The Effect of Coconut Water on Varsity Basketball Performance

April 6, 2018 updated by: Peter Lemon, Western University, Canada
This study will assess whether there is a performance enhancing effect associated with hydrating with coconut water. There have been only two studies in the past that have examined this phenomenon, however these studies have limitations due to their design parameters. Kalman et al. (2012) ".... while treadmill time to exhaustion is routinely used in laboratory studies, the use of a time trial test as the measure of exercise performance may be more appropriate." While Peart et al. (2016) stated: "limitations to the exercise protocol employed here may have contributed to the absence of a performance improvement with coconut water."

Study Overview

Detailed Description

Purpose The purpose of the study is to determine whether hydrating with coconut water during a game-simulated, basketball-specific training session can enhance performance. It is hypothesized that coconut water will provide an ergogenic effect for basketball players.

Sample The sample will include 20 varsity basketball players, male and female, ranging in age from 18-35 who volunteer to participate in the study. This sample size is justified assuming a standard deviation of 1.5 based on previous studies and using a power of 80% with the statistical significance of 0.05 the resulting n would be 2(1.5)^2*(0.84+1.96)^2/5=7 (Kadam, P., & Bhalerao, S. (2010). Sample size calculation. International journal of Ayurveda research, 1(1), 55). To account for dropouts, 10 participants will be recruited for each group. Participants will be required to have no history of kidney problems. All individuals must give written informed consent in order to participate in the study. Exclusion criteria include not being a varsity basketball player, being younger than 18 or older than 35, or having a history of kidney problems.

Procedure Inclusion/exclusion criteria will be explicitly stated throughout the recruitment process. Potential participants will be recruited through first contacting the Men's and Women's Head Basketball Coaches of Western University and obtaining approval of collaboration from the team. Players will then be in direct contact with Reed Zehr to gain information of study. After given the study details, individuals will be given up to 3 days to determine if they want to participate and give their informed consent. See attached form in the consent section of the ethics application.

Measurement: All players will perform two sessions of a 10 minute BSST (Basketball Specific Skills Test) which will represent the 1st and 2nd quarter respectively. Field Goal Attempts (FGA) (#), Field Goals Made (FGM) (#), Field Goal Percentage (FGP) (%) will be measured from the free-throw line, mid-range and three point distances during the BSST. A dribbling drill will be used as well and number of dribbles (#) will be measured. All players will then perform two sessions of a 10 minute BEST (Basketball Exercise Simulation Test) test which will represent the 3rd and 4th quarter of a basketball game. Total distance covered (m), Mean circuit completion time (s), mean sprint time (s), and total sprint decrement (%) will be measured during the BEST.

Protocol: On test days, participants will report to he Gym at 0600 h after a 12 h overnight fast and having abstained from any strenuous exercise following the evening meal. At 0615 h, participants will consume a standardized breakfast (toast and jam) and the first beverage of 750mL. At 0730 h, participants will be told to consume the second beverage of 250mL. At 0745 h, the participants will undergo the first 10 min quarter of the BSST. At 0755 h, the participants rest during a 2 min break (1st intermission) and consume the third beverage of 250mL. At 0757 h, the participants will undergo the second session of the BSST. At 0807 h, the participants receive a 15 min break (half-time) and consume the fourth beverage of 500mL. At 0822 h, the participants will undergo the first BEST. At 0832 h, the participants receive a 2 min break (2nd intermission) and consume the final beverage of 250mL. At 0834 h, the participants undergo the second BEST. At 0844, the exercise bout will be completed. Participants will complete this protocol for each of the three experimental conditions.

Study Type

Interventional

Enrollment (Anticipated)

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 Contact

  • Name: Reed Zehr, BSc
  • Phone Number: 519-661-2111
  • Email: rzehr2@uwo.ca

Study Locations

    • Ontario
      • London, Ontario, Canada, N6A 3K7
        • Exercise Nutrition Laboratory (Western University)

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

16 years to 33 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Must be between 18-35 years old
  • Must be a Canadian Varsity Basketball Player

Exclusion Criteria:

  • Younger than 18 or older than 35
  • Not a Canadian Varsity Basketball Player

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: coconut water
participants will complete the simulated basketball game with coconut water supplementation
participants will consume coconut water and complete a simulated basketball game
Placebo Comparator: Placebo - water
participants will complete the simulated basketball game with water supplementation
participants will consume Placebo - water and complete a simulated basketball game
Experimental: Sports drink
participants will complete the simulated basketball game with sports drink supplementation
participants will consume a sports drink and complete a simulated basketball game

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Field Goal Percentage
Time Frame: 16 mins
shots made / shots attempted X 100
16 mins
Dribbles Performed
Time Frame: 5 minutes
number bounces
5 minutes
Total Sprint Decrement
Time Frame: 20 mins
100 x (total sprint time / ideal sprint time) - 100
20 mins
Distance run
Time Frame: 20 mins
meteres run
20 mins

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Rating of Perceived Exertion
Time Frame: 2 mins
Subjective rating from 6-20, 6 being easy and 20 being very, very hard
2 mins

Collaborators and Investigators

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

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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 (Anticipated)

April 15, 2018

Primary Completion (Anticipated)

October 30, 2018

Study Completion (Anticipated)

October 30, 2018

Study Registration Dates

First Submitted

April 6, 2018

First Submitted That Met QC Criteria

April 6, 2018

First Posted (Actual)

April 13, 2018

Study Record Updates

Last Update Posted (Actual)

April 13, 2018

Last Update Submitted That Met QC Criteria

April 6, 2018

Last Verified

April 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • 111166

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

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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