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Clinical Trials/NCT03545009
NCT03545009CompletedNot Applicable

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

University of Alabama at Birmingham1 site in 1 country16 target enrollmentStarted: August 10, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
16
Locations
1
Primary Endpoint
Time to Exhaustion

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Basic Science
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 40 Years (Adult)
Sex
All
Accepts 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

Arms & Interventions

Beetroot Juice

Experimental

Intervention: Beetroot Juice (Dietary Supplement)

Beetroot Juice no Nitrate

Active Comparator

Intervention: Beetroot Juice no Nitrate (Dietary Supplement)

Control

No Intervention

Sodium Nitrate

Active Comparator

Intervention: Sodium Nitrate (Dietary Supplement)

Outcomes

Primary Outcomes

Time to Exhaustion

Time Frame: A 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.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Gordon Fisher

Associate Professor

University of Alabama at Birmingham

Study Sites (1)

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