Original Query: ALL
Previous Study | Return to List | Next Study

Overnight Post-Exercise Recovery After Protein Ingestion Prior to Sleep

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. Identifier: NCT00991523
Recruitment Status : Completed
First Posted : October 8, 2009
Last Update Posted : April 20, 2011
Information provided by:
Maastricht University Medical Center

Brief Summary:
The purpose of this study is to examine the effects of post-exercise protein ingestion prior to sleep on overnight protein kinetics and muscle recovery.

Condition or disease Intervention/treatment
Exercise Resistance Training Dietary Supplement: protein Dietary Supplement: placebo

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 24 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Basic Science
Official Title: Protein Ingestion Prior to Sleep as a Dietary Strategy to Improve Post-exercise, Overnight Recovery.
Study Start Date : October 2009
Primary Completion Date : August 2010
Study Completion Date : December 2010

Resource links provided by the National Library of Medicine

U.S. FDA Resources

Arm Intervention/treatment
Experimental: sweetened beverage Dietary Supplement: protein
Placebo Comparator: placebo control
Dietary Supplement: placebo
placebo control

Primary Outcome Measures :
  1. muscle protein synthesis [ Time Frame: 10 hours ]

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Ages Eligible for Study:   20 Years to 30 Years   (Adult)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Male
  • Age between 20 and 30 years
  • Healthy, recreationally active
  • BMI <25 kg/m2

Exclusion Criteria:

  • Use of medication

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00991523

Maastricht MUMC
Maastricht, LI, Netherlands, 6202
Maastricht, Netherlands
Sponsors and Collaborators
Maastricht University Medical Center
Principal Investigator: Luc van Loon, PhD Maastricht University Medical Center

Publications automatically indexed to this study by Identifier (NCT Number):
Responsible Party: Luc van Loon, University Hospital Maastricht Identifier: NCT00991523     History of Changes
Other Study ID Numbers: MEC 09-3-054
First Posted: October 8, 2009    Key Record Dates
Last Update Posted: April 20, 2011
Last Verified: April 2011

Keywords provided by Maastricht University Medical Center: