Status:

COMPLETED

Changes in Plasma Amino Acid Appearance After Adding Bacillus Coagulans GBI-30, 6086 to Milk Protein Concentrate

Lead Sponsor:

Lindenwood University

Collaborating Sponsors:

Increnovo, LLC

Conditions:

Protein Malabsorption

Eligibility:

FEMALE

50-70 years

Phase:

NA

Brief Summary

The purpose of this study is to examine the pattern of plasma amino acid appearance after a two-week daily regimen of milk protein concentrate supplementation with and without the addition of Bacillus...

Detailed Description

Once determined eligible and providing consent, participants will be assigned in a randomized, double-blind, crossover fashion to ingest a single daily 25-gram dose of a milk protein concentrate or a ...

Eligibility Criteria

Inclusion

  • All participants will be between the ages of 50-70 years
  • Completing at least 30 minutes of physical activity at minimum three days per week

Exclusion

  • As indicated on a medical history form they complete, any individual who is currently being treated for or diagnosed with a cardiac, respiratory, circulatory, musculoskeletal, metabolic, obesity (defined as body mass index \> 30 kg/m2), immune, autoimmune, psychiatric, hematological, neurological or endocrinological disorder or disease
  • Any woman who is taking a medication known to impact digestive function or hormonal functions that may impact how our body digests, absorbs, or metabolizes nutrients
  • Any woman currently taking a probiotic or a dietary supplement that may impact digestive function or hormonal functions that may impact how our body digests, absorbs, or metabolizes nutrients
  • 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 overnight (8-10 hours)
  • Participants who do not or are not willing to abstain from exercise for 24 hours prior to each visit
  • Women who are pregnant
  • Women who are lactose intolerant

Key Trial Info

Start Date :

November 20 2020

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

February 1 2022

Estimated Enrollment :

30 Patients enrolled

Trial Details

Trial ID

NCT05313178

Start Date

November 20 2020

End Date

February 1 2022

Last Update

October 17 2024

Active Locations (1)

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Lindenwood University

Saint Charles, Missouri, United States, 63301