NCT04987619

Brief Summary

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.

Trial Health

90
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
11

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jul 2021

Shorter than P25 for not_applicable

Geographic Reach
2 countries

6 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 5, 2021

Completed
15 days until next milestone

First Submitted

Initial submission to the registry

July 20, 2021

Completed
14 days until next milestone

First Posted

Study publicly available on registry

August 3, 2021

Completed
26 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 29, 2021

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 29, 2021

Completed
Last Updated

August 31, 2021

Status Verified

July 1, 2021

Enrollment Period

2 months

First QC Date

July 20, 2021

Last Update Submit

August 30, 2021

Conditions

Keywords

Explosive force productionBeetroot juiceBeetrootmuscular endurance

Outcome Measures

Primary Outcomes (1)

  • Change of height reached in jump

    Evaluated through CMJ (Counter movement jump) test with a recovery period of 45 seconds between jumps.

    Week 1, 2 and 3.

Secondary Outcomes (4)

  • Movement velocity

    Visit 1 (week 1), 2 (week 2) and 3 (week 3).

  • Power on back squat

    Visit 1 (week 1), 2 (week 2) and 3 (week 3).

  • Muscular endurance test

    Visit 1 (week 1), 2 (week 2) and 3 (week 3).

  • Rating of perceived exertion (RPE).

    Visit 1 (week 1), 2 (week 2) and 3 (week 3).

Study Arms (2)

BJR

EXPERIMENTAL

70 mL of beetroot juice (BEET It Sport®; James White Drinks Ltd., Ipswich, UK)

Dietary Supplement: Beetroot juice

PLA

PLACEBO COMPARATOR

70 mL of blackcurrant beverage Capri-Sun.

Other: Capri-Sun

Interventions

Beetroot juiceDIETARY_SUPPLEMENT

Subjects will drink juice 120 minutes before each visit

BJR

70 mL of blackcurrant beverage, which is depleted of NO3- will be taken 120 min before each visit.

PLA

Eligibility Criteria

Age18 Years - 30 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsGender identity
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (6)

Studies Research Group in Neuromuscular Responses (GEPREN), University of Lavras

Lavras, 37200-000, Brazil

Location

Maimonides Biomedical Research Institute of Cordoba (IMIBIC), Reina Sofia University Hospital, University of Cordoba

Córdoba, 14004, Spain

Location

Metabolism and Investigation Unit, Maimonides Biomedical Research Institute of Cordoba (IMIBIC),Reina Sofia University Hospital, University of Cordoba

Córdoba, 14004, Spain

Location

Department of Food Science and Technology, Rabanales University Campus, University of Cordoba

Córdoba, 14071, Spain

Location

Department of Nursing Pharmacology and Physiotherapy, Faculty of Medicine and Nursing, University of Córdoba

Córdoba, 14071, Spain

Location

Departamento de Motricidad Humana y Rendimiento Deportivo, Universidad de Sevilla

Seville, 41013, Spain

Location

Study Officials

  • Jose Manuel Jurado Castro

    Hospital Universitario Reina Sofía

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Masking Details
The order in which the participants will consume one supplement or another will be assigned randomly and double blind by an external collaborator to the research team, who will be responsible for coding the bottles.
Purpose
OTHER
Intervention Model
CROSSOVER
Model Details: The experimental procedure will consist of three visits, separate from each other by one week, to achieve the total elimination of any effects caused by BJR as well as the optimal recovery of the participants.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 20, 2021

First Posted

August 3, 2021

Study Start

July 5, 2021

Primary Completion

August 29, 2021

Study Completion

August 29, 2021

Last Updated

August 31, 2021

Record last verified: 2021-07

Data Sharing

IPD Sharing
Will share

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

Time Frame
After results are published
Access Criteria
Upon request to study's principal investigator

Locations