Actively Recruiting

Phase Not Applicable
Age: 18Years - 30Years
All Genders
Healthy Volunteers
NCT07219498

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

Led by University of Minnesota · Updated on 2026-05-04

24

Participants Needed

1

Research Sites

47 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

Official Title

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

Who Can Participate

Age: 18Years - 30Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Complete at least 150 minutes per week of moderate intensity exercise (endurance or resistance training) based on self-reported activity in the past month
  • Be in good general health with no injuries or health conditions affecting physical activity
  • Willing to avoid regular use of NSAIDs and other probiotic supplements during the study
Not Eligible

You will not qualify if you...

  • Have known musculoskeletal injuries or physical limitations affecting required physical activity
  • Have health conditions increasing risk during exercise, such as cardiovascular, respiratory, or metabolic diseases
  • Currently taking probiotic supplements, prescribed antibiotics during the study, or using NSAIDs or steroids within the recovery window
  • Use NSAIDs more than twice per week regularly

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Minnesota

Minneapolis, Minnesota, United States, 55455

Actively Recruiting

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Research Team

J

Jakob Fischer

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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