Status:

COMPLETED

Changes in Amino Acid Absorption After Adding a Probiotic to an Acute Protein Feeding

Lead Sponsor:

Lindenwood University

Conditions:

Amino Acid Absorption

Eligibility:

All Genders

18-50 years

Phase:

NA

Brief Summary

The purpose of this study is to examine the pharmacokinetic pattern of amino acid absorption after a two-week pattern of milk protein supplementation with and without the addition of Bacillus coagulan...

Detailed Description

The study will be conducted using a randomized, double-blind, crossover study design. 30 healthy men and women between the ages of 18 - 55 years of age will be recruited to participate in this study. ...

Eligibility Criteria

Inclusion

  • All participants will be between the ages of 18-55 years.
  • Participants will be healthy and free of disease as determined by evaluation of a medical history.
  • Completing at least 30 minutes of moderate exercise three days per week

Exclusion

  • Those individuals less than 18 and greater than 55 years of age will be excluded.
  • Any individual who is currently being treated for or diagnosed with a cardiac disorder or disease
  • Any individual who is currently being treated for or diagnosed with a respiratory disorder or disease
  • Any individual who is currently being treated for or diagnosed with a circulatory disorder or disease
  • Any individual who is currently being treated for or diagnosed with a musculoskeletal disorder or disease
  • Any individual who is currently being treated for or diagnosed with a metabolic disorder or disease
  • Any individual who is currently being treated for or diagnosed with obesity (defined as body mass index \> 30 kg/m and body fat greater than 30%)
  • Any individual who is currently being treated for or diagnosed with an immune or autoimmune disorder or disease
  • Any individual who is currently being treated for or diagnosed with a psychiatric disorder or disease
  • Any individual who is currently being treated for or diagnosed with a hematological disorder or disease
  • Any individual who is currently being treated for or diagnosed with a neurological disorder or disease
  • Any individual who is currently being treated for or diagnosed with an endocrinological disorder or disease
  • Participants who are determined to not be weight stable defined as measured body mass deviating by 2% or more.
  • Participants who do not or are not willing to abstain from alcohol, nicotine, and caffeine for 12 hours prior to each visit will be excluded
  • Participants who do not or are not willing to abstain from exercise for 12 hours prior to each visit will be excluded.

Key Trial Info

Start Date :

August 8 2019

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 3 2019

Estimated Enrollment :

30 Patients enrolled

Trial Details

Trial ID

NCT04427020

Start Date

August 8 2019

End Date

December 3 2019

Last Update

June 11 2020

Active Locations (1)

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Lindenwood University

Saint Charles, Missouri, United States, 63301