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Appetite clinical trials

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NCT ID: NCT01222845 Completed - Appetite Clinical Trials

Glycaemic, Insulinaemic and Appetite Responses to Two Different Types of Porridge

Start date: October 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the postprandial glycaemic, insulinaemic and appetite responses to porridge made with oats processed differently.

NCT ID: NCT01199770 Completed - Healthy Clinical Trials

Pasta Formulations, Portion Sizes and Their Effect on Appetite

SET
Start date: September 15, 2010
Phase: N/A
Study type: Interventional

Investigators are interested in learning how appetite responds to pasta containing different amounts of protein and fiber when provided in two different portion sizes. In this research study, subjects will be asked to eat an entire pasta serving containing different amounts of protein and fiber mixtures. Subjects will be asked to do this on six separate occasions. One time subjects will not receive pasta, only water. After the pasta serving, there will be a buffet of deli style lunch items and subjects may eat as much they desire. Thereafter subjects will describe their feelings of hunger, fullness and desire to eat for 3 hours. In addition, blood will be taken throughout the study period to determine how eating pasta servings in different portion sizes impacts certain hormones released from the intestine, and therefore how they influence appetite. All study visits will take approximately 4 ½ - 5 hours.

NCT ID: NCT01145963 Completed - Appetite Clinical Trials

Pasta Formulations and Their Effect on Appetite

SAT
Start date: June 1, 2010
Phase: N/A
Study type: Interventional

Investigators are interested in learning how appetite responds to pasta containing different amounts of protein and fiber. In this research study, subjects will be asked to eat as much as they want of pasta containing different amounts of protein and fiber mixtures, thereafter subjects will describe their feelings of hunger, fullness and desire to eat for 3 hours afterwards. Subjects will be asked to do this on three separate occasions.

NCT ID: NCT01102907 Completed - Appetite Clinical Trials

Effect of Food Form on Satiety and Gastric Emptying

Start date: May 2010
Phase:
Study type: Observational

Our objective is to determine whether food form (liquid vs. solid) alters gastric emptying, satiety, and food intake, when all macronutrients and fiber are controlled. The study population will include 10 healthy women, who have a normal body mass index. We have chosen to evaluate only women because this is a small pilot study and one of our endpoints is gastric emptying. Gastric emptying is known to differ between men and women. Gastric emptying will be evaluated using the Smartpill technology, satiety will be evaluated using computerized visual analog scales/questions, and food intake will be measured by providing subjects with an ad libitum/buffet-style lunch. Our hypothesis is that our subjects will be less hungry after they eat a solid breakfast compared to a liquid breakfast. We also hypothesize that our subjects will have a slower gastric emptying time after they eat the solid meal. Lastly, we think subjects will want to eat less food at lunch time if they have eaten a solid meal compared to a liquid meal for breakfast.

NCT ID: NCT01029236 Completed - Appetite Clinical Trials

Evaluation of Metabolism-Boosting Beverages

Start date: June 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the effect of Metabolism-boosting Beverages (MBB) containing green tea extract with a standardized amount of epigallocatechin gallate (EGCG) and caffeine.

NCT ID: NCT01006343 Completed - Weight Loss Clinical Trials

Dietary Pork, Appetite and Weight Loss in Human

Start date: n/a
Phase: N/A
Study type: Interventional

The entire study protocol will last 13 weeks. Women will be randomly assigned to one of two experimental groups: high and low protein. All women will consume their unrestricted habitual diet during week 1 while baseline testing and measurements are taken. Starting at week 2, women in both groups will be counseled to consume a 750 kcal/day energy deficit diet containing either the RDA (LP group) or more than the recommended dietary allowance (RDA) (HP group) for protein. The energy restriction period will continue for 12 weeks (through study week 13) and is expected to result in body weight reduction of approximately 17 pounds. Testing and measurements will be repeated during week 13.

NCT ID: NCT01005563 Completed - Weight Loss Clinical Trials

Effects of Dietary Protein Intake From Beef/Pork and Soy/Legumes on Appetite, Mood, and Weight Loss

Start date: January 2010
Phase: N/A
Study type: Interventional

The primary aims of this study are to assess the effects of habitual dietary protein intakes across the acceptable macronutrient distribution range with lean beef/pork or soy/legumes as the predominate sources of protein on indices of daily appetite and mood, and on postprandial appetite, mood, energy expenditure, and glycemic responses during energy-restricted weight loss in overweight adults.