Decentralized Study to Evaluate a Dietary Supplement for Episodes of Mild Acute Stress in Healthy People
NCT07511088
This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .
Summary
The purpose of this decentralized, two-arm, double-blinded, crossover clinical study is to test the efficacy of a supplement to reduce symptoms of acute stress or situational anxiety in healthy volunteers. The main questions it aims to answer are: Does a dietary supplement reduce feelings of anxiety after self-identified episodes of stress or anxiety when compared to their experience after taking a placebo? On a scale of 1-5, how much would the volunteer like to take the assigned treatment in the future? Are any adverse events identified after either treatment, supplement, or placebo?
Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov
Conditions studied
- Situational Anxiety
Eligibility basics and study details
- Study type
- Interventional
- Phase
- Not applicable
- Ages
- 18 to 60 years
- Sex
- All
- Healthy volunteers
- Accepted
- Sponsor
- PLT Health Solutions
- Last updated on ClinicalTrials.gov
- April 6, 2026
These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.
US recruiting sites
California · 1
- Alethios (Virtual) · San Francisco, CA
Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.