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Determination of the Independent Effects of Beetroot Juice Components, Dietary Nitrate and Antioxidants, on Exercise Tolerance and Health Benefits in Individuals With Obesity

Determination of the Independent Effects of Beetroot Juice Components, Dietary Nitrate and Antioxidants, on Exercise Tolerance and Health Benefits in Individuals With Obesity

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03545009
Acronym
BEETIT
Enrollment
16
Registered
2018-06-04
Start date
2018-08-10
Completion date
2020-08-30
Last updated
2021-09-22

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

Conditions

Metabolic Disease, Obesity, Exercise

Brief summary

The purpose of this study is to assess the effects of acute beetroot juice supplementation on exercise performance and cardiometabolic health in obese individuals with secondary cardiometabolic complications. Additionally, we will determine if the ergogenic health benefits of beetroot juice is due to the nitric oxide compound within the product, the antioxidant compound within the product, or a combination of the two compounds.

Interventions

DIETARY_SUPPLEMENTSodium Nitrate

70ml sodium nitrate, matched for nitrate concentration in Beetroot Juice arm

DIETARY_SUPPLEMENTBeetroot Juice no Nitrate

70ml Concentrated Beetroot Juice with nitrate removed

DIETARY_SUPPLEMENTBeetroot Juice

70ml Concentrated Beetroot Juice

Sponsors

University of Alabama at Birmingham
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* BMI ≥ 30 kg/m2 * Able to perform exercise testing on a cycle ergometer

Exclusion criteria

* Currently taking medications know to affect cardiovascular or respiratory function * Currently supplementing with an antioxidant compound * Current smoker * Currently taking antibiotics * Not willing to abstain from mouthwash use * Currently participating in regular physical activity

Design outcomes

Primary

MeasureTime frame
Time to ExhaustionA Time to Exhaustion Test will be conducted on each participant a total of four times throughout their participation in the study. This will take place approximately 2.5 hours post ingestion of the dietary supplement they are randomized to at each visit.

Countries

United States

Outcome results

None listed

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