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Overweight clinical trials

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NCT ID: NCT01329822 Completed - Type 2 Diabetes Clinical Trials

Effects of Caloric Restriction on Fetuin-A and Cardiovascular Risk Factors

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

The aim of this randomized controlled study was to evaluate the effects of CR on circulating fetuin-A levels in obese humans with type 2 diabetes based on monitoring energy intake and energy expenditure by daily activity. Furthermore, the investigators examined the relationship between the changes of fetuin-A levels induced by CR and cardiovascular risk parameters including atherogenic lipid profile, visceral fat area (VFA), brachial artery endothelial function, and carotid IMT.

NCT ID: NCT01327976 Active, not recruiting - Obesity Clinical Trials

ReCharge Clinical Trial

ReCharge
Start date: May 2011
Phase: Phase 3
Study type: Interventional

To determine the safety and efficacy of the Maestro RC2 System in producing weight loss in obese subjects.

NCT ID: NCT01325805 Terminated - Overweight Clinical Trials

Efficacy of a Structured Weight Loss Program in Overweight Women With a History of Recurrent Pregnancy Loss

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

Overweight and obesity has been associated with a number of adverse pregnancy outcomes in women of reproductive age, including infertility and early pregnancy loss. Recent data suggests that overweight and obese patients are also at increased risk of recurrent pregnancy loss (RPL), a devastating condition that affects 1% of the fertile population. The investigators propose a prospective, randomized controlled trial in which overweight and obese patients with unexplained recurrent pregnancy loss are enrolled in a structured, 6 month, weight loss program or provided routine counseling regarding the importance of weight loss. Pregnancy outcomes will then be followed to assess miscarriage rates. Metabolic outcomes, such as lipid and glucose profiles, will also be evaluated.

NCT ID: NCT01325376 Active, not recruiting - Obesity Clinical Trials

PH iWell Study to Compare an Online Interactive Technology to Self-directed Care in Overweight or Obese Individuals

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

This is a six month lifestyle management study to compare the effects of iWell; a dynamic online interactive technology to a self-directed program in overweight or obese individuals. The primary aim is to test the hypothesis that dynamic online interactive technology intervention is more effective than self-directed program in obtaining and maintaining weight loss and other biometric improvements.

NCT ID: NCT01324973 Completed - Obesity Clinical Trials

Web-Based Weight Management for Individuals With Mental Illness

eWellness
Start date: March 2012
Phase: N/A
Study type: Interventional

Obesity and physical inactivity have become serious problems for individuals with mental illness, resulting in increased rates of chronic disease, premature death, and substantial health care costs. Although in-person psychoeducational interventions help individuals with mental illness manage their weight, these interventions are often not used because they require frequent travel to treatment programs and substantial time from clinicians. This project addresses these barriers by developing and evaluating the effectiveness of an web-based computer system that is focused on diet and exercise education, and designed to help individuals with mental illness manage their weight.

NCT ID: NCT01323283 Completed - Clinical trials for Overweight and Obesity

Study of Omega-3 Fatty Acids Regarding Ergogenic, Anti-inflammatory and Obesity Inhibitory Effects in 8 Year Old Children

STOPP-8 OM3
Start date: September 2011
Phase: N/A
Study type: Interventional

This study hypothesizes that supplementation of omega-3 fatty acids (OM3) can increase physical activity, inhibit rapid gain in body weight and BMI in both sedentary and normally active 8 year old children. The purpose is secondarily to explore patterns of associations between OM3 supplementation, baseline and follow-up levels in all studied parameters. The study also aims to study if basal levels of OM3 are correlated with physical activity and to study if there is an association between basal levels of OM3 and the effect of OM3 supplementation on physical activity. To study if there is an effect of OM3 supplementation on triglyceride and LDL cholesterol levels and to study if there are more pronounced effects on children with higher levels. To study if OM3 supplementation, compared with placebo reduce weight increase among children at risk to become overweight. To study if there is an association between effects of OM3 on physical activity, weight and risk markers in blood. To study if there are any gender differences.

NCT ID: NCT01320722 Completed - Obesity Clinical Trials

Study of Vitamin D and Uric Acid Lowering on Kidney and Blood Vessel Function

MODERATE
Start date: March 2011
Phase: N/A
Study type: Interventional

The investigators hypothesize that, among non-hypertensive overweight and obese individuals, treatment of vitamin D deficiency and lowering uric acid concentrations (by either xanthine oxidase inhibition or increased renal excretion) will attenuate renin angiotensin system (RAS) activation, improve endothelial function, and lower blood pressure.

NCT ID: NCT01320189 Completed - Obesity Clinical Trials

Dietary Protein Requirements on Unbalanced Diets

Start date: May 2011
Phase: N/A
Study type: Interventional

The objective of this study is to determine ad libitum daily energy and protein intake, energy balance and appetite profile in response to protein/carbohydrate and fat ratio over 12 consecutive days, also as a function of age, gender, BMI and FTO polymorphisms.

NCT ID: NCT01317524 Completed - Inflammation Clinical Trials

The Effects of Homogenized and Unhomogenized Milk on Postprandial Metabolism in Healthy Overweight Men

Start date: February 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effects of homogenized, unhomogenized and skimmed milk on postprandial metabolism in healthy overweight men

NCT ID: NCT01317290 Completed - Overweight Clinical Trials

Supplementation of Alpha-linolenic Acid (ALA)-Rich Oil in Humans

ALA_KK
Start date: February 2012
Phase: Phase 0
Study type: Interventional

The objective of this study is to investigate the accumulation of n-3 LC-PUFA (EPA, DPA and DHA) in human lipids by oral supplementation of ALA-rich linseed oil. In addition, the accumulation of n-3 LC-PUFA is compared between subpopulations of different age, gender and physiological conditions (overweight, increased serum total cholesterol).