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Overweight clinical trials

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NCT ID: NCT00403689 Completed - Overweight Clinical Trials

Effects of (1,3), (1,6)-Beta-D-glucan on Insulin Sensitivity and Inflammatory Markers of the Metabolic Syndrome

Start date: November 2006
Phase: N/A
Study type: Interventional

Insoluble (1,3),(1,6)-beta-D-glucan from bakers yeast are indigestible polysaccharides. Previous studies indicate that the intake of insoluble dietary fiber is strongly associated with reduced risk of type 2 diabetes and cardiovascular disease. However, the mechanisms leading to this phenomenon are largely unknown. There are close relations between metabolic and inflammatory pathways, and a number of hormones, cytokines, signal proteins, bioactive lipids, and transcription factors have been shown to be involved in both systems. Beta-D-glucans have been suggested to play a role as so called biological response modifiers. Studies in animals indicate that even small doses of (1,3),(1,6)-beta-D-glucan may have beneficial effects on immune activity, i.e., by reducing the secretion of inflammatory factors. The investigators hypothesize that the intake of isolated (1,3), (1,6)-beta-D-glucan from bakers yeast improves inflammatory makers and insulin-sensitivity in overweight subjects with increased C-reactive protein concentrations at baseline.

NCT ID: NCT00402077 Completed - Obesity Clinical Trials

A Study to Examine the Safety, Tolerability, and Body Weight Effect of Pramlintide Alone and in Combination With Oral Antiobesity Agents in Overweight and Obese Subjects

Start date: November 2006
Phase: Phase 2
Study type: Interventional

This study will examine the safety, tolerability, and body weight effect of subcutaneous pramlintide alone and in various combinations with the oral antiobesity agents sibutramine or phentermine in overweight and obese subjects.

NCT ID: NCT00397865 Completed - Obesity Clinical Trials

A Primary Care Educational Intervention for Families of Overweight Children

Start date: October 2006
Phase: N/A
Study type: Interventional

The purpose of the research is to find out if an educational booklet is helpful to families with overweight children. The educational booklet contains information for parents about nutritious eating, physical activity, and strategies for healthy living.

NCT ID: NCT00395135 Completed - Obesity Clinical Trials

BLOOM: Behavioral Modification and Lorcaserin for Overweight and Obesity Management

Start date: November 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the weight loss effect of lorcaserin at the end of the first year of treatment (Week 52) and to assess the ability of lorcaserin to maintain weight loss at the end of the second year of treatment (Week 104)

NCT ID: NCT00392925 Completed - Obesity Clinical Trials

A Study to Evaluate the Effect on Body Weight of Leptin Administered in Conjunction With Pramlintide in Overweight and Obese Subjects

Start date: October 2006
Phase: Phase 2
Study type: Interventional

This study will evaluate the safety, tolerability, and effect on body weight of leptin, injected subcutaneously, in combination with pramlintide, injected subcutaneously.

NCT ID: NCT00386672 Completed - Obesity Clinical Trials

Calcium Supplementation for a Healthy Weight-Lite (CaSHeW Lite)

Start date: May 2006
Phase: N/A
Study type: Interventional

The purpose of the study is to find out if taking calcium and vitamin D supplements, while following a low-calorie diet, can help people lose weight.

NCT ID: NCT00382473 Terminated - Clinical trials for Diabetes Mellitus, Type 2

Mitochondrial Dysfunction in Type 2 Diabetes Mellitus and Capacity for Fat Oxidation During Exercise

Start date: September 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effects of an 8-week aerobic training program upon fat oxidation in vivo and markers of skeletal muscle mitochondrial content and oxidative capacity in sedentary obese subjects with and without type 2 diabetes. We will also investigate if mitochondrial content in muscle predicts success of weight loss. The specific aims are: - To compare systemic fat oxidation rates; - To measure mitochondrial content in muscle before and after aerobic training; - To determine if decreased mitochondrial content is also associated with decreased mitochondrial oxidative capacity; - To measure non-plasma fatty acid oxidation in vivo during submaximal exercise conditions both prior and after aerobic training; - To determine whether increases in fat oxidation due to physical activity predict weight loss success when a reduced calorie diet is added to a physical activity program.

NCT ID: NCT00381160 Completed - Obesity Clinical Trials

Reducing Sugar-sweetened Beverage Consumption in Overweight Adolescents

BASH
Start date: September 2006
Phase: N/A
Study type: Interventional

The primary aim of this study is to examine the effect of a multi-component intervention, designed to reduce consumption of sugar-sweetened beverages, on weight gain, total energy intake, and diet quality in adolescents. The secondary aim is to evaluate whether outcomes of the intervention differ between adolescents for whom 100% fruit juice vs. other products (i.e., soda, fruit punch, lemonade, iced tea, coffee drinks, energy drinks, sports drinks) constitutes the primary source of sugar from beverages.

NCT ID: NCT00377767 Recruiting - Clinical trials for Risk of Overweight in Preschool Age Children

Improving Primary Care to Prevent Childhood Obesity

Start date: September 2006
Phase: Phase 1/Phase 2
Study type: Interventional

To determine the extent to which a clinical intervention based on the Chronic Care Model (CCM), compared with the usual care control condition, results in a smaller age-associated increase in body mass index (BMI) over a 1 year intervention (primary outcome) and a 1 1/2-year follow-up period.

NCT ID: NCT00377026 Completed - Obesity Clinical Trials

FirstWIND: Weight Loss Interventions After Delivery

Start date: September 2006
Phase: N/A
Study type: Interventional

This a pilot intervention study in which postpartum women will be randomized to receive a 6-month postpartum weight loss intervention or usual care.