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Avenanthramides and Exercise

Effect of Avenanthramides Supplement on Exercise-induced Physiological and Psychological Changes

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02584946
Enrollment
24
Registered
2015-10-23
Start date
2016-03-02
Completion date
2016-07-05
Last updated
2021-03-10

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

Conditions

Avenanthramides

Brief summary

The aim of the proposed study is to examine whether long-term dietary supplementation (8 weeks) of an oat flour cookie rich in avenanthramides (AVA) could enhance blood antioxidant capacity and reduce blood inflammatory markers after a downhill running (DR) protocol among human subjects.

Interventions

AVAs are a group of diphenolic acids that are found only in oats (Avena sativa).

Sponsors

PepsiCo Global R&D
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
20 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

1\. Male and female non-obese subjects (18kg/M2\<BMI\<28kg/M2) (age 20-45 years) will be recruited from the Twin Cities community. All participants will sign informed consent approved by UMN-IRB and are willing to avoid oat consumption and rigorous physical activity the day prior to and through test and to consume a low-polyphenol diet for 1 week prior to the study. The foods rich in polyphenols include all berries, apples, pears, citrus fruits, fruit juices, onions, chocolate, wine, coffee, tea, beans, nuts, soy products and most spices

Exclusion criteria

1. Presence of GI conditions that interfere with absorption; 2. Clinically significant endocrine, cardiovascular, pulmonary, renal, hepatic, pancreatic, biliary or neurologic disorders; 3. Major trauma or surgery within 3 months of visit; 4. Cancer in the prior 2 years; 5. Allergic to oat products; 6. Women who are pregnant or lactating; 7. Smoking; 8. Drinking alcohol \>5 drinks/week; 9. Using nutraceuticals; 10. Blood pressure medication; 11. NSAID (\>800 mg ibuprofen/week) 12. Vitamin supplementation 13. Anticoagulants or hypoglycemic drugs 14. Oat products consumption and rigorous physical activity the day before the test and consumption of a high-polyphenol diet in week prior to the test. 15. Moderate-intensity cardiorespiratory exercise training for ≥30 min•d-1 on ≥5 d•wk-1 for a total of ≥150 min•wk-1, vigorous-intensity cardiorespiratory exercise training for ≥20 min•d-1 on ≥3 d•wk-1 (≥75 min•wk-1), or a combination of moderate- and vigorous-intensity exercise to achieve a total energy expenditure of ≥500-1000 MET•min•wk-1

Design outcomes

Primary

MeasureTime frame
Mean and SD of plasma concentrations of Creatine Kinase0-72 hours

Secondary

MeasureTime frame
Mean and SD of plasma concentrations of TNF-α0-72 hours
Mean and SD of plasma concentrations of IL-60-72 hours
Mean and SD of plasma concentrations of ICAM-1, VCAM-1, NF-κB (P65), NRB, NF-κB binding to DNA, 4-Hydroxynenenol, F2-isoprostane0-72 hours

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026