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The Efficacy of a Probiotic Blend on Stress in Moderately Stressed Teens — TEEN  

Stress Clinical Trial

Official title:
A Randomized, Double-blind, Placebo-controlled, Parallel Study Investigating the Efficacy of a Probiotic Blend on Stress in Adolescents With Moderate Perceived Stress

Clinical Trial Summary

The goal of this clinical trial is to test to efficacy of a probiotic blend on stress in adolescents with moderate perceived stress. It is hypothesized that those taking the probiotic blend will have decreased levels of stress compared to those receiving the placebo.

Clinical Trial Description

Participants in this randomized, double-blind, placebo-controlled, parallel study will be adolescents with moderate perceived stress. Participants will be enrolled in this study for 63 days, with a 56-day intervention period and a 7 day follow-up period. There will be a total of 5 visits: 4 in-person and 1 follow-up phone call. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05766306
Study type Interventional
Source Lallemand Health Solutions
Contact
Status Completed
Phase Phase 2
Start date March 15, 2023
Completion date February 2, 2024
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