The Impact of Plant-based Blends on Skeletal Muscle Protein Synthesis Rates in Older Adults
NCT ID: NCT05917223
Last Updated: 2024-10-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
NA
48 participants
INTERVENTIONAL
2023-07-01
2025-05-31
Brief Summary
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Therefore, the purpose of this study is to investigate the effect of a higher-quality plant-based protein blend with lifting weight on muscle building in older men and women.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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Milk protein ingestion
Consuming 20 g of Milk Protein dissolved in 350mL of water, one time at the experiment visit
Milk protein ingestion
It's just an acute intervention, so the participant assigned to the Milk protein ingestion group will consume 20 g of milk protein during infusion protocol.
Corn protein ingestion
Consuming 20 g of Corn protein isolation dissolved in 350mL of water, one time at the experimental visit
Cron protein ingestion
It's just an acute intervention, so the participant assigned to the Corn protein ingestion group will consume 20 g of corn protein isolation during infusion protocol.
Corn+Pea protein ingestion
Consuming 20 g of Corn+Pea protein isolation dissolved in 350mL of water, one time at the experimental visit
Corn+Pea protein ingestion
It's just an acute intervention, so the participant assigned to the Corn+Pea protein ingestion group will consume 20 g of Corn+Pea protein isolation during infusion protocol.
Non-protein, low energy
Consuming 20 g of carbohydrate dissolved in 350mL of water, one time at the experimental visit
Non-protein, low energy
It's just an acute intervention, so the participant assigned to the Non-protein, low energy group will consume 20 g of carbohydrate during infusion protocol.
Interventions
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Milk protein ingestion
It's just an acute intervention, so the participant assigned to the Milk protein ingestion group will consume 20 g of milk protein during infusion protocol.
Cron protein ingestion
It's just an acute intervention, so the participant assigned to the Corn protein ingestion group will consume 20 g of corn protein isolation during infusion protocol.
Corn+Pea protein ingestion
It's just an acute intervention, so the participant assigned to the Corn+Pea protein ingestion group will consume 20 g of Corn+Pea protein isolation during infusion protocol.
Non-protein, low energy
It's just an acute intervention, so the participant assigned to the Non-protein, low energy group will consume 20 g of carbohydrate during infusion protocol.
Eligibility Criteria
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Inclusion Criteria
* Be in good general health
* Non-smoking
* Recreationally active but not meet Canada's Physical Activity Guidelines (150 min of moderate-intensity exercise/week)
* Have a body mass index (BMI) between 18.5-30 kg/m2 (inclusive)
* Willing and able to provide informed consent (speaks and understands English)
Exclusion Criteria
* Use assistive walking devices (e.g., cane or walker)
* Any concurrent medical, orthopedic, or psychiatric condition that, in the opinion of the investigator, would compromise his/her ability to comply with the study requirements
* History of cancer within the last 5 years, except basal cell carcinoma, non-squamous skin carcinoma, prostate cancer or carcinoma in situ with no significant progression over the past 2 years
* Significant orthopedic, cardiovascular, pulmonary, renal, liver, infectious disease, immune disorder, metabolic/endocrine, neuromuscular or bone wasting disorders
* Any cachexia-related condition (e.g., relating to cancer, tuberculosis or human immunodeficiency virus infection and acquired immune deficiency syndrome) or any genetic muscle diseases or disorders
* History of statin myalgia
* Current illnesses which could interfere with the study (e.g., prolonged severe diarrhea, regurgitation, difficulty swallowing)
* Excessive alcohol consumption (\>21 units/week)
* History of bleeding diathesis, platelet or coagulation disorders, or antiplatelet/anticoagulation therapy (up to 81mg of baby aspirin per day taken as a prophylactic is permitted).
* Routine/daily usage of non-steroidal anti-inflammatory drugs (NSAIDS, prescription use or daily use of over-the-counter medication), use of corticosteroids, testosterone replacement therapy (ingestion, injection, or transdermal), any anabolic steroid, creatine, whey protein supplements, casein or branched-chain amino acids (BCAAs) within 45 days prior to screening.
* A history of falls determined by a score \>25 on the Falls Efficacy Scale-International (FES-I).
60 Years
80 Years
ALL
Yes
Sponsors
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McMaster University
OTHER
Responsible Party
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Stuart Phillips
Professor
Principal Investigators
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Stuart Phillips, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
McMaster University
Locations
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Ivor Wynne Centre
Hamilton, Ontario, Canada
Countries
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Other Identifiers
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16408
Identifier Type: -
Identifier Source: org_study_id
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