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Overweight clinical trials

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NCT ID: NCT02737293 Terminated - Obesity Clinical Trials

Whole Egg Intake and the Mediterranean Diet

Start date: April 2016
Phase: N/A
Study type: Interventional

This project will evaluate the daily intake of whole eggs in the Mediterranean Diet (Med Diet). Cholesterol levels are normally related to cardiovascular disease (CVD) risk. Dietary fat and the total diet makeup are well known modifiers of CVD risk. The Med Diet has been shown to decrease blood lipids (fats) and reduce inflammation. Cholesterol intake from eggs may not be as bad as once thought and, in fact, may help to improve the blood lipid (fat) levels. This study is being done to test how the addition of eggs to a Med Diet affects blood lipids and other risk markers for CVD.

NCT ID: NCT02721251 Terminated - Overweight Clinical Trials

Influence of Exercise, Weight Loss, and Exercise Plus Weight Loss on Sleep Apnea

Start date: April 1, 2016
Phase: N/A
Study type: Interventional

Obstructive sleep apnea (OSA) is highly prevalent among Veterans, and is associated with significant mortality and multiple morbidities. Available treatments have had limited effectiveness in treating OSA and alleviating associated morbidity. The investigators' previous research found a reduction in OSA severity of approximately 25% following modest exercise training. That this effect occurred independent of weight loss raises the exciting possibility that exercise combined with weight loss could reduce OSA by at least 50% and have unique health benefits for OSA patients. Following screening and baseline assessments, 90 overweight Veterans ages 18-60 years with OSA will be randomized to one of three 16-week treatments: (1) exercise training; (2) 10 % weight loss; and 3) exercise + weight loss. Changes in OSA and related morbidity will be compared between treatments.

NCT ID: NCT02717247 Terminated - Clinical trials for Overweight, Obesity and Other Hyperalimentation (E65-E68)

Transcranial Random Noise Stimulation in Food Addiction Treatment

tRNS-FA
Start date: February 2016
Phase: N/A
Study type: Interventional

Obesity is worldwide a public health problem. According to World Health Organization (WHO), overweight and obesity are the fifth death risk factor worldwide. At least 2.8 million adults die each year. Food addiction is one of the causes of obesity that may benefit from new therapeutic options.

NCT ID: NCT02703753 Terminated - Obesity Clinical Trials

TOP-mums, for a Healthy Start

Start date: July 27, 2016
Phase: N/A
Study type: Interventional

This study evaluates the effect of a lifestyle intervention for women with a pregnancy wish who have a high risk on perinatal morbidity because of overweight or obesity. Half of the patients will receive the lifestyle intervention while the other half will receive usual care. It is hypothesized that an effective lifestyle intervention directed towards healthy living, including reduction of overweight or obesity and, if applicable, smoking reduction, health problems in mothers and their offspring can be prevented.

NCT ID: NCT02701426 Terminated - Obesity Clinical Trials

Obesity & Pregnancy: Factors Influencing Participation in a Physical Activity and Nutritional Counseling Program

OGAN
Start date: February 2016
Phase: N/A
Study type: Interventional

Background: Obesity increasingly affects young women and contributes to increased maternal, fetal and neonatal complications. Maternal obesity contributes to the subsequent development of childhood obesity not only through social and environmental mechanisms but also through biological processes referring to the original concept of the developmental health and disease. Data suggest that management during pregnancy through nutrition counseling and adequate physical activity will help to break the familial vicious circle of obesity. To help program to be effective it is important to understand the factors that modulate participation. However, few studies have been conducted to assess the determinants that influence participation. Goal: The main objective is to analyze 15 factors that influence participation in a program combining physical activity and nutritional counseling among pregnant women with BMI ≥ 25 kg/m2. Secondary objectives are : - to identify the data that influence adherence and to show that assiduous women will have a better control of weight gain and a reduction of maternal and fetal complications. - to understand the biological mechanisms involved Strategy and method: A prospective research evaluating the participation in an educational program, including nutritional support and adequate physical activity, will be offered to overweight and obese pregnant women. The program will last 12 weeks, and will include three workshops on diet of the pregnant and lactating women, and the young child. Physical activity sessions will be offered once a week. Fifteen independent variables likely to influence participation will be analyzed. The association between participation and the risk of maternal and fetal pregnancy complications related to obesity will be analysed. Meanwhile, more fundamental research will be considered to determine of the biological factors involved.

NCT ID: NCT02674893 Terminated - Type 2 Diabetes Clinical Trials

Effect of Victoza on Dietary Preferences and Habit in Patients With Type 2 Diabetes

GLP1 et Goût
Start date: February 4, 2014
Phase: Phase 4
Study type: Interventional

This is an open-label comparative study in three parallel groups. It is expected that 90 patients and/or healthy volunteers will participate in this biomedical research. Distribution in groups - 30 patients with type 2 diabetes and an indication for treatment with a GLP1 analogue (group 1) - 30 patients with type 2 diabetes (control diabetic subjects) not treated with Incretins (group 2) - 30 healthy subjects (non-diabetics) (group 3) This study will investigate modifications in eating behaviour induced by Liraglutide in patients who start treatment with Victoza® and certain aspects, such as liking (hedonic characteristic of a food), wanting (desire to eat a given food) and salivation in response to the presentation of a food by taking measurements at D0 (before initiation of the treatment with Liraglutide in the group concerned) then at 15 days (except for the controls), 3 months and 9 months (only for controls).

NCT ID: NCT02516397 Terminated - Overweight Clinical Trials

OMNIA Efficacy on Body Fat Mass Reduction

PEPOLUS
Start date: August 2015
Phase: N/A
Study type: Interventional

The purpose of this clinical trial is to evaluate the safety and efficacy of a food supplement OMNIA compared to a placebo in reducing the body fat mass in 70 overweight subjects during 12 weeks treatment.

NCT ID: NCT02356614 Terminated - Obesity Clinical Trials

A Post-approval LAP-BAND® Lower Body Mass Index (LBMI) Study

Start date: March 2015
Phase:
Study type: Observational

This is a post-approval, multicenter, prospective, non-randomized, open-label, clinical study to evaluate the safety and effectiveness of the LAP-BAND® AP System in a lower obese population (BMI ≥ 30 kg/m2 and < 40 kg/m2) with one or more obesity-related comorbidity up to 10 years after implantation. The reason your study has been terminated is based on the availability of long-term safety and effectiveness data from the OSB Lead-HERo-002 study and published literature.

NCT ID: NCT02191501 Terminated - Obesity Clinical Trials

Endoscopic Suturing of the Gastric Pylorus to Delay Gastric Emptying and Treat Obesity

Start date: May 7, 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to demonstrate the efficacy and safety of endoscopic suturing of the gastric pylorus to delay gastric emptying and treat obesity.

NCT ID: NCT02154984 Terminated - Obesity Clinical Trials

Time Restricted Diet in Obese or Overweight Pre or Postmenopausal Participants

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

The purpose of this study is to study the relationships between obesity, hormones and menopausal status, and breast cancer. The researchers would like to study whether a type of nutritional intervention, called a time-restricted diet or tRD, is easy to maintain using a smartphone application; the researchers also want to study the effect that a tRD has on weight control, hormones, and breast tissue. A tRD is a type of diet that requires people to restrict their daily eating to a specific time frame each day. The researchers think that this might be an effective and manageable way to control weight.