Comparison of the Effect of MCFA and LCFA on Postprandial Appetite and Lipemia
Lipemia
About this trial
This is an interventional treatment trial for Lipemia focused on measuring Postprandial lipemia
Eligibility Criteria
Inclusion Criteria:
- Age between 18-50 years
- Males and females
- Apparently healthy
- Fasting triglyceride (TG) < 2.5 mmol/L or 222 mg/dl at the time of screening.
- Body mass index (BMI) in normal range (18.5-24.9).
- Stable weight for at least 3 months
Exclusion Criteria:
- Consumption of lipid-lowering drugs or any medication that might affect appetite.
- Consumption of any supplement that may affect lipid metabolism or appetite on a regular basis for the past month.
- Regular consumption of two or more fish meals a week over the previous month.
- A history of diabetes, gastrointestinal , liver disease, congestive heart failure, stroke, myocardial infarction, coronary artery bypass graft or established atherosclerotic disease.
- Current smokers
- Pregnant , breastfeeding, postmenopausal or suffer from polycystic ovary syndrome (PCOS)
- Athlete
- Being on a diet or lifestyle changes for the past month.
Sites / Locations
- The University of Jordan
- The University of Jordan
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Coconut oil
Palm oil
The coconut oil will be given to each participant in the amount of 40 g, which will be incorporated into biscuits. Each participant will have ten minutes to consume biscuits with 250 ml of water. No other food will be consumed during the study period (6 hours). After that, participants will be allowed an ad libitum intake of standard meals. Each meal will be weighed before and after it is consumed, with the amount of food ingested being calculated. Then the participants will take the other treatment after a 1-week washout interval.
The palm oil will be given to each participant in the amount of 40 g, which will be incorporated into biscuits. Each participant will have ten minutes to consume biscuits with 250 ml of water. No other food will be consumed during the study period (6 hours). After that, participants will be allowed an ad libitum intake of standard meals. Each meal will be weighed before and after it is consumed, with the amount of food ingested being calculated. Then the participants will take the other treatment after a 1-week washout interval.