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Effects of a High-fat Meal on Exercise-mediated Sympatholysis

Effects of a High-fat Meal on Exercise-mediated Sympatholysis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06186050
Enrollment
15
Registered
2023-12-29
Start date
2024-01-08
Completion date
2024-07-30
Last updated
2024-09-19

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

Conditions

Diet, Healthy

Keywords

Functional sympatholysis, Exercise

Brief summary

The goal of this trial is to examine the effects of a single high-fat meal with or without the co-ingestion of dietary nitrate on exercise-mediated sympatholysis. The main questions it aims to answer are: 1. What are the mechanisms responsible for reduced exercise-mediated sympatholysis following a high-fat meal 2. Can dietary nitrate prevent the declines in exercise-mediated sympatholysis Participants will be asked to complete three study visits in a randomized order: 1. Low-fat meal 2. High-fat meal 3. High-fat meal plus dietary nitrate Exercise-mediated sympatholysis will be measured using Doppler ultrasound via a protocol involving rhythmic handgrip exercise and a lower body negative pressure stimulus. Sympatholysis will be assessed before each meal, and at 1, 2, and 3 hours post-prandial.

Interventions

DIETARY_SUPPLEMENTBeetroot drink

Drink containing 10g of beetroot powder in 250 mL cold tap water

DIETARY_SUPPLEMENTPlacebo

Mio flavouring in 250 mL cold tap water. Trace amounts of sugar and sodium were added to match the content in the beetroot supplement

DIETARY_SUPPLEMENTControl

Low-fat meal with cornflakes, greek yogurt, skim milk, and orange juice

Sponsors

University of Guelph
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* 18-30 years of age * Healthy, free of known cardiovascular, metabolic, or musculoskeletal disease

Exclusion criteria

* Diagnosed cardiovascular or metabolic disease, injury preventing handgrip exercise, prescription of chronic medications other than oral contraceptives. * Inability to abstain from drugs (except oral contraceptives), caffeine, alcohol, strenuous physical activity, mouthwash, and multivitamins prior to study

Design outcomes

Primary

MeasureTime frameDescription
Forearm vascular conductanceBefore intervention and 1, 2, 3 hours post-interventionDuplex ultrasound of brachial artery
Forearm blood flowBefore intervention and 1, 2, 3 hours post-interventionDuplex ultrasound of brachial artery
Systolic and Diastolic Blood PressureBefore intervention and 1, 2, 3 hours post-interventionfinger plethysmography

Secondary

MeasureTime frameDescription
Plasma levels of NorepinephrineBlood collected before intervention and 1, 2, 3 hours post-intervention. Blood frozen at -80 degrees Celsius and analyzed at later dateELISA kit
Plasma levels of TriglyceridesBlood collected before intervention and 1, 2, 3 hours post-intervention. Blood frozen at -80 degrees Celsius and analyzed at later dateTriglyceride assay kit
Plasma levels of Nitrate/Nitrite concentrationBlood collected before intervention and 1, 2, 3 hours post-intervention. Blood frozen at -80 degrees Celsius and analyzed at later dateELISA kit
Blood Glucose concentrationsBlood collected before intervention and 1, 2, 3 hours post-intervention. Blood analyzed immediately after collection at each time pointBlood glucose monitor

Countries

Canada

Outcome results

None listed

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