Clinical Trials Logo

Abdominal Obesity clinical trials

View clinical trials related to Abdominal Obesity.

Filter by:

NCT ID: NCT00990457 Completed - Overweight Clinical Trials

Evaluating the Effects Two Diets Combined With Exercise in Persons With Abdominal Obesity (The SHAPE5 Study)

SHAPE5
Start date: October 2009
Phase: Phase 3
Study type: Interventional

Abdominal obesity, which is affected by a lack of physical activity and excess weight, put people at an increased risk of cardiovascular disease. This study will compare the effects of two different dietary approaches to weight loss, each combined with exercise, for their effects on cardiovascular factors that are early predictors of future cardiovascular disease in overweight and obese people with excessive weight around their waist. The two diets are a low-carbohydrate versus a more traditional low-fat, low calorie diet.

NCT ID: NCT00940966 Completed - Insulin Resistance Clinical Trials

A Pilot Study to Determine the Efficacy of a Low Carbohydrate Diet in Treatment of Adolescents With Metabolic Syndrome

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

The purpose of this study is to determine the effectiveness of two different non-energy restricted controlled carbohydrate programs with the American Diabetes Associations' diet on glycosylated hemoglobin and other diabetes risk factors in obese adolescents with metabolic syndrome, a constellation of symptoms associated with the development of type 2 diabetes and cardiovascular disease.

NCT ID: NCT00893646 Completed - Abdominal Obesity Clinical Trials

Effects of Weight Reduction on Sleep and Alertness in Long-distance Truck and Bus Drivers

SF-Truck
Start date: May 2009
Phase: N/A
Study type: Interventional

The study is a year-long health-behaviour intervention in obese, male truck-drivers to lose weight moderately by 10%, using monthly individual counseling. The investigators hypothesize that lifestyle modification (increased physical activity, changes in eating habits, and improved schedule for sleep) through weight loss improves daytime alertness and quality of sleep, reduces daytime sleepiness, and improves cardiovascular risk factors and health-related fitness.

NCT ID: NCT00781547 Completed - Obesity Clinical Trials

Growth Hormone Treatment in Men With High Risk of Developing Type 2 Diabetes Mellitus

GHDM
Start date: January 1999
Phase: Phase 3
Study type: Interventional

The overall aim of this study is to investigate the effects of GH treatment in men with the Metabolic Syndrome and a high risk of developing type 2 DM. Forty men with abdominal obesity and impaired glucose tolerance will be randomized to two parallel treatment groups with GH and placebo for 12 months. The subjects will receive treatment with recombinant human GH (Genotropin®) or placebo administered by a daily s.c. injection before bedtime. The initial dose of GH will be 0.4 IU per day increased to 0.8 IU after 2 weeks and to 1.2 IU after 4 weeks of treatment. Thus, the target dose is 1.2 IU per day which resembles approximately 0.015 IU/kg/day. The GH dose will be reduced by half in the event of side-effects. Oral and written instructions in terms of administration and dosage will be given. The treatment can be discontinued by the patient. The treatment should be discontinued if malignancy is discovered, DM developes, if the subject experience a cerebrovascular disease and in the event of any other side-effects that is considered as serious. The treatment code for each subject included in the trial will be kept at the Sahlgrenska University Hospital Pharmacy. This code can be broken on the request of the investigator. Compliance will be assessed by collecting empty vials from the study subjects. The treatment is discontinued at the end of the study.

NCT ID: NCT00739180 Completed - Abdominal Obesity Clinical Trials

Physical Activity in Youth: Implications for Reversing Risk Factors for Type 2 Diabetes

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

In this randomized controlled trial, we will examine the effect of a 3-month exercise training (aerobic exercise versus resistance exercise) without calorie restriction on total and regional adiposity, and risk of type 2 diabetes in overweight children and adolescents.

NCT ID: NCT00675506 Completed - Clinical trials for Growth Hormone Deficiency

Effectiveness of Growth Hormone Releasing Hormone in Reducing Abdominal Fat in People Who Are Obese

Start date: July 2008
Phase: Phase 2
Study type: Interventional

Obesity, a condition that occurs when a person has too much body fat, affects about 31% of people in the United States. It is associated with increased risk of diabetes, high blood pressure, high cholesterol, and cardiovascular disease. Abdominal obesity, in particular, is also associated with low levels of growth hormone, a hormone that affects rate of growth and the way the body uses energy. Growth hormone releasing hormone (GHRH) is a substance that makes the body naturally increase its own growth hormone levels. Administering GHRH to people who are obese may help return their growth hormone levels to normal and, in turn, may lead to reduced abdominal fat and improved cardiovascular function. This study will evaluate the effectiveness of synthetic GHRH in decreasing the amount of abdominal fat and improving cardiovascular function in people who are obese.

NCT ID: NCT00664729 Completed - Metabolic Syndrome Clinical Trials

Diet, Exercise, Metabolism, and Obesity in Older Women

DEMO
Start date: November 2002
Phase: N/A
Study type: Interventional

Reductions in fat oxidation and resting metabolic rate (RMR) are associated with normal aging and are accelerated with menopause. As a result, postmenopausal women have an increased risk of abdominal obesity and ultimately the metabolic complications that lead to the insulin resistance syndrome and its associated risks (hyperlipidemia, type 2 diabetes, and coronary heart disease). Thus, there is a need to determine the most successful treatment to reduce visceral obesity in postmenopausal women. The purpose of this study is to determine if dietary-induced weight loss alone and/or weight loss combined with exercise at low and high- intensities differentially affect the reduction in visceral adipose tissue in postmenopausal women with abdominal obesity.

NCT ID: NCT00655902 Completed - Type 2 Diabetes Clinical Trials

Copenhagen Obesity Risk Assessment Study

COBRA
Start date: April 2008
Phase: N/A
Study type: Interventional

The aim of the present study is to assess the effect of a high intake of industrially produced trans fatty acids for 16 weeks on abdominal obesity and risk markers of type 2 diabetes and heart disease in healthy, moderately overweight, postmenopausal women.

NCT ID: NCT00520858 Completed - Abdominal Obesity Clinical Trials

Effects of Exercise Modality on Abdominal Obesity and Health Risk Factors in Older Men and Women

Start date: September 2003
Phase: N/A
Study type: Interventional

The prevalence of abdominal obesity in the elderly is increasing at alarming rates and thus, requires immediate attention. By comparison to younger adults, obesity reduction in the elderly presents a unique challenge and requires an innovative approach. We propose a novel approach to investigate the effects of different exercise types as independent treatment strategies for the reduction of obesity and related health risk factors in older men and women. We propose that exercise without caloric restriction will be associated with modest weight loss (3-5%), that in turn will be associated with significant reduction in abdominal obesity, insulin resistance, and a corresponding increase in skeletal muscle mass and function. We will determine the separate effects of resistance and aerobic exercise on these primary outcome variables, and, whether a treatment strategy that combines the two is optimal.

NCT ID: NCT00459056 Completed - Hypertension Clinical Trials

The Vascular Effects of Carvedilol Controlled Release (CR) in Abdominally Obese Hypertensive Patients

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

The purpose of this study is to compare the effects of two different combination therapies for high blood pressure on vascular health.