The Effect of Beetroot Juice on Muscle Strength and Muscle EMG Activity During Isokinetic Performance (NO Isokinetic)

Effects of Beetroot Juice Supplementation on Neuromuscular Activity and Isokinetic Strength and Power During Maximal Exercise

The primary aim of the current study is determine the effect of beetroot juice consumption on neuromuscular activation, isokinetic muscle strength and power

Study Overview

Detailed Description

Participants completed two experimental sessions in a randomized, double-blind, placebo-controlled crossover design separated by a minimum 3-day washout period. Prior to each session, participants were instructed to avoid nitrate-rich foods, strenuous exercise, antibacterial mouthwash, chewing gum, and tooth brushing.

All testing sessions were performed in the morning following an overnight fast. Upon arrival, anthropometric measurements were obtained and participants consumed either a nitrate-rich beetroot juice supplement (highNO) or nitrate-depleted placebo (lowNO). Following a standardized 2-hour absorption period, surface EMG electrodes were placed on the vastus medialis oblique (VMO) and vastus lateralis oblique (VLO) muscles according to SENIAM guidelines. Capillary blood samples were collected before exercise and 3 minutes after the fatigue protocol for blood lactate assessment.

Participants then completed a standardized 10-minute warm-up followed by isokinetic testing using a Biodex dynamometer. Testing was performed on the dominant lower limb at angular velocities of 180°/s, 60°/s, and 240°/s. Three maximal repetitions were performed at 60°/s and 180°/s, while a 30-repetition fatigue protocol was completed at 240°/s. Outcome measures included peak torque, peak power, total work, torque-angle variables, EMG activity, and blood lactate concentration.

Study Type

Interventional

Enrollment (Actual)

13

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Greater Poland Voivodeship
      • Poznan, Greater Poland Voivodeship, Poland, 61-871
        • Akademia Wychowania Fizycznego

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.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • age ≥18 years,
  • participation in at least three structured training sessions per week,
  • absence of musculoskeletal injuries within the previous 12 months

Exclusion Criteria:

  • smoking,
  • any injury within the past year

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Diagnostic
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Beetroot juice
beetroot juice with high concentration of nitrates ( 800mg)
acute dose of beetroot juice
Placebo Comparator: Depleted Beetroot Juice
beetroot juice with low concentration of nitrates
depleted nitrate beetroot juice

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The effect of beetroot juice ingestion on isokinetic strength
Time Frame: 2 hours
The aim of the present study was to examine the effects of acute ignestion of nitrate rich suplement compared with placebo on isokinetic muscle performance during knee extension and flexion tasks performed using an isokinetic dynamometer.
2 hours

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The effect of Beetroot Juice consumption on EMG muscle activity
Time Frame: 2 hours
Neuromuscular activity was assessed using surface electromyography of the vastus medialis oblique and vastus lateralis oblique muscles while Isokinetic tests
2 hours

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Robert Olek, Prof, Poznan University of Physical Education

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 Major Dates

Study Start (Actual)

May 15, 2025

Primary Completion (Actual)

May 15, 2025

Study Completion (Actual)

July 2, 2025

Study Registration Dates

First Submitted

May 18, 2026

First Submitted That Met QC Criteria

May 18, 2026

First Posted (Actual)

May 26, 2026

Study Record Updates

Last Update Posted (Actual)

May 26, 2026

Last Update Submitted That Met QC Criteria

May 18, 2026

Last Verified

May 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • RMPN2021/JJ3

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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