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Clinical Trials/NCT03947801
NCT03947801CompletedNot Applicable

Dairy Consumption During a High-intensity, High-volume Training Week in Young Athletes

Brock University2 sites in 1 country30 target enrollmentStarted: July 1, 2019Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
30
Locations
2
Primary Endpoint
Height (cm)

Study Overview

Brief Summary

Our proposed study is a 5-d double-blind randomised cross-over trial, seeking to simulate a training identification camp in competitive adolescent soccer players

The purpose of the proposed study is to investigate whether increased protein consumption by Greek yogurt, compared to an isoenergetic carbohydrate (CHO) control supplement, consumed immediately following exercise training, prior to sleep and between breakfast and lunch, for a week during an intense training period (high volume, high intensity) will:

  • Attenuate the pro-inflammatory response (cytokines, acute phase proteins)
  • Reduced the severity of muscle damage and impairment (creatine kinase)
  • Maintain performance

Secondary outcome measures:

  • Increase bone turnover (in favour of formation)

Detailed Description

The proposed study is a randomized, double-blinded, cross-over trial. The protocol will consist of an information session, two identical training camps consisting of 5 consecutive days of intensified soccer training, differing only by nutritional intervention, and identical pre-and post-training session testing. Each testing block will be separated by 28-d to allow for an adequate wash-out and recovery period, during which participants would resume their regular soccer activities

Study Procedures:

All tests and measurements will be performed within eight-weeks. Specifically, participants will attend 1 information session, two identical pre- and post- training/testing sessions and two identical soccer specific training camps.

Information session:

One week prior to the initial soccer specific training camp, participants will be informed of all tests and procedures that will take place and be familiarized with all testing protocols.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Other
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
11 Years to 16 Years (Child)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Participant are female within the desired age ranges (11-16y)
  • Participants are competitive soccer players
  • Previous participation in high-performance training environment (periodization)

Exclusion Criteria

  • Participant is not female or falls outside of the desired age ranges (11-16y)
  • Chronic/frequent use of medications that could affect inflammatory function - NSAIDS or Corticosteroids.
  • Musculoskeletal injury - resulting in the inability to train and/or perform the baseline/post testing.

Outcomes

Primary Outcomes

Height (cm)

Time Frame: 8 weeks

Anthropometric measures

Plasma concentrations of CRP (pg/ml)

Time Frame: 8 weeks

Plasma concentrations of pro-and-anti-inflammatory cytokines

Body fat (%)

Time Frame: 8 weeks

Body composition

Serum concentrations of OPG (pg/ml)

Time Frame: 8 weeks

Bone formation marker

Serum concentrations of TRAP (ng/ml)

Time Frame: 8 weeks

Bone resorption marker

Serum concentrations of CTX (ng/ml)

Time Frame: 8 weeks

Bone resorption marker

Body mass (kg)

Time Frame: 8 weeks

Anthropometric measures

Serum concentrations of BAP (ng/ml)

Time Frame: 8 weeks

Bone formation marker

Serum concentrations of PINP (ng/ml)

Time Frame: 8 weeks

Bone formation marker

Serum concentrations of RANKL (pg/ml)

Time Frame: 8 weeks

Bone resorption marker

Plasma concentrations of IL-6 (pg/ml)

Time Frame: 8 weeks

Plasma concentrations of pro-and-anti-inflammatory cytokines

Plasma concentration of creatine kinase (U/L)

Time Frame: 8 weeks

Muscle damage

Seated height (cm)

Time Frame: 8 weeks

Used to calculate maturity offset in years from peak height velocity

Rate of perceived exertion

Time Frame: 8 weeks

1-10 scale of perceived exertion

Plasma concentrations of TNF-alpha (pg/ml)

Time Frame: 8 weeks

Plasma concentrations of pro-and-anti-inflammatory cytokines

Plasma concentrations of irisin (ng/ml)

Time Frame: 8 weeks

Plasma concentrations of pro-and-anti-inflammatory cytokines

Plasma concentrations of IL-10 (pg/ml)

Time Frame: 8 weeks

Plasma concentrations of pro-and-anti-inflammatory cytokines

Secondary Outcomes

  • Plasma concentration of ROS(8 weeks)
  • Serum concentration of IGF-1 (pg/ml)(8 weeks)
  • Plasma concentration of TBARS(8 weeks)
  • Saliva concentrations of cortisol (ug/dl)(8 weeks)
  • Saliva concentrations of testosterone (pg/ml)(8 weeks)
  • Oxidative stress(8 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

PKlentrou

Professor and Associate Dean

Brock University

Study Sites (2)

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