- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07605455
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
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Greater Poland Voivodeship
-
Poznan, Greater Poland Voivodeship, Poland, 61-871
- Akademia Wychowania Fizycznego
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
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
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
Investigators
- Principal Investigator: Robert Olek, Prof, Poznan University of Physical Education
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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