RECRUITING

The Effect of Beetroot Juice Supplementation Dose on Neuromuscular Performance During Resistance Exercise

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Dietary nitrate supplementation, administered in the form of nitrate-rich beetroot juice, has been shown to improve exercise performance and may have more pronounced effects on exercise that requires high-power and high-velocity muscle contraction such as weightlifting and body-mass resisted exercise (i.e, resistance exercise). However, limited data are available that have examined the potential performance enhancing effect of beetroot juice in resistance exercise. Moreover, there is no information on the dose of nitrate required for performance enhancing effects during resistance exercise which limits its widespread use to enhance performance. Therefore, the investigators will assess if supplementing the diet with nitrate-rich beetroot juice impacts resistance exercise performance (e.g., power, velocity), when compared to supplementing the diet with nitrate-depleted beetroot juice (i.e. placebo). The investigators will also investigate the dose-response effect of beetroot juice on resistance exercise performance by providing a low, moderate, and high nitrate dose of concentrated beetroot juice. The results of this study will improve understanding of whether beetroot juice influences resistance exercise performance and will provide insight on whether different doses of beetroot juice influence the efficacy of nitrate supplementation on resistance exercise performance. Together, these data will guide supplementation strategies for enhancing resistance exercise performance.

Official Title

The Effect of Beetroot Juice Supplementation Dose on Neuromuscular Performance During Resistance Exercise

Quick Facts

Study Start:2023-05-23
Study Completion:2024-06-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05957835

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 45 Years
Sexes Eligible for Study:MALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Recreationally active males who performed resistance exercise at least twice weekly for the last two years
  1. * individuals with contraindications to exercise, cardiometabolic disease, currently consuming dietary supplements containing caffeine, sodium bicarbonate, creatine, beta-alanine, and/or NO precursor supplements (i.e., NO3-, arginine, citrulline, antioxidants), females, and smokers

Contacts and Locations

Study Contact

Rachel Tan, PhD
CONTACT
3105067041
rachel.tan@pepperdine.edu
Adam Pennell, PhD
CONTACT
3105064162
adam.pennell@pepperdine.edu

Principal Investigator

Rachel Tan, PhD
PRINCIPAL_INVESTIGATOR
Pepperdine University

Study Locations (Sites)

Pepperdine University
Malibu, California, 90263
United States

Collaborators and Investigators

Sponsor: Pepperdine University

  • Rachel Tan, PhD, PRINCIPAL_INVESTIGATOR, Pepperdine University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-05-23
Study Completion Date2024-06-30

Study Record Updates

Study Start Date2023-05-23
Study Completion Date2024-06-30

Terms related to this study

Additional Relevant MeSH Terms

  • High Nitrate Dose
  • Moderate Nitrate Dose
  • Low Nitrate Dose
  • Nitrate-depleted Dose