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Overweight clinical trials

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NCT ID: NCT02287779 Completed - Clinical trials for Non-Alcoholic Steatohepatitis

Safety and Tolerability Study of SHP626 in Overweight and Obese Adults

Start date: January 19, 2015
Phase: Phase 1
Study type: Interventional

This study will investigate the safety and tolerability of daily dosing regimens of SHP626 in overweight and obese adults.

NCT ID: NCT02283151 Completed - Overweight Clinical Trials

The Effects of a Very Low Carbohydrate Diet Intervention on Weight Control in Overweight/Obese Patients in China

Start date: June 2013
Phase: Phase 2
Study type: Interventional

The study was designed to investigate the effects of a very low carbohydrate diet (VLCD) intervention on weight control in overweight/obese patients in China.All the subjects were randomly assigned to experiment group and control group. The experimental group was given individual instructions on how to follow the VLCD (very low carbohydrate diet). The control group was given an energy-restricted diet.The energy-restricted diet (ER diet) was designed in the traditional Chinese style with an initial target for a total energy intake of 1200 kcal/d (5021 kJ/d).

NCT ID: NCT02283047 Completed - Hypertension Clinical Trials

Effects of Different Aerobic Exercise Programs With Nutritional Interventions in Hypertensive and Overweight People

EXERDIET-HTA
Start date: January 2015
Phase: N/A
Study type: Interventional

Obesity and arterial hypertension (HTN) frequently coexist in the same patient. Moreover, the concept that obesity and HTN can be additive in terms of cardiovascular rist is widely accepted. Yet, clinical decision-making in obese patients is complicated by a surprising lack of evidence on the relative importance of obesity and HTN treatment and its efficacy and safety. Lifestyle interventions are the mainstay of obesity management programs and are also advocated in the prevention and treatment of HTN. Physical exercise and diet are recommended to prevent and control obesity and HTN. Aerobic exercise is firmly established as an effective measure for lowering blood pressure and reducing cardiovascular risk. However, there is no agreement about the optimal dose of frequency, intensity, duration and type of exercise. Therefore, the aims of the study are: 1) to assess the changes in selected parameters of blood pressure, cardiorespiratory fitness, body composition and biological markers brought about by a period of 16-week of different aerobic exercise programs with hypocaloric diet for overweight or obesity and primary hypertensive adults, and 2) to examine the effect of six months detraining subsequent to intervention. Secondary objectives are to examine the additional effect of the intervention on physical activity behavior and health-related quality of life.

NCT ID: NCT02281253 Completed - Overweight Clinical Trials

Effects of a Bakery Product Enriched With Fibre and L-carnitine on Insulin Resistance in Patients With Metabolic Syndrome

Start date: April 2010
Phase: N/A
Study type: Interventional

The aim of this study was to evaluate the efficacy of a bakery product enriched with dietary fibre and L-carnitine on glucose homeostasis and insulin sensitivity in overweight patients with or without metabolic syndrome.

NCT ID: NCT02280772 Completed - Obesity Clinical Trials

Effect of Glucomannan Supplementation on Body Weight in Overweight and Obese Children

Start date: April 27, 2015
Phase: Phase 4
Study type: Interventional

Glucomannan (GNN), a water-soluble dietary fiber derived from the plant Amorphophallus konjac, is marketed for weight reduction. The exact mechanisms by which GNN might exert its actions are unclear. Nonetheless, it has been shown that GNN slows gastric emptying by forming a viscous gel of large volume, which increases the feeling of satiety. Current evidence on the effectiveness of GNN for weight reduction is sparse, and well-designed trials performed in children are needed to assess the efficacy of this modality. We aim to systematically evaluate the efficacy of GNN consumption for the management of overweight and obesity in children.

NCT ID: NCT02278939 Completed - Overweight Clinical Trials

Fit and Trim for Diabetes Prevention

Start date: November 2014
Phase: N/A
Study type: Interventional

Filipino Americans (FA) are the second largest (3.4 million) Asian group in the US. and have one of the highest prevalences of obesity and type 2 diabetes mellitus compared to non-Hispanic whites, African Americans and Hispanics. However, FA have been underrepresented in health related research, particularly in diabetes prevention. This proposed pilot study is the first clinical trial to assess preliminary estimates of the short-term effect of the novel social networking diabetes prevention program lifestyle intervention for this high-risk population.

NCT ID: NCT02278705 Completed - Overweight Clinical Trials

Primary Care Clinical Practice Elements and Improving Overweight Children's Weight Status

Start date: January 2009
Phase:
Study type: Observational

The purpose of this study is to identify whether specific clinical practices—including attention to body-mass-index (BMI) screening/overweight/obesity, medical risk (from conditions associated with overweight/obesity such as high blood pressure), and following up to reassess progress—will improve the weight status of overweight school-age children.

NCT ID: NCT02277899 Completed - Overweight Clinical Trials

Primary Care, Communication, and Improving Children's Health

Start date: October 14, 2014
Phase:
Study type: Observational

The purpose of this study is to determine communication content and strategies in primary care that predict improvement in weight status among overweight school-age children.

NCT ID: NCT02277496 Completed - Obesity Clinical Trials

Wellness Program Implementation: School & Student Toolkits

Start date: July 2013
Phase: N/A
Study type: Interventional

The project is designed to evaluate a participatory implementation model in HealthCorps (HC) high schools and to assess outcomes within and across school settings . The behavioral objectives from the 2010 Dietary Guidelines to address obesity in youth include: 1) decreasing sugary beverage intake; 2) increasing frequency of breakfast; 3) increasing vegetable and fruit intake to 2½ cups per day;4) decreasing frequency of fast food meals;5) becoming physically active (goal of 1 hour per day); and 6) reducing sedentary behavior time (<2 hour day). The study is employing system dynamics modeling (SDM) to assess wellness programming options and to evaluate the program implementation within the context of diverse school ecologies. The RE-AIM evaluation metric (Reach, Effectiveness, Adoption, Implementation, and Maintenance) is used to guide SDM development and validation. The Specific Aims are: 1. To use PAR (Participatory Action Research) methods to refine the school wellness program model and toolkit components that address institutional/community level program implementation barriers and individual level barriers to achieving healthy lifestyle recommendations. 2. To assess the effectiveness of program components using process evaluation techniques guided by the RE-AIM (Reach, Effectiveness, Adoption, Implementation, and Maintenance) model. 3. To evaluate implementation with system dynamics modeling to facilitate dissemination. The simulation analysis will apply the RE-AIM framework to address: Reach (participation rates), effectiveness (outcomes), adoption (acceptability), implementation (intervention fidelity), and maintenance (sustainability of lifestyle changes by students and programs by schools), in order to facilitate refining the toolkits and training program for dissemination to other school setting and diverse educational venues.

NCT ID: NCT02276677 Completed - Clinical trials for Overweight and Obesity

Oxytocin Effects on Food Motivation Pathways

Start date: October 2014
Phase: Early Phase 1
Study type: Interventional

Oxytocin is a peptide hormone produced in the brain that regulates food intake. However, the mechanisms for this effect in humans is not yet clear. In this study, the investigators will therefore examine the effect of a single dose of intranasal oxytocin (compared to placebo) on levels of appetite-regulating hormones and functional magnetic resonance imaging activation of areas of the brain involved in food motivation.