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Overweight clinical trials

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NCT ID: NCT00603291 Completed - Obesity Clinical Trials

BLOOM-DM: Behavioral Modification and Lorcaserin for Overweight and Obesity Management in Diabetes Mellitus

Start date: December 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the weight loss effect of lorcaserin during and at the end of 1 year of treatment in overweight and obese patients with Type II diabetes mellitus treated with metformin, sulfonylurea (SFU), or either agent in combination with other oral hypoglycemic agents.

NCT ID: NCT00601653 Completed - Obesity Clinical Trials

Effectiveness of Cognitive Behavioral Therapy Plus Nutritional Counseling in Promoting Weight Loss in People With Binge Eating Disorder

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

This study will evaluate the effectiveness of adding nutritional counseling to cognitive behavioral therapy in treating obese people with binge eating disorder.

NCT ID: NCT00601354 Completed - Overweight Clinical Trials

Adding Guided Self-Help Group Therapy to the Alli Weight Loss Program in Treating Binge Eating Disorder

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

This study will evaluate the effectiveness of adding guided self-help group therapy to a weight loss program in achieving weight loss and reducing binge eating in overweight binge eaters.

NCT ID: NCT00584519 Completed - Schizophrenia Clinical Trials

Control of Metabolic and Cardiovascular Risk in Patients With Schizophrenia and Overweight

CRESSOB
Start date: June 2007
Phase:
Study type: Observational

To analyse the progress of modifiable metabolic risk factors (Blood pressure, cigarette smoking, waist perimeter, BMI, glycemia and lipidic profile) in schizophrenic patients with overweight for 12 months. To analyse the perceived health status and the level of functioning and disability of patients with schizophrenia and overweight and their progress at 3, 6 and 12 months. To assess the progress of the symptoms of the disease at 6 and 12 months.

NCT ID: NCT00579657 Completed - Obesity Clinical Trials

Protein, Fiber, and Metabolic Syndrome - The PROFIMET Study

PROFIMET
Start date: August 2007
Phase: N/A
Study type: Interventional

Randomized controlled single-blinded intervention study in 111 overweight and obese subjects with risk factors of developing type 2 diabetes, with the aim to investigate effects of isoenergetic high cereal fiber as compared with high protein diets over 6 and 18 weeks. Proof of principle study with analysis according to study protocol, investigating whether isoenergetic high cereal fiber and high protein diets with comparable fat contents, if adhered to and after exclusion of known confounders such as changes in body weight, intake of drugs with known effects on insulin sensitivity, or relevant changes in physical activity, indeed affect insulin sensitivity.

NCT ID: NCT00575991 Completed - Overweight Clinical Trials

Effect of Conjugated Linoleic Acid on Body Fat in Overweight Children

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

The prevalence of overweight children has increased dramatically over the last decade, and many overweight children will remain overweight as adults. Conjugated linoleic acid (CLA), a naturally occurring dietary fatty acid, has shown promising results in reducing body fat among adults, and we propose to test the efficacy of CLA supplementation on body fat accretion in 6 to 10 year old children who are overweight or at risk of overweight.

NCT ID: NCT00573482 Completed - Obesity Clinical Trials

A Cafeteria Based Study of Weight Gain Prevention

Cafeteria
Start date: September 2002
Phase: N/A
Study type: Interventional

The dramatic rise in overweight and obesity during the past several decades can be explained by environmental changes that foster increased energy intake and decreased energy expenditure. There are several reasons to suggest that the most effective approach to weight gain prevention is the incorporate reduced-fat eating into an overall strategy of lowering the energy density of the diet. Our energy density manipulations will be designed to reduce both the fat content and the caloric density of foods served at a cafeteria, which serves as the "food environment" for hospital employees.

NCT ID: NCT00567255 Completed - Obesity Clinical Trials

A Safety and Efficacy Study of Naltrexone SR/Bupropion SR in Overweight and Obese Subjects

Start date: December 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether the combination of naltrexone SR and bupropion SR is safe and effective in the treatment of obesity.

NCT ID: NCT00563563 Completed - Obesity Clinical Trials

A Study of Naltrexone SR/ Bupropion SR in Overweight and Obese Subjects Who Are Nicotine-Dependent

Start date: October 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether a combination of naltrexone SR and bupropion SR is safe and effective in the treatment of nicotine-dependence in overweight and obese subjects.

NCT ID: NCT00562263 Completed - Overweight Clinical Trials

Barriers to Effective Weight Loss in Overweight Adolescents

TEENS
Start date: October 2007
Phase: N/A
Study type: Interventional

The current study aims to investigate the impact of a comprehensive, team-based, family-centered, lifestyle modification program on body weight, metabolic abnormalities, fitness measures, and self-esteem in overweight adolescents beginning the study at ages 11-18 years. The intensive program will uniquely include a "team" structure and a component designed to address the role of parental modeling in effective lifestyle changes. By comparing the demographic, psychosocial, and metabolic characteristics of adolescents according to the degree of weight loss, the study will also more fully characterize the barriers that prevent successful participation in an intensive lifestyle modification program.