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
1 other identifier
interventional
11
2 countries
6
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jul 2021
Shorter than P25 for not_applicable
6 active sites
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
CompletedFirst Submitted
Initial submission to the registry
July 20, 2021
CompletedFirst Posted
Study publicly available on registry
August 3, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 29, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
August 29, 2021
CompletedAugust 31, 2021
July 1, 2021
2 months
July 20, 2021
August 30, 2021
Conditions
Keywords
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
EXPERIMENTAL70 mL of beetroot juice (BEET It Sport®; James White Drinks Ltd., Ipswich, UK)
PLA
PLACEBO COMPARATOR70 mL of blackcurrant beverage Capri-Sun.
Interventions
70 mL of blackcurrant beverage, which is depleted of NO3- will be taken 120 min before each visit.
Eligibility Criteria
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
Maimonides Biomedical Research Institute of Cordoba (IMIBIC), Reina Sofia University Hospital, University of Cordoba
Córdoba, 14004, Spain
Metabolism and Investigation Unit, Maimonides Biomedical Research Institute of Cordoba (IMIBIC),Reina Sofia University Hospital, University of Cordoba
Córdoba, 14004, Spain
Department of Food Science and Technology, Rabanales University Campus, University of Cordoba
Córdoba, 14071, Spain
Department of Nursing Pharmacology and Physiotherapy, Faculty of Medicine and Nursing, University of Córdoba
Córdoba, 14071, Spain
Departamento de Motricidad Humana y Rendimiento Deportivo, Universidad de Sevilla
Seville, 41013, Spain
Study Officials
- PRINCIPAL INVESTIGATOR
Jose Manuel Jurado Castro
Hospital Universitario Reina Sofía
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
- 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
- Time Frame
- After results are published
- Access Criteria
- Upon request to study's principal investigator
Data will be shared after the study concludes and results are published