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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06073275
Other study ID # CDSJD
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 1, 2018
Est. completion date February 26, 2019

Study information

Verified date October 2023
Source Campus docent Sant Joan de Déu-Universitat de Barcelona
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study was a randomized, double-blind, crossover design for 3 weeks. In the first week, a researcher explained all the experimental procedures to the participants. In the following two weeks, the participants attended the Exercise Physiology laboratory to be assessed in 2 rowing ergometer sessions, separated from each other by a washout period of 7 days, under the same environmental conditions. In both strictly identical sessions, the participants randomly ingested beetroot juice (BRJ) or placebo (PL) 3 hours before the start of the tests.


Description:

Three hours after BRJ or PL intake, the participants began the 2,000-meter rowing ergometer test. Before starting (pretest) and at the end of the tests (posttest), blood oxygen saturation, rating of perceived exertion (RPE), and blood lactate measurements were taken. During the rowing ergometer tests, performance parameters and cardiorespiratory variables were recorded.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date February 26, 2019
Est. primary completion date January 31, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 30 Years and older
Eligibility Inclusion Criteria: 1. national and/or international level; 2. without cardiovascular, respiratory, metabolic, neurological or orthopedic disorders that may affect the performance of the rowing ergometer test; 3. no consumption of drugs or medicines; 4. no smoking; 5. Informed consent to participate in the study signed by all rowers Exclusion Criteria: 1. Ingestion of nutritional supplements taken in the three months prior to the start of the study; 2. no following the guidelines established by the nutrition professional.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Beetroot juice ingestion
Beetroot juice ingestion was randomly administered 3 h before the start of the test to the participants in two assessment sessions with a one-week washout between both sessions.
Placebo ingestion
Placebo ingestion was randomly administered 3 h before the start of the test to the participants in two assessment sessions with a one-week washout between both sessions.

Locations

Country Name City State
Spain Campus Docent Sant Joan de Déu. Universitat de Barcelona Sant Boi De Llobregat Barcelona

Sponsors (1)

Lead Sponsor Collaborator
Campus docent Sant Joan de Déu-Universitat de Barcelona

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rowing performance: Time trial minutes:seconds (mm:ss) through study completion, an average of 3 weeks
Primary Rowing performance: Mean Power output Watts through study completion, an average of 3 weeks
Primary Rowing performance: meter per stroke Meters through study completion, an average of 3 weeks
Primary Cardiorespiratory performance: absolute oxygen uptake V?O2max (L/min) through study completion, an average of 3 weeks
Primary Cardiorespiratory performance: relative oxygen uptake V?O2max (mL/kg/min) through study completion, an average of 3 weeks
Primary Cardiorespiratory performance: ventilatory efficiency slope of Ventilation/Carbon dioxide production through study completion, an average of 3 weeks
Primary Metabolic performance: lactate mmol/L through study completion, an average of 3 weeks
Secondary Cardiorespiratory performance: Maximum heart rate beats/min through study completion, an average of 3 weeks
Secondary Cardiorespiratory performance: Mean heart rate beats/min through study completion, an average of 3 weeks
Secondary Saturation percentage through study completion, an average of 3 weeks
Secondary Cardiorespiratory performance: minute ventilation minute ventilation in L/min through study completion, an average of 3 weeks
Secondary Scale of Perceived exertion ratio (RPE) Scale from 0 to 10. 0 = rest; 10 = maximum effort through study completion, an average of 3 weeks
Secondary Rowing performance: strokes Mean strokes per minute through study completion, an average of 3 weeks