- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03147833
Protein Before Night Sleep to Improve Recovery and Performance in Runners
June 7, 2018 updated by: Mette Hansen, University of Aarhus
Ingestion of Protein Before Each Night Sleep to Improve Recovery and Performance in Runners
32 runners will be randomized into two groups.
The duration of the intervention is one week including a strenuous endurance training program.
Group 1 receive a protein beverage before each night sleep and Group 2 receive an isocaloric carbohydrate beverage.
Performance test before and after the intervention and blood sampling before and during the intervention to check for markers for muscle damage.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
32
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Aarhus, Denmark, 8000
- Aarhus University, Department for Public Health, Section for Sport Science
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 50 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Description
Inclusion Criteria: VO2max >55 ml O2/kg/min -
Exclusion Criteria:women, smokers
-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Sport beverages Protein
Intervention group ingesting PROTEIN
|
Beverage ingested before each night sleep during the intervention
|
Active Comparator: Sports beverage Carbohydrate
Placebo group ingesting carbohydrate
|
Beverage ingested before each night sleep during the intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Performance
Time Frame: 8 days
|
5 km time trial
|
8 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Muscle damage
Time Frame: 8 days
|
creatine kinase
|
8 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 1, 2017
Primary Completion (Actual)
October 9, 2017
Study Completion (Actual)
October 9, 2017
Study Registration Dates
First Submitted
May 8, 2017
First Submitted That Met QC Criteria
May 8, 2017
First Posted (Actual)
May 10, 2017
Study Record Updates
Last Update Posted (Actual)
June 11, 2018
Last Update Submitted That Met QC Criteria
June 7, 2018
Last Verified
June 1, 2018
More Information
Terms related to this study
Other Study ID Numbers
- 1107229216
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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