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.

What is the current status of trial NCT06502717?

This trial is currently recruiting. It is a NA study. The enrollment target is 150 participants. The study started on 2024-07-08. Estimated completion is 2025-12.

What conditions does trial NCT06502717 study?

This clinical trial studies the following conditions: Depression, Anxiety, Mental Health Issue. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06502717?

The interventions under investigation include: VIOME Precision Nutrition Program (COMBINATION_PRODUCT). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06502717?

This trial is sponsored by Viome, which has 43 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06502717 being conducted?

This trial has 1 study location across Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial