- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03497858
The Effect of Coconut Water on Varsity Basketball Performance
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
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
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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