RecruitingNot ApplicableNCT07219498

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


Sponsor

University of Minnesota

Enrollment

24 participants

Start Date

Feb 5, 2026

Study Type

INTERVENTIONAL

Conditions

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).


Eligibility

Min Age: 18 YearsMax Age: 30 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Lactobacillus casei and Placebo Capsule(s) for people with exercise-induced muscle damage and delayed onset muscle soreness (doms). The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 30 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIETARY_SUPPLEMENTLactobacillus casei

Probiohealth 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.


Locations(1)

University of Minnesota

Minneapolis, Minnesota, United States

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NCT07219498