NCT05766306

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

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

• Status: Completed
• Phase: Phase 2
• Study type: Interventional
• Enrollment: 30 (actual)
• Sponsor: Lallemand Health Solutions · Industry
• Sex: All
• Age: 13 Years – 17 Years
• Healthy volunteers: Accepted

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.

Detailed 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.

Conditions

• Stress

Interventions

Type	Name	Description
DIETARY_SUPPLEMENT	Probiotic Blend	Participants will be taking 1 sachet a day, 3 billion CFU.
DIETARY_SUPPLEMENT	Placebo	Participants will be taking 1 sachet a day.

Timeline

• Start date: 2023-03-15
• Primary completion: 2024-02-02
• Completion: 2024-02-02
• First posted: 2023-03-13
• Last updated: 2024-02-22

Locations

1 site across 1 country: Canada