Clinical Trials Logo

Overweight clinical trials

View clinical trials related to Overweight.

Filter by:

NCT ID: NCT00458224 Completed - Obesity Clinical Trials

Prevention of Permanent Obesity in Children

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

In the county of Oppland, Norway, questionnaires addressing physical and mental health and socioeconomic status is issued to all (1960) families who meet for the pre-school assessment at the public health clinics in 2007. Particularly growth, physical activity and diet is addressed. Families who have children with a BMI >18.9, which corresponds to BMI>30, and living in selected municipalities in the county are invited to participate in a 5 year intervention program in order to avoid future overweight conditions in children. Similarly overweight children from the rest of the county serve as controls.

NCT ID: NCT00456521 Completed - Obesity Clinical Trials

A Safety and Efficacy Study of Naltrexone SR/Bupropion SR and Placebo in Overweight and Obese Subjects Participating in an Intensive Behavior Modification Program

Start date: March 2007
Phase: Phase 3
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 treating obesity and leads to greater weight loss when given with a group lifestyle modification program than with group lifestyle modification alone.

NCT ID: NCT00455780 Completed - Obesity Clinical Trials

Weight Loss Maintenance in Primary Care

PrimaryCare
Start date: January 2005
Phase: N/A
Study type: Interventional

After a three month weight loss phase involving the use of meal replacements, participants are randomized into different weight loss maintenance conditions. Aim 1: To test the hypothesis that the meal replacement (MR) and reduced energy density eating (REDE) interventions, when added separately to the LEARN program, will produce superior weight loss maintenance compared to a LEARN-only intervention. Aim 2: To test the hypothesis that the weight loss maintenance condition that combines MRs and REDE will produce better maintenance of weight losses than either individual component and than the LEARN-only condition. Aim 3: To test the hypothesis that the two conditions receiving the REDE intervention will experience longer-lasting improvements in the energy density and nutritional composition of the diet compared to the two non-REDE conditions.

NCT ID: NCT00455403 Completed - Hypertension Clinical Trials

Atheroma Reduction With Chloroquine in Patients With the Metabolic Syndrome (ARCH-MS)

ARCH-MS
Start date: April 2006
Phase: N/A
Study type: Interventional

Metabolic syndrome consists of a group of co-occuring conditions that increase an individual's risk of developing heart disease, stroke, and diabetes. The purpose of this study is to evaluate the long-term effectiveness of chloroquine, a protein-activation medication, at reducing the progression of atherosclerosis in patients with the metabolic syndrome. Sub-study: Vascular endothelial growth factor(VEGF)and Cardiometabolic Risk, The purpose is to determine if the association of VEGF with atherosclerosis indicates that it should be a marker of the disorder.

NCT ID: NCT00455325 Completed - Hypertension Clinical Trials

Chloroquine to Treat People With Metabolic Syndrome Aim2 (ARCH-MS)

ARCH-MS
Start date: September 2004
Phase: Phase 2
Study type: Interventional

Metabolic syndrome consists of a group of co-occuring conditions that increase an individual's risk of developing heart disease, stroke, and diabetes. The purpose of this study is to evaluate the short-term effectiveness of chloroquine, a protein-activation medication, at improving metabolic syndrome.

NCT ID: NCT00454610 Completed - Obesity Clinical Trials

Family Lifestyle Overweight Prevention Program

FLOW
Start date: January 2005
Phase: Phase 3
Study type: Interventional

The purpose of the study was to design a weight management program for Mexican American youth and to determine the effectiveness of the program for weight management compared to a self help program. 1. At the end of 6 months, individuals randomly assigned to Intensive Intervention (II) (instructor/trainer led intervention) will lose more weight than individuals assigned to Self Help (SH) only. 2. At the end of 1 year, individuals randomly assigned to II will maintain their weight losses better than individuals assigned to SH. Secondary hypotheses will include examination of main effects and interactions at the end of 6 months with the following secondary dependent measures: treatment adherence (e.g., attendance, food diaries, exercise diaries), blood levels, changes in percent body fat, overall psychological functioning (PEDS-QL 4.0), and eating behaviors as assessed by food frequency checklists.

