- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02764177
Resistance Exercise, Recovery Drinks and Appetite
May 5, 2016 updated by: Lewis James, Loughborough University
Effect of Recovery Drink Composition Consumed After Resistance Exercise on Subsequent Appetite and Energy Intake
Whilst the effects of manipulating the macronutrient content of foods on appetite and energy intake has been relatively well studied at rest, little is known about these responses in a post-exercise context.
The effect of post-exercise nutrition on recovery from or adaptation to exercise has been well studied.
However, many exercisers do so for weight management and thus any post-exercise nutrition might impact on energy balance and might need to be carefully considered.
This study will examine the impact of manipulating the composition of a recovery drink consumed after resistance exercise on subsequent appetite and energy intake.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Subjects perform a bout of lower body resistance exercise lasting ~50 min and immediately post-exercise they consume one of two recovery drinks over a 5 min period.
Over the next 60 min subjective appetite responses will be measured and then 60 min after drink ingestion, subjects will consume an ad-libitum meal.
Study Type
Interventional
Enrollment (Actual)
15
Phase
- Not Applicable
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 60 years (Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Generally fit and healthy
- Use resistance exercise as part of weekly training
- Weight stable in previous 6 months
Exclusion Criteria:
- Smoker
- History of gastric, digestive, cardiovascular or renal disease
- Lactose, dairy, gluten intolerances or allergies
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: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Protein
In this arm the subjects were provided with a PROTEIN drink to consume after exercise.
This protein drink contained whey protein isolate that provided 0.3 g/ kg body mass of protein.
|
The protein drink was administered during this trial
|
Experimental: Carbohydrate
In this arm the subjects were provided with a CARBOHYDRATE drink to consume after exercise.
This carbohydrate drink was energy matched to the protein drink in the other arm of the experiment.
|
The carbohydrate drink was administered in this trial
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Ad-libitum energy intake
Time Frame: 65 min post-exercise
|
Assessed via a homogenous pasta meal
|
65 min post-exercise
|
Subjective appetite (hunger)
Time Frame: 150 min
|
Assessed via 100 mm visual analogue scales
|
150 min
|
Subjective appetite (fullness)
Time Frame: 150 min
|
Assessed via 100 mm visual analogue scales
|
150 min
|
Subjective appetite (desire to eat)
Time Frame: 150 min
|
Assessed via 100 mm visual analogue scales
|
150 min
|
Subjective appetite (prospective food consumption)
Time Frame: 150 min
|
Assessed via 100 mm visual analogue scales
|
150 min
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pleasantness of study drinks
Time Frame: Immediately after drinking
|
Assessed via 100 mm visual analogue scales
|
Immediately after drinking
|
Aftertaste of study drinks
Time Frame: Immediately after drinking
|
Assessed via 100 mm visual analogue scales
|
Immediately after drinking
|
Saltiness of study drinks
Time Frame: Immediately after drinking
|
Assessed via 100 mm visual analogue scales
|
Immediately after drinking
|
Bitterness of study drinks
Time Frame: Immediately after drinking
|
Assessed via 100 mm visual analogue scales
|
Immediately after drinking
|
Sweetness of study drinks
Time Frame: Immediately after drinking
|
Assessed via 100 mm visual analogue scales
|
Immediately after drinking
|
Creaminess of study drinks
Time Frame: Immediately after drinking
|
Assessed via 100 mm visual analogue scales
|
Immediately after drinking
|
Thickness of study drinks
Time Frame: Immediately after drinking
|
Assessed via 100 mm visual analogue scales
|
Immediately after drinking
|
Stickiness of study drinks
Time Frame: Immediately after drinking
|
Assessed via 100 mm visual analogue scales
|
Immediately after drinking
|
Fruitiness of study drinks
Time Frame: Immediately after drinking
|
Assessed via 100 mm visual analogue scales
|
Immediately after drinking
|
Refreshment of study drinks
Time Frame: Immediately after drinking
|
Assessed via 100 mm visual analogue scales
|
Immediately after drinking
|
Eating rate
Time Frame: 65 min post-exercise
|
mean eating rate determined at ad-libitum meal
|
65 min post-exercise
|
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
October 1, 2014
Primary Completion (Actual)
December 1, 2015
Study Completion (Actual)
December 1, 2015
Study Registration Dates
First Submitted
May 4, 2016
First Submitted That Met QC Criteria
May 4, 2016
First Posted (Estimate)
May 6, 2016
Study Record Updates
Last Update Posted (Estimate)
May 9, 2016
Last Update Submitted That Met QC Criteria
May 5, 2016
Last Verified
May 1, 2016
More Information
Terms related to this study
Other Study ID Numbers
- R15-P106
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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