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Trial record 17 of 496 for:    Supplement | maltodextrin

Whole Milk Versus Whey Protein Supplement and Resistance Exercise

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01580189
Recruitment Status : Completed
First Posted : April 18, 2012
Last Update Posted : December 8, 2015
Sponsor:
Information provided by (Responsible Party):
University of Manitoba

Tracking Information
First Submitted Date  ICMJE April 16, 2012
First Posted Date  ICMJE April 18, 2012
Last Update Posted Date December 8, 2015
Study Start Date  ICMJE October 2011
Actual Primary Completion Date October 2012   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: April 17, 2012)
  • Body composition [ Time Frame: 9 weeks ]
    DEXA for assessment of fat and lean tissue
  • Strength [ Time Frame: 9 weeks ]
    1RM tests to assess changes in strength on various sport resistant exercise equipment
Original Primary Outcome Measures  ICMJE Same as current
Change History Complete list of historical versions of study NCT01580189 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures  ICMJE
 (submitted: April 17, 2012)
Blood amino acid [ Time Frame: 9 weeks ]
Assessment of plasma amino acid profile at baseline, mid and end of the study.
Original Secondary Outcome Measures  ICMJE Same as current
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE Whole Milk Versus Whey Protein Supplement and Resistance Exercise
Official Title  ICMJE Effects of Whole Milk Versus Whey Protein Supplementation With Resistance Exercise on Body Composition, Muscle Hypertrophy and Strength Changes in Healthy Individuals
Brief Summary The purpose of the study is to examine the effects of consuming protein supplement (whey) compared to whole milk immediately after bouts of resistance training on muscular strength and body composition.
Detailed Description Not Provided
Study Type  ICMJE Interventional
Study Phase  ICMJE Not Applicable
Study Design  ICMJE Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Basic Science
Condition  ICMJE Muscle Development
Intervention  ICMJE
  • Dietary Supplement: Whey protein
    18g protein, immediately after training, 9 weeks
    Other Name: protein supplement
  • Dietary Supplement: Chocolate milk
    500ml chocolate milk, immediately after training, 9 weeks
    Other Name: Milk
  • Dietary Supplement: Sugar
    55-65g maltodextrin solution, immediately after training, 9 weeks
    Other Name: Maltodextrin
Study Arms  ICMJE
  • Active Comparator: Milk
    Chocolate milk compared to protein supplement
    Intervention: Dietary Supplement: Whey protein
  • Active Comparator: Whey protein
    Whey protein compared to milk
    Intervention: Dietary Supplement: Chocolate milk
  • Placebo Comparator: Sugar
    Maltodextrin compared to treatments
    Intervention: Dietary Supplement: Sugar
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Completed
Actual Enrollment  ICMJE
 (submitted: August 12, 2013)
32
Original Estimated Enrollment  ICMJE
 (submitted: April 17, 2012)
24
Actual Study Completion Date  ICMJE December 2013
Actual Primary Completion Date October 2012   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion Criteria:

  • healthy
  • currently working out at least 3 times per week

Exclusion Criteria:

  • taken any ergogenic aid/sport supplements in the last 2 months
Sex/Gender  ICMJE
Sexes Eligible for Study: All
Ages  ICMJE 18 Years to 35 Years   (Adult)
Accepts Healthy Volunteers  ICMJE Yes
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE Canada
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT01580189
Other Study ID Numbers  ICMJE B2011:068
Has Data Monitoring Committee Yes
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement  ICMJE Not Provided
Responsible Party University of Manitoba
Study Sponsor  ICMJE University of Manitoba
Collaborators  ICMJE Not Provided
Investigators  ICMJE
Principal Investigator: Semone B Myrie, PhD University of Manitoba
PRS Account University of Manitoba
Verification Date December 2015

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP