- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05567926
Acute Effects of Beetroot Juice on Isometric Knee Extension Strength, Explosive Strength and Local Muscular Endurance
October 17, 2022 updated by: Zala Jenko Praznikar, University of Primorska
Acute Effects of Beetroot Juice Ingestion on Isometric Knee Extension Strength, Explosive Strength and Local Muscular Endurance
This is a double-blind placebo-controlled cross-over trial that aims to determine the acute effect of beetroot juice ingestion on isometric knee extension strength, explosive strength and local muscular endurance.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The study aims to determine whether concentrated beetroot juice has an acute effect on isometric strength of the knee muscles and the rate of force development in knee extension, as well as endurance of the same muscle.
This will be a cross-over study.
20 subjects will be randomly selected to the experimental group or control group; after 1 week, participants will repeat the measurements in the other condition.
Subjects will consume 140 ml of beetroot juice extract 2.5 hours before the measurement or placebo (140 ml of blackcurrant juice with added appropriate amount of sugar to equalize the carbohydrate value and lemon juice fort the taste).
An isometric dynamometer will be used to measure the isometric strength of the knee extensors.
Investigators will quantify peak force, rate of force development, endurance of knee extensors at 50 % of the maximal force, and the force recovery after a fatiguing protocol.
Study Type
Interventional
Enrollment (Actual)
20
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
-
-
-
Izola, Slovenia, SI-6310
- University Of Primorska Faculty of Health Sciences
-
-
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
18 years to 30 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Age between 18 and 30 years
- Physically active and healthy athletes (recreational or professional)
Exclusion Criteria:
- Cardiovascular, pulmonary, metabolic, neurological diseases and musculoskeletal injuries
- Smokers
- Consumption of drugs such as antacids and proton pump inhibitors in the previous 3 months
- Pregnant or breastfeeding women
- Beetroot allergic participants
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: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental condition, receiving beetroot juice supplement
Participants will receive beetroot juice intervention in the experimental condition.
|
A beetroot juice concentrate (140 ml) will be administered to participants in experimental conditions.
|
|
Placebo Comparator: Placebo condition
Participants will receive placebo (blackcurrant juice) in the placebo condition
|
140 ml of blackcurrant juice with added appropriate amount of sugar to equalize the carbohydrate value and lemon juice fort the taste.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knee extension strength
Time Frame: 2 hours after the ingestion of beetroot juice or placebo
|
The peak force during maximal voluntary contraction of knee extensors
|
2 hours after the ingestion of beetroot juice or placebo
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knee extension explosive strength
Time Frame: 2 hours after the ingestion of beetroot juice or placebo
|
The rate of force development during maximal voluntary contraction of knee extensors
|
2 hours after the ingestion of beetroot juice or placebo
|
|
Knee extension local muscle endurance
Time Frame: 2 hours after the ingestion of beetroot juice or placebo
|
Time to failure of knee muscles at 50 % of maximal force
|
2 hours after the ingestion of beetroot juice or placebo
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
October 1, 2022
Primary Completion (Actual)
October 15, 2022
Study Completion (Actual)
October 17, 2022
Study Registration Dates
First Submitted
October 2, 2022
First Submitted That Met QC Criteria
October 2, 2022
First Posted (Actual)
October 5, 2022
Study Record Updates
Last Update Posted (Actual)
October 19, 2022
Last Update Submitted That Met QC Criteria
October 17, 2022
Last Verified
October 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- BEETROOT
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
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.
Clinical Trials on Healthy Adults
-
Aix Marseille UniversitéNot yet recruitingHealthy Young Adults | Healthy Older AdultsFrance
-
PfizerNot yet recruitingHealthy | Healthy AdultsUnited States
-
Fundacion Clinic per a la Recerca BiomédicaNot yet recruitingHealthy Adult Participants | Non-smoking, Healthy Adults | Normal Weight AdultsSpain
-
KU LeuvenCompletedHealthy Older Adults | Ill Older AdultsBelgium
-
Samsung Medical CenterTerminatedHealthy Aging | Healthy AdultsKorea, Republic of
-
King Abdulaziz UniversityUniversity College Dublin; Royal College of Surgeons, IrelandRecruitingHealthy Adults | Healthy NutritionSaudi Arabia
-
Balgrist University HospitalNot yet recruiting
-
Essilor InternationalRecruiting
-
University of PennsylvaniaNational Institute on Aging (NIA)Not yet recruiting
-
MinicircleRecruiting
Clinical Trials on Beetroot juice concentrate (140 ml)
-
Poznan University of Physical EducationEnrolling by invitation
-
Queen Mary University of LondonCompletedCardiovascular DiseasesUnited Kingdom
-
Queen Mary University of LondonActive, not recruitingCardiovascular Diseases | Endothelial DysfunctionUnited Kingdom
-
University of VirginiaNot yet recruitingCoronary Microvascular Dysfunction (CMD) | Angina Patients With Non-obstructive Coronary Artery DiseaseUnited States
-
Oxford Brookes UniversityNot yet recruitingHypertension | Type 2 Diabetes Mellitus | Autonomic Nervous System DiseasesUnited Kingdom
-
Colorado State UniversityUnited States Department of Agriculture (USDA)UnknownObesity | Overweight | Menopause | AgingUnited States
-
University of CoimbraRecruitingDiabete Mellitus | Small Vessel Cerebrovascular DiseasePortugal
-
Bangor UniversityCompleted
-
Western Norway University of Applied SciencesCompleted
-
Universidad Francisco de VitoriaUniversity of Alcala; University of SevilleCompleted