- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02667340
Superstarch and Physical/Cognitive Performance Following a Simulated Soccer Game
Effects of Starch Produced From Heat-treated Corn (Superstarch) Supplementation on Skills, Cognitive Function and Physical Performance During/Following a Simulated Soccer Game
To assess the efficacy of a hydrothermally modified starch supplement (Superstarch made byGeneration UCAN) vs isoenergetic placebo (glucose) on exercise performance, execution of specific soccer skills, and on cognitive function during and following a simulated soccer game.
Secondary: To compare fat oxidation and carbohydrate oxidation (based on RER data) during the game with Generation UCAN vs isoenergetic placebo (glucose).
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- healthy male and female elite soccer players who are involved in regular soccer training
- aged 15-35 years
Exclusion Criteria:
- Smoker
- taking part in other research
- have a neurological or psychiatric condition that may cause cognitive dysfunction
- for women, if they are pregnant or become pregnant during the study
- Injury limiting exercise ability
Study Plan
How is the study designed?
Design Details
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Superstarch
Supplementation with Superstarch before a simulated soccer game
|
0.7 g Superstarch or placebo per kg body mass in two ingestions (before game & at halftime)
Other Names:
|
Placebo Comparator: Placebo
Supplementation with placebo before simulated soccer game.
|
0.7 g glucose per kg body mass in two ingestions (before game & at halftime)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
change in exercise performance
Time Frame: baseline; 60 minutes later (following soccer game)
|
sprint run test (seconds); soccer skills (seconds), cognitive skills (seconds)
|
baseline; 60 minutes later (following soccer game)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
change in blood glucose concentration
Time Frame: baseline; 60 minutes later
|
mmols/l
|
baseline; 60 minutes later
|
change in blood lactate concentration
Time Frame: baseline, 60 minutes later
|
mmols/l
|
baseline, 60 minutes later
|
Collaborators and Investigators
Investigators
- Principal Investigator: Pete W Lemon, PhD, Western University
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 10009797
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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