- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02702726
The Oil, Fats and Oleogel Study (OFO)
August 21, 2017 updated by: JeyaKumar Henry, Clinical Nutrition Research Centre, Singapore
The Oil, Fats and Oleogel (OFO) Study: Effects of Dietary Fats, Ingested in Two Physical Forms, on Acute Human Energy Balance, Appetitive and Glycemic Responses
The aim of this study is to compare the effects of dietary fats, ingested in two physical forms, on acute energy balance, appetitive, and glycemic responses of healthy normal (BMI 18-24.9
kgm-2) or overweight (BMI>25kgm-2) adults.
Study Overview
Status
Completed
Conditions
Detailed Description
This will be a randomised, crossover study.
Randomisation will be performed with an online randomisation software (www.randomizer.org).
Participants will be screened (1 screening visit) and attend five test visits conducted in a whole room calorimeter (WRC).
During each test visit, participants will arrive at the laboratory after an overnight fast, enter the WRC and rest for 15 minutes in a supine position,have their resting energy expenditure (REE) measured for 30 minutes and consume congee and juice alone(control), or with one of the 4 dietary fats: sunflower oil (SO) or gel (SG) and coconut oil (CO) or gel (CG) (total 5 test visits).
Post-meal energy expenditure, fat oxidation, glycemia and appetite (visual analog scales) will be measured continuously for 3 hours in WRC, followed by a meal challenge where participants will eat until sated.
Participants will return and repeat the protocol until all fat types and forms are completed.
Study Type
Interventional
Enrollment (Actual)
16
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
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-
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Singapore, Singapore, 117599
- Clinical Nutrition Research Centre
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-
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
21 years to 45 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Exclusion Criteria:
- People with major chronic disease such as heart disease, cancer, hypertension or diabetes mellitus
- People with known food allergies, due to potential traces of allergens found in the commercially available food product used in our study (Knorr's instant congee)
- People who are claustrophobic
- Individuals who are taking insulin or drugs known to affect glucose metabolism, appetite, and body fat distribution
- Have weight change of >5kg in the past 3 months
- People with a major medical or surgical event requiring hospitalization within the preceding three months
- People who are on a weight loss regime
- Individuals with the presence of disease or drugs which influence digestion and absorption of nutrients
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: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Congee and juice only
Control breakfast providing 50g carbohydrate
|
|
|
Active Comparator: Congee and juice with coconut gel
Control breakfast, plus 25g coconut oleogel (solid)
|
25g coconut oleogel
|
|
Active Comparator: Congee and juice with coconut oil
Control breakfast, plus 25g coconut oil (liquid)
|
25g coconut oil
|
|
Active Comparator: Congee and juice with sunflower gel
Control breakfast, plus 25g sunflower oleogel (solid)
|
25g sunflower oleogel
|
|
Active Comparator: Congee and juice with sunflower oil
Control breakfast, plus 25g sunflower oil (liquid)
|
25g sunflower oil
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
180-min postprandial energy expenditure (kJ/min over 180 minutes and total kJ/180-min session) measured by an indirect ventilated-hood calorimeter
Time Frame: 180 minutes
|
Gaseous exchanges obtained from the indirect calorimeter (volume of oxygen consumed and volume of carbon dioxide produced) will be used to calculate energy expenditure using the Weir equation: EE = 3.9 VO2 + 1.1 VCO2 [Weir, J. B. (1949).
"New methods for calculating metabolic rate with special reference to protein metabolism."
Journal of Physiology 109(1): 1-9]
|
180 minutes
|
|
180-min postprandial carbohydrate and fat oxidation (kJ/min over 180 minutes and total kJ and total grams during each session) measured by an indirect ventilated-hood calorimeter
Time Frame: 180 minutes
|
Gaseous exchanges obtained from the indirect calorimeter (volume of oxygen consumed and volume of carbon dioxide produced) will be used to calculate energy expenditure using the Frayn equations: carbohydrate oxidation = 4.55 VCO2 - 3.21 VO2; fat oxidation = 1.67 VO2 - 1.67 VCO2 [Frayn, K. N. (1983).
"Calculation of substrate oxidation rates in vivo from gaseous exchange."
Journal of Applied Physiology 55(2): 628-634]
|
180 minutes
|
|
Post-test-meal capillary blood glucose (mmol/L) at 0, 15, 30, 45, 60, 90, 120, 150, 180 minutes
Time Frame: 180 minutes
|
Capillary blood glucose will be assessed at 0, 15, 30, 45, 60, 90, 120, 150, 180 minutes using a Hemocue system (HemoCue Glucose 201 RT Systems, Helsingborg, Sweden)
|
180 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Post-test-meal subjective appetite measurements at 0, 15, 30, 45, 60, 90, 120, 150, 180 minutes
Time Frame: 180 minutes
|
Appetite ratings will be collected at 0, 15, 30, 45, 60, 90, 120, 150, 180 minutes after test meal consumption using a previously validated visual analog scales [Flint, A., A. Raben, J. E. Blundell and A. Astrup (2000).
"Reproducibility, power and validity of visual analogue scales in assessment of appetite sensations in single test meal studies."
International Journal of Obesity 24(1): 38-48]
|
180 minutes
|
|
Free-living food intake after completion of test session
Time Frame: 180 minutes
|
Participants will be asked to keep a food record that document the types and amount of food and beverage they consume after they leave the research centre, until they go to bed on the same day.
Data will be analysed using nutrient analysis software.
|
180 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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)
January 12, 2016
Primary Completion (Actual)
May 23, 2017
Study Completion (Actual)
May 23, 2017
Study Registration Dates
First Submitted
February 29, 2016
First Submitted That Met QC Criteria
March 3, 2016
First Posted (Estimate)
March 9, 2016
Study Record Updates
Last Update Posted (Actual)
August 23, 2017
Last Update Submitted That Met QC Criteria
August 21, 2017
Last Verified
August 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- 2015/01093
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
IPD Plan Description
Not applicable for this study
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.