Post-exercise Blood Pressure With Inorganic Nitrate

Part of paid clinical trials in Charlottesville, Virginia.

Sponsor
University of Virginia
Study ID
NCT07869472
Status
Not Yet Recruiting

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Conditions

  • Central Adiposity
  • Obese Individuals

Eligibility Criteria

Sex
ALL
Age
18 Years - 40 Years
Healthy Volunteers
Accepted

Interventions

  • Beetroot Juice - Active + Exercise — DIETARY_SUPPLEMENT
    Supplement with 140 mL nitrate-rich beverage (800mg NO3-) (\~12.9 mmol/L) 1 hour 30 minutes before lab visit after a 3-day washout + ACUTE EXERCISE and post-exercise blood pressure, and central hemodynamics measured via impedance cardiography.
  • Beetroot juice placebo + Exercise — DIETARY_SUPPLEMENT
    Supplement with 140 mL nitrate-depleted beverage (\<0.1 mmol/L) after a 3-day washout + ACUTE EXERCISE, and post-exercise blood pressure, and central hemodynamics measured via impedance cardiography
  • Beetroot Juice - Active + No exercise — DIETARY_SUPPLEMENT
    Supplement with 140mL nitrate rich beverage (800mg NO3-) (\~12.9 mmol/L) 1 hour 30 minutes before lab visit after a 3 day washout + NO EXERCISE, and blood pressure, and central hemodynamics measured via impedance cardiography.
  • Beetroot juice placebo+ No exercise — DIETARY_SUPPLEMENT
    Supplement with 140 mL nitrate-depleted beverage (\<0.1 mmol/L) after a 3-day washout + NO EXERCISE, and blood pressure and central hemodynamics measured via impedance cardiography.

Study Details

This study is examining whether acute inorganic nitrate supplementation in the form of beetroot juice, paired with an acute bout of exercise, affects blood pressure and what is the magnitude of the difference compared to exercise alone.

Key Dates

First listed
Oct 9, 2026
Start date
Oct 15, 2026
Status verified
Oct 2026
Primary completion
Jan 1, 2027
Completion
Mar 30, 2027

Study Design

Enrollment
12 participants (estimated)
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER

Arms

  • Experimental: A
    1 x 4 crossover design where each participant will be randomized to complete four conditions after at least a 3-day washout period.
  • Active Comparator: B
    1 x 4 crossover design where each participant will be randomized to complete four conditions after at least a 3-day washout period.
  • Placebo Comparator: C
    1 x 4 crossover design where each participant will be randomized to complete four conditions after at least a 3-day washout period.
  • Sham Comparator: D
    1 x 4 crossover design where each participant will be randomized to complete four conditions after at least a 3-day washout period.

Primary Outcome Measure

Blood pressure (Central and Peripheral) [ Time Frame: Before each condition and after every 15 minutes for 3 hours. ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
University of VirginiaCharlottesvilleVirginia22903
Money Ghimire, M.S.
4349243004

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