NCT ID: NCT00447291 Terminated - Obesity Clinical Trials

Safety & Efficacy of Omega-3 Fish Oil in Overweight Children & Adolescents

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

Children with an excess in body weight, increase the risk of obesity-related co-morbidities and cardiovascular diseases. Childhood obesity may be due to diets laden with fat and lack of physical activity. Omega-3 fish oil is a supplementation that may promote a greater reduction of pro-inflammatory mediators; combined with exercise and nutritional regimens it may also help improve glycemic, lipid markers, and body composition in overweight children and adolescents.

NCT ID: NCT00445627 Completed - Obesity Clinical Trials

Effect of Short-Term Beta-Cell Rest in Adolescents and Young Adults With Type 2 Diabetes Mellitus

Start date: June 18, 2007
Phase:
Study type: Observational

This study will determine whether resting beta cells (cells in the pancreas that produce insulin) for 2 weeks will improve the ability of patients with Type 2 diabetes mellitus (T2DM) to make insulin. Beta cells can rest by giving patients insulin shots. The study will also examine how teenagers with T2DM feel about having diabetes and explore differences between young people with and without T2DM. This study includes patients 12 to 25 years of age with T2DM who are overweight and who were diagnosed within 2 years of enrolling in the study. Healthy individuals of normal weight or who are overweight are also eligible. Candidates are screened with a medical history, physical examination and laboratory tests. Participants with T2DM are assigned to one of two groups. Group 1 takes an anti-diabetes medicine called metformin and follows a diet prescribed by a study staff dietitian for 2 weeks. Group 2 takes metformin, follows the prescribed diet, and receives insulin through a pump under the skin for 2 weeks. During these two weeks, all participants have the following tests: - Frequent blood sugar checks. - Oral glucose tolerance test (routine diabetes test in which blood samples are drawn before and several times after the subject drinks a sugary solution). - Arginine stimulation to test the response of the body to arginine, a normal ingredient of food that stimulates the release of insulin. Two catheters are placed into veins in the arms, one to administer a liquid containing arginine, the other to draw the blood samples. - Ultrasound of the blood vessels in the neck to check for hardening of the arteries. - Metabolism test to measure the amount of oxygen used during rest. The subject breathes normally during rest while wearing a canopy over his or her head for about 20 minutes. - MRI scans of the abdomen to examine the amount of fat in the belly (at the beginning and end of the study) - DEXA scan to determine percent body fat. - Tests to explore quality of life and feelings about health, work or school, friends and family. - Exercise testing on a treadmill or stationary bicycle. - Genetic studies for information on diabetes and obesity. Normal volunteers have blood draws, oral glucose tolerance testing, MRI scan, DEXA scan, psychological testing, exercise testing, and genetic testing. ...

NCT ID: NCT00444561 Completed - Obesity Clinical Trials

Exploratory Study to Evaluate Various Pharmacodynamic Effects of Subcutaneously Infused or Injected Pramlintide in Obese Subjects

Start date: August 2004
Phase: Phase 2
Study type: Interventional

This exploratory study is designed to evaluate various pharmacodynamic effects of subcutaneously (SC) infused or injected pramlintide in obese, nondiabetic male and postmenopausal female (not on hormone replacement therapy) subjects. The study will also assess the safety and tolerability of pramlintide administered by SC infusion or injection.

NCT ID: NCT00438126 Completed - Obesity Clinical Trials

Family-Centered Diabetes Project - Sharing Wisdom

Start date: January 2002
Phase: N/A
Study type: Interventional

This is a randomized trial of an educational intervention to reduce the risk of diabetes among urban American Indian women