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Weight Loss clinical trials

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NCT ID: NCT02559479 Recruiting - Obesity Clinical Trials

A Study to Assess the Effect of a Normal vs. High Protein Diets in Carbohydrates Metabolism in Obese Subjects With Diabetes or Prediabetes

Start date: September 2015
Phase: N/A
Study type: Interventional

The objective of the study is to assess the effect of low-calorie diets with normal (18%) vs. high (35%) protein (mainly coming from animal source) composition on body weight and carbohydrates metabolism in overweight and obese subjects with pre-diabetes or diabetes. A dietary intervention is carried out during 6 months in 100 subjects who are individually randomized to an energy-restricted diet with two types of macronutrients composition: 1) 35% protein, 30% fat and 35% carbohydrates and 2) 18% protein, 30% fat and 52% carbohydrates. Around 80% of total protein in diet comes from animal source (of whom around 40% from lean red meat). Subjects are provided with weekly menus and different recipes to use them as part of the diet. Monitoring visits with the nutritionist will be performed every 15 days. At the beginning of the study, after 3 and 6 months, the following parameters are determined: anthropometric (weight, waist circumference, body mass index and body composition), blood pressure, dietary (72-hours dietary registry) and exercise and biochemical analysis (total cholesterol, triglycerides, HDL cholesterol, LDL cholesterol, apolipoproteins A1 and B, iron, transferring, ferritin, uric acid, glucose, HbA1c, insulin, adiponectin and resistin). Urine samples are also collected to assess microalbuminuria and ureic nitrogen.

NCT ID: NCT02493140 Recruiting - Weight Loss Clinical Trials

Evaluation of Efficacy of a Cashew Apple Extract on Weight Management and Associated Metabolic Risk Factors in Overweight/Obese Volunteers

Start date: July 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the efficacy and safety of a cashew apple extract on weight management and associated metabolic risk factors in overweight/obese volunteers, versus placebo, after 12 weeks of treatment.

NCT ID: NCT02136173 Recruiting - Weight Loss Clinical Trials

Study of Weight Loss Effect of the Sequential Balloons

Start date: December 2012
Phase: N/A
Study type: Interventional

The effect of the balloon on weight loss is investigated by multiple studies. However, the effect of the sequential balloons is not studied yet.

NCT ID: NCT02129296 Recruiting - Weight Loss Clinical Trials

Intragastric Balloon, Air Versus Fluid Filled: Randomized Prospective Study

Start date: September 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Gastric balloons are an evolving way of reducing weight. There are two types on the market, up to date. Air filled balloons seem to be more safe, and more tolerable.

NCT ID: NCT02052115 Recruiting - Breast Cancer Clinical Trials

Behavioral Weight Loss and Exercise After Treatment (BEAT)

BEAT
Start date: January 2014
Phase: N/A
Study type: Interventional

Overweight and physically inactive breast cancer survivors are at increased risk of breast cancer recurrence and mortality. Cancer treatment-related changes that likely mediate weight loss and exercise success include the long term effects such as fatigue, psychological distress and impaired executive (cognitive) function. This study will explore the variability in how breast cancer survivors respond to a behavioral weight loss intervention. The primary objectives include determining the degree to which success with a behavioral weight loss intervention in overweight breast cancer survivors is explained by measures of executive function as measured with task performance at 6 and 12 months and associated brain function imaging (fMRI), collected at baseline only.Additionally, the study is designed to determine the degree to which selected measures of cancer-related symptoms account for variance in the success of breast cancer survivors at 6 and 12 months following entry into a behavioral weight loss and exercise intervention.

