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_SUPPLEMENTSupplement 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_SUPPLEMENTSupplement 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_SUPPLEMENTSupplement 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_SUPPLEMENTSupplement 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: A1 x 4 crossover design where each participant will be randomized to complete four conditions after at least a 3-day washout period.
- Active Comparator: B1 x 4 crossover design where each participant will be randomized to complete four conditions after at least a 3-day washout period.
- Placebo Comparator: C1 x 4 crossover design where each participant will be randomized to complete four conditions after at least a 3-day washout period.
- Sham Comparator: D1 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
- Money Ghimire, M.S4349243004
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Virginia | Charlottesville | Virginia | 22903 |
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