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Overweight clinical trials

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NCT ID: NCT01552642 Completed - Obesity Clinical Trials

An Interactive Web-based Intervention to Achieve Healthy Weight in Young Children

Start date: February 2013
Phase: Phase 3
Study type: Interventional

The overall purpose of this study is to develop and implement an effective intervention program designed to prevent and treat obesity in young children.

NCT ID: NCT01551238 Recruiting - Obesity Clinical Trials

Energy Expenditure, Sleep and Macronutrients

Start date: March 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to determine energy expenditure and sleep in response to protein/carbohydrate and fat ratio of the diet over a short-term and long-term period of time.

NCT ID: NCT01550926 Completed - Overweight Clinical Trials

A Study to Assess the Pharmacologic Equivalence of Two Orlistat Dosage Forms

Start date: February 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine whether a new dosage form and dose of orlistat is equivalent to the currently marketed form.

NCT ID: NCT01550133 Completed - Overweight Clinical Trials

Effects of Food Form on Cephalic Phase Responses

Start date: September 1, 2012
Phase: N/A
Study type: Interventional

This study has two main aims: 1) To determine if ingestion of solid or beverage food forms will change appetite hormone responses, and 2) To determine whether "learning" (defined as 2 week daily consumption) about the metabolic consequence of ingesting solid or beverage foods forms varying in energy alters appetite hormone responses. Beverage consumption has been implicated in the problem of obesity. However, the exact relationship between beverages, lower appetitive response and lower compensatory dietary responses remains unclear. This study aims to address this gap in the research. For aim 1, the null hypothesis is that the energy in beverage and solid forms will not affect appetite hormonal responses differently. The alternative hypothesis is that exposure to the energy-yielding beverage will elicit a lower appetitive hormone response compared to oral exposure to the solid food form. For aim 2, the null hypothesis is that learning will not change appetite hormone responses. The alternative hypothesis is that learning will decrease appetite hormone responses in the non-energy-yielding beverage more than in the energy-yielding beverage.

NCT ID: NCT01549626 Completed - Overweight Clinical Trials

Effects of Flaxseed Flour in Appetite Sensations, Lipid Profile and Pressure Levels Among Overweighed and Obese Women

Start date: March 2009
Phase: N/A
Study type: Interventional

Inclusion of foods rich in fiber, such as flaxseed, is a nutritional strategy for treating obesity. The hypothesis of this study is to compare the effects of three types of flaxseed flour - whole brown flaxseed flour, brown defatted flaxseed flour and golden flaxseed flour in the sensations of appetite and satiety, lipid profile, pressure levels and associated costs in overweight and obese women.

NCT ID: NCT01542671 Completed - Clinical trials for Overweight and Obesity

Tailored Lifestyle Intervention in Obese Adults Within Primary Care Practice - Choose to Lose

CTL
Start date: September 2009
Phase: N/A
Study type: Interventional

The primary objective of the study is to evaluate the effectiveness of tailored lifestyle intervention in primary care by comparing changes in the primary measure of weight and body mass index (BMI) and secondarily: physical activity (PA), fat calories consumed, and fruit/vegetable servings within the two arms (intervention and control) of the study. It is hypothesized that the intervention cohort will demonstrate greater reductions in body weight, body neglect, and fat calories consumed and greater increases in physical activity and fruits/vegetable servings after two years compared to the control cohort. The study also aims to evaluate and compare the cost of intervention for purpose per each unit of measure lost between the two arms of the study as a secondary objective. The cost of intervention will be evaluated as it relates to study replication.

NCT ID: NCT01540864 Terminated - Obesity Clinical Trials

A Safety and Efficacy Study of HPP404 on Weight Loss in Overweight or Obese Subjects

Start date: May 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare the safety and effect of HPP404 versus placebo on body weight in overweight or obese subjects.

NCT ID: NCT01534325 Recruiting - Overweight Clinical Trials

Efficacy Study for SD Device

Start date: July 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the SD unique device is effective in treatment of overweight and obesity.

NCT ID: NCT01534091 Terminated - Obesity Clinical Trials

Enhancing the Amount of Physical Activity Carried Out by Overweight Children at Leisure Time

Start date: May 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to examine if internet supervised by pedometer will contribute to enhance the amount of physical activity at leisure time by obese children. The investigators hypothesize that using pedometer will increase the amount of physical activity done by obese children in the afternoon and will improve the likelihood of success in the intervention program.

NCT ID: NCT01533987 Completed - Clinical trials for Overweight and Obesity

Effects of Juice Plus+® Supplementation on Endothelial Function in Overweight Men

Start date: July 2009
Phase: N/A
Study type: Interventional

The purpose of the study is to determine the effects of daily ingestion of Juice Plus+® capsules containing Orchard, Garden and Vineyard blends on endothelial function and biomarkers of oxidative stress (oxidized LDL, lipid hydroperoxides and protein carbonyls) in overweight men as compared to the placebo group.