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The Effect of Bovine Colostrum Supplementation in Older Adults

The Effect of Bovine Colostrum Supplementation in Older Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01792297
Enrollment
40
Registered
2013-02-15
Start date
2012-12-31
Completion date
2013-02-28
Last updated
2017-05-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sarcopenia, Osteoporosis

Keywords

Sarcopenia, Osteoporosis, Cognition, Inflammation

Brief summary

Bovine colostrum is the initial milk secreted by cows during the first day after calving. Colostrum is high in protein and contains a number of substances that have potential to be beneficial for the immune system. Preliminary studies about effects of colostrum supplementation show its potential for increasing human exercise performance; however, more evidence across the lifespan is required to confirm effects and to understand mechanisms of action. The objectives are to determine the effect of 8 weeks of bovine colostrum supplementation, compared to whey protein supplementation on the following dependent variables in men and women 50 years and older while participating in a resistance-training program: * muscle mass * strength * blood levels of growth factors and markers of inflammation * urine levels of muscle and bone catabolic markers * tests of cognitive ability It is hypothesized that bovine colostrum supplementation will result in greater increases in muscle mass, strength, blood IGF-1 levels (an anabolic hormone), and cognitive ability, and greater reductions in inflammation, and markers of muscle and bone catabolism, compared to placebo.

Interventions

DIETARY_SUPPLEMENTBovine colostrum
DIETARY_SUPPLEMENTWhey protein

Sponsors

Mitacs
CollaboratorINDUSTRY
University of Saskatchewan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Men or women 50 y or older

Exclusion criteria

* Milk allergies * Contraindications to exercise as indicated by the Physical Activity Readiness Questionnaire

Design outcomes

Primary

MeasureTime frameDescription
change from baseline in lean tissue mass at 8 weeksbaseline and 8 weeksLean tissue mass assessed by dual energy x-ray absorptiometry
Change from baseline in Upper body strength at 8 weeksbaseline and 8 weeksBench Press Strength
Change from baseline in Lower body strength at 8 weeksbaseline and 8 weeksLeg press strength

Secondary

MeasureTime frameDescription
Change from baseline in muscle catabolism at 8 weeksbaseline and 8 weeksUrinary 3-methylhistidine levels
Change from baseline in bone catabolism at 8 weeksBaseline and 8 weeksUrinary cross-linked N-telopeptides of type I collagen
Change from baseline in Insulin like growth factor-1 at 8 weeksbaseline and 8 weeksIGF-1 from serum
Change from baseline in inflammation at 8 weeksbaseline and 8 weeksSerum cytokine markers of inflammation (IL-6 and TNF-alpha)
Change from baseline in cognitive ability at 8 weeksbaseline and 8 weeksThe Telephone Interview of Cognitive Status
Number of Participants with Adverse Events as a Measure of Safety and Number of Participants with Adverse Events as a Measure of Safety and Tolerabilitycontinuously throughout 8 weeksAdverse events collected on adverse event forms
Change from baseline in upper body muscle thickness at 8 weeksbaseline and 8 weeksMuscle thickness of the elbow flexors assessed by ultrasound
Change from baseline in lower body muscle thickness at 8 weeksbaseline and 8 weeksKnee extensors muscle thickness assessed by ultrasound

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026