Whey Protein Supplementation in High School Athletes
- Conditions
- Body Weight ChangesAthletic PerformanceRecoverySleep
- Interventions
- Dietary Supplement: Carbohydrate Placebo ControlDietary Supplement: Whey Protein Supplement
- Registration Number
- NCT05589129
- Lead Sponsor
- University of Utah
- Brief Summary
The overall aim of this project is to compare protein supplementation on performance, recovery, and body composition changes in adolescent soccer players between the whey protein and the control group in response to the 10-12-week intervention.
- Detailed Description
Informed Consent, Parental Permission and Assent: These will be obtained over Zoom, prior to participation in any study procedures.
Randomization: Randomization will occur following baseline testing. Participants will be randomized via random number generator stratified by sex, into either the whey protein supplement group or the placebo (isocaloric) control group.
Baseline and Post-Intervention testing will occur over a single day for each participant.
Baseline:
All athletes will report to testing facilities for a single blood draw to measure inflammatory biomarkers and a body composition assessment (via BodPod) to measure fat mass and fat free mass. Participants will then be escorted to a track where they will run a 30-yard dash to assess their speed and a 1.5-mile run to assess their estimated maximal rate of oxygen consumption (VO2max). Participants will then be transferred back to the testing facility where they will undergo assessment of lower body muscle fatigue (via HumacNorm).
Questionnaires: Athletes will complete the Munich Chronotype Questionnaire and the Pittsburg Sleep Quality Index (PSQI). Participants will also complete 3-day, 24-hour dietary recalls (via ASA-24).
Sleep measures: Fitbit (Inspire 2) will be used measure sleep efficiency, duration, and staging. Fitabase will be utilized to receive Fitbit data. Participants will be instructed to wear their Fitbit for 1-week.
Intervention:
In-season soccer practices and competition will occur 6-days per week across a 10-12 week period, depending on how far teams advance in postseason play. During the 10-12-weeks, participants will consume their assigned supplement or placebo twice per day, every day, immediately after practice or competition (or midday on rest days), and \~1 hour before bedtime.
Sleep measures: Sleep measures will be evaluated as described above. Sleep measures will be collected at weeks 2, 4, 6, 8, and 10.
Questionnaires: Participants will complete 3-days of 24-hour dietary recalls (via ASA-24) at weeks 5 and 10. Pittsburg Sleep Quality Index (PSQI), a delayed-onset muscle soreness questionnaire and a GI symptom Questionnaire will be completed at weeks 2, 4, 6, 8 and 10.
Urine Samples: We will randomly assign participants to provide urine samples at weeks 4 and 7 as a sham measure of compliance to supplementation protocol.
Post-testing will be the same as pre-testing and will commence after the 10-12-week competitive season. All measures described above in baseline testing will be repeated.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 31
- 13-18 years old; male and female High school soccer players
- non-adolescents; untreated or underlying metabolic or cardiovascular diseases; allergies to dairy, or any allergies ingredients in the study provided granola bar or bagels, such as soy, wheat, tree nuts, peanuts, milk, and sesame.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Carbohydrate Control Carbohydrate Placebo Control Carbohydrate control will come in powder form and will consist of 20g of carbohydrate and 21.6g of product. We will use Nesquick Chocolate Powder mix. Whey Protein Supplement Whey Protein Supplement Whey protein will come in powder form and will consist of 20g of protein, and 25.3g of product. We will use Optimum Nutrition Double Chocolate Whey Protein Isolate.
- Primary Outcome Measures
Name Time Method Changes in Fat Mass Measured at baseline and post-intervention (10-12-weeks) Measured via BodPod
Changes in Fat Free Mass Measured at baseline and post-intervention (10-12-weeks) Measured via BodPod
- Secondary Outcome Measures
Name Time Method Sleep Efficiency Measured at baseline, 2-, 4-, 6-, 8-weeks and post-intervention (10-12-weeks) Measured via Fitbit devices. Sleep efficiency is measured based on how long and individual is asleep over the time spent in bed during the night.
Changes in Speed Measured at baseline and post-intervention (10-12-weeks) 30 yard sprint
Sleep Staging Measured at baseline, 2-, 4-, 6-, 8-weeks and post-intervention (10-12-weeks) Measured via Fitbit devices. Sleep stages are different periods of sleep where muscle tone and heart rate vary.
Estimated Cardiorespiratory Fitness (V02max) Measured at baseline and post-intervention (10-12-weeks) Measured via 1.5-mile run time
Changes in Muscular Fatigue Measured at baseline and post-intervention (10-12-weeks) Measured via leg extension machine (HumacNorm) using isometric muscle contraction in the quadriceps muscle.
Sleep Duration Measured at baseline, 2-, 4-, 6-, 8-weeks and post-intervention (10-12-weeks) Measured via Fitbit devices. Sleep duration is measured based on how long the individual is asleep.
Trial Locations
- Locations (1)
Grace Zimmerman
đŸ‡ºđŸ‡¸Salt Lake City, Utah, United States