- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03917810
Acute Responses to Manipulating Dietary Carbohydrate Content on Free-living Physical Activity Energy Expenditure
Dietary sugar and carbohydrate intakes will be manipulated for 3 days in a randomised crossover design. All food will be provided. Free-living physical activity energy expenditure will be measured using combined heart rate and accelerometry. Metabolic and appetite/mood responses to 3 days on each diet will be measured.
Each participant will undergo 3 days of each diet:
- Moderate sugar - reflecting the composition of a typical European diet
- Low sugar - similar macronutrient composition of a typical European diet but with <5% energy intake from free sugars (as per government guidelines)
- Low carbohydrate - low carbohydrate diet with <5% energy intake from sugar and <8% energy intake from carbohydrate, replacing carbohydrate energy with fat
Study Overview
Detailed Description
Guidelines calling for dietary free sugars to be reduced have been formulated from evidence that diets high in sugar are associated with high energy intake. In theory, by reducing the intake of sugars, calorie surplus will be reduced and energy balance will be maintained. However, when referring to interventions/behaviours that influence energy balance, both sides of the energy balance equation need to be considered. Alterations in nutrients may influence aspects of energy expenditure, not solely energy intake, and this may have implications for the efficacy of guidelines seeking to influence energy intake.
It is important to consider energy expenditure in the context of health. The most variable component of energy expenditure between individuals is physical activity energy expenditure (PAEE), which varies from ~600-2100 kcal per day in men of a similar demographic. Current guidelines do not regard the effect that changing dietary sugar might have on PAEE and therefore total energy expenditure.
Furthermore, there is increasing interest in restricting overall carbohydrate intake to treat metabolic disease or achieve ketogenesis. Very little is known about nutrition-physical activity interactions with this type of intervention.
This study will prescribe 3 diets to healthy males for 3 days in a randomised crossover design, where each participant will consume each of the diets. All food will be prepared and provided by the study team. The diets are as follows:
- Moderate sugar - reflecting the composition of a typical European diet
- Low sugar - similar macronutrient composition of a typical European diet but with <5% energy intake from free sugars (as per government guidelines)
- Low carbohydrate - low carbohydrate diet with <5% energy intake from sugar and <8% energy intake from carbohydrate, replacing carbohydrate energy with fat
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Somerset
-
Bath, Somerset, United Kingdom, BA2 7AY
- University of Bath
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Body mass index 18.5-29.9 kg∙m-2
- Age 18-65 years
- Male
- Able and willing to provide informed consent and safely comply with study procedures
- No anticipated changes in physical activity during the study (e.g. holidays)
Exclusion Criteria:
- Any reported condition or behaviour deemed either to pose undue personal risk to the participant or introduce bias
- Any diagnosed metabolic disease (e.g. type 1 or type 2 diabetes)•Any reported use of substances which may pose undue personal risk to the participants or introduce bias into the experiment
- Lifestyle not conforming to standard sleep-wake cycle (e.g. shift worker)
- Any reported recent (<6 months) change in body mass (±3%)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: MODSUG
Diet consisting of 50% carbohydrate (20% sugar), 15% protein, 35% fat
|
Macronutrient composition (specifically type and/or amount of carbohydrate) is manipulated
|
|
Experimental: LOWSUG
Diet consisting of 50% carbohydrate (<5% sugar), 15% protein, 35% fat
|
Macronutrient composition (specifically type and/or amount of carbohydrate) is manipulated
|
|
Experimental: LOWCHO
Diet consisting of <8% carbohydrate (<5% sugar), 15% protein, >77% fat
|
Macronutrient composition (specifically type and/or amount of carbohydrate) is manipulated
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Physical activity energy expenditure (kj/day or kcal/day)
Time Frame: 3 days
|
Physical activity energy expenditure measured using individually-calibrated combined heart rate and accelerometry (kj/day or kcal/day)
|
3 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Time spent in different physical activity intensities (MET categories) (minutes)
Time Frame: 3 days
|
Time spent in different physical activity intensities (MET categories) (minutes) using individually-calibrated combined heart rate and accelerometry
|
3 days
|
|
Energy expended in different physical activity intensities (MET categories) (kJ/day or kcal/day)
Time Frame: 3 days
|
Energy expended in different physical activity intensities (MET categories) (kJ/day or kcal/day) using individually-calibrated combined heart rate and accelerometry
|
3 days
|
|
Energy expended in the postprandial period (kJ or kcal)
Time Frame: 3 days
|
Energy expended in the postprandial period (kJ or kcal) measured using individually-calibrated combined heart rate and accelerometry
|
3 days
|
|
Fasting blood glucose concentrations
Time Frame: 3 days
|
Measures of blood glucose concentrations pre- and post-intervention.
|
3 days
|
|
Fasting blood insulin concentrations
Time Frame: 3 days
|
Measures of blood insulin concentrations pre- and post-intervention.
|
3 days
|
|
Fasting blood triglyceride concentrations
Time Frame: 3 days
|
Measures of blood triglyceride concentrations pre- and post-intervention.
|
3 days
|
|
Fasting blood non-esterified fatty acid concentrations
Time Frame: 3 days
|
Measures of blood non-esterified fatty acid concentrations pre- and post-intervention.
|
3 days
|
|
Fasting blood lactate concentrations
Time Frame: 3 days
|
Measures of blood lactate concentrations pre- and post-intervention.
|
3 days
|
|
Fasting blood beta-hydroxybutyrate concentrations
Time Frame: 3 days
|
Measures of blood beta-hydroxybutyrate concentrations pre- and post-intervention.
|
3 days
|
|
Fasting blood leptin concentrations
Time Frame: 3 days
|
Measures of blood leptin concentrations pre- and post-intervention.
|
3 days
|
|
Fasting blood fibroblast growth factor-21 concentrations
Time Frame: 3 days
|
Measures of blood fibroblast growth factor-21 concentrations pre- and post-intervention.
|
3 days
|
|
Fasting blood total cholesterol concentrations
Time Frame: 3 days
|
Measures of blood total cholesterol concentrations pre- and post-intervention.
|
3 days
|
|
Fasting blood high density lipoprotein concentrations
Time Frame: 3 days
|
Measures of blood high density lipoprotein concentrations pre- and post-intervention.
|
3 days
|
|
Fasting blood low density lipoprotein concentrations
Time Frame: 3 days
|
Measures of blood low density lipoprotein concentrations pre- and post-intervention.
|
3 days
|
|
Food preference ratings
Time Frame: 3 days
|
Food preference ratings determined by computer task measured pre- and post-intervention
|
3 days
|
|
Subjective appetite and mood ratings
Time Frame: 3 days
|
Measured by 0-100 mm visual analogue scales measured pre- and post-intervention
|
3 days
|
|
Blood pressure
Time Frame: 3 days
|
Blood pressure using an automated sphygmomanometer pre- and post-intervention
|
3 days
|
Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Betts JA, Richardson JD, Chowdhury EA, Holman GD, Tsintzas K, Thompson D. The causal role of breakfast in energy balance and health: a randomized controlled trial in lean adults. Am J Clin Nutr. 2014 Aug;100(2):539-47. doi: 10.3945/ajcn.114.083402. Epub 2014 Jun 4.
- Smith HA, Gonzalez JT, Thompson D, Betts JA. Dietary carbohydrates, components of energy balance, and associated health outcomes. Nutr Rev. 2017 Oct 1;75(10):783-797. doi: 10.1093/nutrit/nux045.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- EP 17/18 219
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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