Changes in Plasma Amino Acid Appearance After Adding Bacillus Coagulans GBI-30, 6086 to Milk Protein Concentrate
Completed · Not applicable
Conditions studied: Protein Malabsorption
In brief
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 coagulans GBI-30, 6086 among older women.
Key facts
- Study ID
- NCT05313178
- Run by
- Lindenwood University
- People needed
- 30
- Starts
- 2020-11-20
- Expected to finish
- 2022-02-01
- Last updated by the study team
- 2024-10-17
Who can join
Age: 50 and older, up to 70. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- 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
You may not qualify if…
- 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
Where it is running
- Lindenwood University — Saint Charles, Missouri, United States
Full record on ClinicalTrials.gov
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