- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05658133
Understanding Sports Nutrition Knowledge of High School Athletes and Influencers
The objective of this testing is to gain a better understanding of sports nutrition knowledge in high school athletes and their influencers (coaches, strength and conditioning coaches, athletic therapists, dieticians). Since the sports nutrition knowledge of the high school athletes will be limited, nutrition behaviors will be assessed to infer knowledge of sports nutrition.
The secondary objective is to determine the primary sources of nutrition knowledge in these populations.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Florida
-
Bradenton, Florida, United States, 34210
- Remote survey, no facility visits. Survey managed by PepsiCo at IMG Academy
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria for Athletes
- Participants are male or female between 14-19 years of age, inclusive.
- Participants must be participating on a high school varsity team, or Amateur Athletic Union, National, or State travel team.
- Participants must be attending high school in the United States.
- Participant understands what is required to complete the study and signs forms providing informed consent to complete the questionnaire
- Participant or legal guardian is able and willing to sign the Informed Consent Form.
Inclusion Criteria for Influencers
- Participants must be currently coaching, or a practitioner for a high school varsity team, or an Amateur Athletic Union, National, or State, travel team of high school students aged (14-19 years).
- Participants must work with/at a high school in the United States.
- Participant understands what is required to complete the study and signs forms providing informed consent to complete the questionnaire
Exclusion Criteria for Athletes
- Participant has a condition the Investigator believes would interfere with his or her ability to provide informed consent, which might put the individual at undue risk.
- Participant is pregnant.
Exclusion Criteria for Influencers
1. Participant has a condition the Investigator believes would interfere with his or her ability to provide informed consent, which might put the individual at undue risk.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Survey for student athletes
15 to 20 minute online questionnaire completed using Qualtrics
|
Questionnaire
|
|
Other: Survey for influencers of student athletes
15 to 20 minute online questionnaire completed using Qualtrics
|
Questionnaire
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Better understand the level of sports nutrition knowledge of high school athletes
Time Frame: To complete a one-time 15 to 20 minute online questionnaire they may access at any time using a cell phone, computer, or tablet.
|
Measured by determining the number of respondents that score greater than 75 percent on the sports nutrition knowledge questionnaire.
A higher score is better than a lower score.
|
To complete a one-time 15 to 20 minute online questionnaire they may access at any time using a cell phone, computer, or tablet.
|
|
Better understand the level of sports nutrition knowledge of influencers of high school athletes
Time Frame: To complete a one-time 15 to 20 minute online questionnaire they may access at any time using a cell phone, computer, or tablet.
|
Measured by determining the number of respondents that score greater than 75 percent on the sports nutrition knowledge questionnaire.
A higher score is better than a lower score.
|
To complete a one-time 15 to 20 minute online questionnaire they may access at any time using a cell phone, computer, or tablet.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Determine the primary sources of information for sports nutrition knowledge from high school athletes
Time Frame: To complete a one-time 15 to 20 minute online questionnaire they may access at any time using a cell phone, computer, or tablet.
|
Measured by the sources if information selected in the survey.
Credible sources of information would be better.
|
To complete a one-time 15 to 20 minute online questionnaire they may access at any time using a cell phone, computer, or tablet.
|
|
Determine the primary sources of information for sports nutrition knowledge from influencers of high school athletes
Time Frame: To complete a one-time 15 to 20 minute online questionnaire they may access at any time using a cell phone, computer, or tablet.
|
Measured by the sources if information selected in the survey.
Credible sources of information would be better.
|
To complete a one-time 15 to 20 minute online questionnaire they may access at any time using a cell phone, computer, or tablet.
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sara Oikawa, PhD, PepsiCo, Inc. Sports Science
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Keywords
Other Study ID Numbers
- PEP-2109
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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