Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07219498

Effects of a 5-Week Probiotic Supplementation Intervention on Markers of Delayed Onset Muscle Soreness

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
24 (estimated)
Sponsor
University of Minnesota · Academic / Other
Sex
All
Age
18 Years – 30 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to evaluate how probiotic supplementation (PS) influences post-exercise recovery in healthy, physically active young adults. Researchers aim to determine if the Lactobacillus casei probiotic strain reduces symptoms of delayed onset muscle soreness (DOMS) based on perceived muscle soreness, pressure pain threshold, and power output following exercise induced muscle damage (EIMD).

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTLactobacillus caseiProbiohealth is the manufacturer of this strain and they use a stringent quality control program that utilizes a multi point product variability check system.
OTHERPlacebo Capsule(s)The brand name of placebo capsules that will be used in this study is Magic Bullet Placebo Capsules. This placebo is manufactured by Progressive Placebo as stated on the product label.

Timeline

Start date
2026-02-05
Primary completion
2026-04-30
Completion
2026-04-30
First posted
2025-10-22
Last updated
2026-02-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07219498. Inclusion in this directory is not an endorsement.