Effect of Beetroot Juice Supplements on Lower-limb Strength in Females

Acute Effects of Beetroot Juice Supplements on Lower-limb Strength and Muscular Endurance in Physically Active Women: Double-blind Crossover Randomized Trial

This study aims to evaluate the effects of beetroot juice supplements on lower-limb strength and muscular endurance in physically active women, due to the presence of NO3- in beetroot juice.

Study Overview

Status

Completed

Conditions

Detailed Description

Beetroot juice (BJR) is used as an ergogenic aid, but no study has analyzed its' effects on explosive force production in physically active women. It has been proposed that females could blunt reduction of NO2- to NO based on a higher oxidative skeletal muscle phenotype than males. However, it has been observed a higher increase on plasma NO2- levels after supplementation compared to and a greater enhancement on muscle contractile function.

Based on the absence of any study that has analyzed the effect of NO3- supplements on jump ability and power production on weightlifting on female population; the purpose of this study will be to investigate the possible ergogenic effect of BJR on physically active women on explosive force production and muscular endurance in a lower-limb body weightlifting protocol, due to the presence of NO3- in BJR and its effects.

Study Type

Interventional

Enrollment (Actual)

11

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

      • Lavras, Brazil, 37200-000
        • Studies Research Group in Neuromuscular Responses (GEPREN), University of Lavras
      • Córdoba, Spain, 14004
        • Maimonides Biomedical Research Institute of Cordoba (IMIBIC), Reina Sofia University Hospital, University of Cordoba
      • Córdoba, Spain, 14004
        • Metabolism and Investigation Unit, Maimonides Biomedical Research Institute of Cordoba (IMIBIC),Reina Sofia University Hospital, University of Cordoba
      • Córdoba, Spain, 14071
        • Department of Food Science and Technology, Rabanales University Campus, University of Cordoba
      • Córdoba, Spain, 14071
        • Department of Nursing Pharmacology and Physiotherapy, Faculty of Medicine and Nursing, University of Córdoba
      • Sevilla, Spain, 41013
        • Departamento de Motricidad Humana y Rendimiento Deportivo, Universidad de Sevilla

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

Yes

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Physically active females with 18-30 years of age
  • More than 6 months on RT training programs
  • Be familiarized with back squat, leg press and leg extension exercises
  • Not consuming any type of nutritional supplement or anabolic substances in the previous three months or during the study
  • Not suffering from a musculoskeletal injury that could interfere with the exercise protocol during the investigation

Exclusion Criteria:

  • None

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: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: BJR
70 mL of beetroot juice (BEET It Sport®; James White Drinks Ltd., Ipswich, UK)
Subjects will drink juice 120 minutes before each visit
Placebo Comparator: PLA
70 mL of blackcurrant beverage Capri-Sun.
70 mL of blackcurrant beverage, which is depleted of NO3- will be taken 120 min before each visit.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change of height reached in jump
Time Frame: Week 1, 2 and 3.
Evaluated through CMJ (Counter movement jump) test with a recovery period of 45 seconds between jumps.
Week 1, 2 and 3.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Movement velocity
Time Frame: Visit 1 (week 1), 2 (week 2) and 3 (week 3).
Evaluated at 50% and 75% repetition maximum (RM)
Visit 1 (week 1), 2 (week 2) and 3 (week 3).
Power on back squat
Time Frame: Visit 1 (week 1), 2 (week 2) and 3 (week 3).
Evaluated at 50% and 75% repetition maximum (RM)
Visit 1 (week 1), 2 (week 2) and 3 (week 3).
Muscular endurance test
Time Frame: Visit 1 (week 1), 2 (week 2) and 3 (week 3).
The test consists of three exercises: back squat, leg press and leg extension. Three series will be performed until concentric failure at 75% RM, three minutes of rest between each series.
Visit 1 (week 1), 2 (week 2) and 3 (week 3).
Rating of perceived exertion (RPE).
Time Frame: Visit 1 (week 1), 2 (week 2) and 3 (week 3).
Immediately at the end of the muscular endurance test, participants will be instructed to report their RPE using a scale 1-10 (worse to better outcome).
Visit 1 (week 1), 2 (week 2) and 3 (week 3).

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Jose Manuel Jurado Castro, Hospital Universitario Reina Sofia

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)

July 5, 2021

Primary Completion (Actual)

August 29, 2021

Study Completion (Actual)

August 29, 2021

Study Registration Dates

First Submitted

July 20, 2021

First Submitted That Met QC Criteria

August 2, 2021

First Posted (Actual)

August 3, 2021

Study Record Updates

Last Update Posted (Actual)

August 31, 2021

Last Update Submitted That Met QC Criteria

August 30, 2021

Last Verified

July 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • BEETROOT JUICE

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Data will be shared after the study concludes and results are published

IPD Sharing Time Frame

After results are published

IPD Sharing Access Criteria

Upon request to study's principal investigator

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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