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CompletedNCT06045845Updated Feb 2, 2024

Effects of Beet Juice and Diet in Female Rowers

An interventional study of Beet Juice and Placebo in Dietary Habits, Nitrates and Exercise, sponsored by University of Kansas Medical Center. Completed at 1 site in United States. Open to female participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-02-02.

Sponsored by University of Kansas Medical Center · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
15
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
Female
01

Study summary

The purpose of this study is to determine the effects of nitrate-rich beetroot juice supplementation on exercise performance in female rowers when accounting for habitual vegetable nitrate consumption.

Read the detailed description

The objective is to use a stratified block randomization, double-blind crossover trial to test rowing ergometer exercise performance after drinking a beetroot juice supplement and compare it to the same test after consuming a placebo (a nitrate-free version of the beetroot juice supplement) in a convenience sample of athletes from a single Division 1-A collegiate women's rowing team.

Before testing, the participants' habitual vegetable nitrate consumption will be assessed from their report of foods consumed in the past 24 hours. Estimates of dietary nitrate intake will be calculated from the quantity of vegetables consumed and used to determine whether dietary nitrate intake influences the efficacy of the beetroot juice supplement.

02

Conditions studied

  • Dietary Habits
  • Nitrates
  • Exercise

Keywords

  • dietary nitrate
  • beetroot juice
  • sex differences
  • exercise
  • performance
  • muscle
03

In context

Lead sponsor

University of Kansas Medical Center is the lead sponsor of 483 studies on the registry; 113 are open to participants now.

Of its 38 completed or terminated interventional studies of FDA-regulated products, 24 (63%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  • Healthy
  • Athletes currently on the university's rowing team

Exclusion criteria

Exclusion Criteria:

  • Injuries or medical conditions that prevent participation in their team's rowing training program
  • Diagnosis of stage 2 iron deficiency
  • Unable to consume beet juice for any reason
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Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
15 participants (actual)

Study arms

  • Experimental
    Standard Beet Juice First

    First Test: Beet Juice / Second Test: Placebo

    Dietary Supplement: Beet Juice · Dietary Supplement: Placebo

  • Experimental
    Placebo Beet Juice First

    First Test: Placebo / Second Test: Beet Juice

    Dietary Supplement: Beet Juice · Dietary Supplement: Placebo

Interventions

  • Dietary supplementBeet Juice

    70 milliliter (70mL) standard Beet Juice (Beet It Sport Shot) consumed 2.5 hours before exercise test

  • Dietary supplementPlacebo

    70mL placebo Beet Juice (Beet It Sport Shot with nitrate removed) consumed 2.5 hours before exercise test

06

What researchers measure

Primary outcomes

  1. Rowing Test Time

    Time (seconds) to complete 500-meter rowing time trial tests.

    Time frame: Recorded immediately upon completion of each of the 4 500-meter intervals during rowing time trial tests on day 7 and day 14.

  2. Rowing Test Perceived Exertion

    Rating of perceived exertion reported by participant during rowing time trial tests. The Borg Scale is used, in which participants choose a number between 6 ("Rest") and 20 ("Maximal Effort") to indicate their perceived exertion at the completion of each 500-meter segment.

    Time frame: Recorded immediately upon completion of each of the 4 500-meter intervals during rowing time trial tests on day 7 and day 14.

  3. Rowing Test Peak Heart Rate

    Maximum heart rate (beats per minute) during 500-meter rowing time trial tests. The Maximum is the single highest heart rate recorded during that 500-meter interval.

    Time frame: Recorded during each of the 4 500-meter intervals during rowing time trial tests on day 7 and day 14.

  4. Rowing Test Average Heart Rate

    Mean heart rate (beets per minute) during 500-meter rowing time trial tests.

    Time frame: Recorded during each of the 4 500-meter intervals during rowing time trial tests on day 7 and day 14.

  5. Rowing Test Peak Power Output

    Maximum power (watts) during 500-meter rowing time trial tests

    Time frame: Recorded during each of the 4 500-meter intervals during rowing time trial tests on day 7 and day 14.

  6. Rowing Test Average Power Output

    Mean power (watts) during 500-meter rowing time trial tests

    Time frame: Recorded during each of the 4 500-meter intervals during rowing time trial tests on day 7 and day 14.

  7. Dietary Nitrate Habitual Consumption Amount

    Mean vegetable nitrate consumption (mg/day) from two different self-administered 24-hour dietary recalls (ASA24).

    Time frame: Collected after each rowing time trial test for the preceding 24-hour period (day 6 and day 13). Means determined in post-testing analysis.

  8. Dietary Nitrate Habitual Consumption Category

    Categorization of Dietary Nitrate Habitual Consumption Amount. The median of all participants' Amounts will be determined to categorize each participant as "high" (above median) or "low (below median).

    Time frame: Collected after each rowing time trial test for the preceding 24-hour period (day 6 and day 13). Median and categories determined in post-testing analysis.

07

Study locations

1 site
  • University of Kansas Rowing Boathouse
    Lawrence, Kansas 66044, United States
08

References and documents

Individual participant data

Plan to share: No — Upon completion of the testing protocol, all data analysis will be conducted using only using the de-identified participant identification numbers. There is no plan to share individual participant data with other researchers.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 2, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06045845
Lead sponsor
University of Kansas Medical Center
Responsible party
Jessica Provost (Principal Investigator, Doctoral Candidate, Graduate Teaching Assistant, University of Kansas Medical Center) — Principal investigator
First posted
Sep 21, 2023
Start date
Oct 3, 2023
Primary completion
Nov 17, 2023
Completion
Dec 31, 2023
Last update
Feb 2, 2024

Study contacts

Jessica A Provost, MS
principal investigator · University of Kansas Medical Center

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jan 2024. You cannot join it, but the record below documents what was studied.

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