NCT ID: NCT02043457 Recruiting - Obesity Clinical Trials

Identification of Phenotypic Factors That Predict Success for Weight Loss and Long-term Weight Maintenance

Start date: August 2009
Phase:
Study type: Observational

The Investigational Weight Management Clinic now entitled the Weight Management Program at the University of Michigan was created to identify strategies that will result in cost-effective, long term weight management for overweight and obese individuals. The driving hypothesis of the clinic is that the 'one size fits all' philosophy is untenable with a complex disease such as obesity. The clinic will serve as a portal for patients to choose standard clinical care or to explore alternatives from a variety of clinical studies offered through the clinic. These studies will include further investigations into nutrition, the biological basis of weight and weight management and protocols using approved and experimental pharmaceuticals as well as technologies that aid in self-management of weight.

NCT ID: NCT01927783 Recruiting - Obesity Clinical Trials

Heart Health Study in Washington D.C. to Develop a Community-Based Behavioral Weight Loss Intervention

Start date: February 8, 2014
Phase:
Study type: Observational

Background: - Past studies suggest that the best way to improve heart health in the Black community is through community-based programs. Researchers will partner with DC community leaders. They will collect information about the health and health needs of people in mostly Black churches in DC. They will study things that affect heart health, like diabetes, blood pressure, cholesterol, and weight. They will also study how technology can keep track of activities and health. The information will show the health needs of this church-based community. Objectives: - To create an intervention for future programs to improve heart health in African-American churches in Washington, DC. Eligibility: - Adults ages 19 to 85 who attend one of the study churches. Design: - Participants will visit their church for a 4-hour health exam. They will have their blood pressure and body measurements taken. They will have a drop of blood taken from their finger with a small needle. This blood will be tested for blood sugar and cholesterol. Participants will be given the results of these tests. - Participants will answer questions about their health. - All participants will be given an activity monitor to wear for 1 month. The activity monitor is worn around the wrist. Some participants will also receive an activity monitor that is worn around the waist. Participants will be given instructions on how to wear the activity monitors and follow the results on a website. - At the end of 1 month, participants will return one device (they can keep the other). They may receive a gift card for completing the study.

NCT ID: NCT01859013 Recruiting - Obesity Clinical Trials

Topiramate in Adolescents With Severe Obesity

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

The prevalence of severe pediatric obesity is on the rise and youth with this condition are at elevated risk for developing chronic diseases such as cardiovascular disease (CVD) and type 2 diabetes mellitus (T2DM). Topiramate, a medication approved by the Food and Drug Administration (FDA) for the treatment of seizures in adults and children, is associated with weight loss. Although not FDA approved for the treatment of obesity, studies in obese adults have demonstrated weight reduction of approximately 5% with 6-12 months of therapy. However, the weight loss effect of topiramate has never been evaluated among children and adolescents. Therefore, the goal of this pilot study is to evaluate the safety and efficacy of 24 weeks of topiramate therapy with a 4-week run-in of meal replacement therapy in adolescents with severe obesity. The primary hypothesis is that 4 weeks of meal replacement therapy followed by 24 weeks of topiramate will have a larger average percent decline in BMI between baseline and 28 weeks compared to meal replacement therapy followed by placebo.

NCT ID: NCT01844128 Recruiting - Weight Loss Clinical Trials

The Effect of Weight Loss on Ovarian Reserve

Start date: May 2013
Phase: N/A
Study type: Observational [Patient Registry]

Obesity affects on fertility. Obese women have lower pregnancy rate after infertility treatments.They need more doses of hormone during ovarian stimulation, more days for stimulation. During IVF treatment less oocytes are collected and the quality of embryo also harmed. The first line treatment for those women with obesity and infertility is weight loss. The investigators' hypothesis is that weight reduction improves ovarian reserve and fertility treatment outcome.

NCT ID: NCT01773382 Recruiting - Proteinuria Clinical Trials

The Effects of Weight Reduction in IgA Nephropathy

WeightPro
Start date: October 2012
Phase: N/A
Study type: Interventional

The study aims to explore the non-pharmacological treatment of IgA nephropathy by weight reduction. The investigators hypothesized that benefits of weight loss may reduce proteinuria.