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Overweight clinical trials

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NCT ID: NCT03097237 Completed - Obesity Clinical Trials

High Fiber Rye Foods for Weight and Body Fat Reduction

RyeWeight
Start date: September 2016
Phase: N/A
Study type: Interventional

The overall aim of this study is to investigate whether a diet rich in rye fiber from wholegrain rye, compared to refined wheat, as part of a hypocaloric diet leads to larger weight loss and lower body fat content after 12 weeks of intervention. Furthermore the study will investigate the effect on appetite as a potential underlying mechanism for differences in weight loss and body fat reduction.

NCT ID: NCT03096132 Completed - Obesity Clinical Trials

FRESH-DOSE: Families Responsibility Education Support Health-Dual Options for Sustained Effectiveness

Start date: April 18, 2017
Phase: N/A
Study type: Interventional

The objective of the study is to evaluate whether a less intensive intervention, Guided Self-Help Family Based Treatment (gshFBT), is non-inferior to the more intensive Family Based Treatment (FBT) for childhood obesity on child weight loss over 18-months. Cost-effectiveness of both treatments will also be compared.

NCT ID: NCT03095807 Completed - Obesity Clinical Trials

Investigation of Single Ascending Doses of NNC9204-1706 in Male Subjects Being Overweight or With Obesity

Start date: March 20, 2017
Phase: Phase 1
Study type: Interventional

This trial is conducted in the United States of America (USA). The aim of this trial is to assess the safety and tolerability of single doses of NNC9204-1706 administered subcutaneously in male subjects being overweight or with obesity.

NCT ID: NCT03087318 Completed - Clinical trials for Obstructive Sleep Apnea

Sport as a Treatment in Chronic Diseases and Healthcare Sustainability

S4H
Start date: April 5, 2017
Phase: N/A
Study type: Interventional

Obesity, associated with obstructive sleep apnea (OSA) is often involved in cardiovascular diseases. In our study, we want to promote sport practice to reduce that burden in the first place, and all associated diseases (e.g. cardiovascular diseases) consequently. The aim of this clinical trial is to determine which type of program, conducted in a digital environment associating a mobile application and individual coaching, better improves exercise habits over a 3-month period in overweight or moderate obese OSA patients.

NCT ID: NCT03082807 Completed - Obesity Clinical Trials

Dietary Guide in Active Older Adult Men

Start date: February 25, 2011
Phase: N/A
Study type: Interventional

The present study aimed to determine the effects of negative-calorie diet supplemented with exercise, on weight loss and lipid profile, and to compare its efficiency with low-calorie diet with exercise among elderly adult men with abnormal weight gain.

NCT ID: NCT03082794 Completed - Obesity Clinical Trials

Dietary Effects on Weight Loss and Lipid Profile in Sedentary Men

Start date: February 20, 2011
Phase: N/A
Study type: Interventional

Negative-calorie diet is among the popular dieting guides for weight loss; however, there is still little knowledge about this method. The present study aimed to determine the effects of negative-calorie diet on weight loss and lipid profile, and to compare its efficiency with low-calorie diet in men.

NCT ID: NCT03082781 Completed - Obesity Clinical Trials

Dietary Choice in Active Older Adult Women

Start date: October 10, 2012
Phase: N/A
Study type: Interventional

The present study aimed to determine the effects of negative-calorie diet supplemented with exercise, on weight loss and lipid profile, and to compare its efficiency with low-calorie diet with exercise among elderly adult women with abnormal weight gain.

NCT ID: NCT03076060 Completed - Migraine Clinical Trials

Very Low Calories Ketogenic Diet in Migraine.

Ketomig
Start date: January 1, 2017
Phase: N/A
Study type: Interventional

Ketogenesis is a physiologic phenomenon due to starvation or ketogenic diet (KD), a drastic restricted carbohydrate dietary regimen that induces lipid metabolism and ketone body (KB) synthesis. We followed, in a dietician clinical setting, a group of migraineurs who randomly received a one-month prescription of experimental diet, followed by a one-month of carbohydrate progressive reintroduction, then another one-month of experimental diet, followed by a one-month of carbohydrate progressive reintroduction. Experimental diets are a very-low calorie KD, or an isocaloric non-ketogenic diet. Aim of our study is verify if during ketogenesis migraine improves.

NCT ID: NCT03071718 Completed - Obesity Clinical Trials

Diet-induced Arrangement of the Gut Microbiome for Improvement of Cardiometabolic Health

DINAMIC
Start date: June 2016
Phase: N/A
Study type: Interventional

Mediterranean diet (Med-D) has been recognized as an intangible cultural heritage by UNESCO and was shown to be beneficial for the treatment of obesity, type-2 diabetes and cardiovascular diseases. Individuals with the highest adherence to Med-D (classified according to Sofi et al., 2010) were characterized by increased levels of specific fibre-degrading bacteria, increased faecal levels of short chain fatty acids, and lower urinary concentrations of the atherogenic compound TMAO. However, the interplays between Med-D and microbial populations in the intestine remain unclear. Moreover, a number of clinical conditions like obesity, T2D, and atherosclerosis are associated with dysbiotic microbial ecosystems in the gut, i.e., shifts in the structure and function of the microbiota, but the characteristic features of dysbiotic gut communities and the impact of diet are not very well defined. The present study will evaluate the impact of Med-D on cardiometabolic health in human subjects via modification of intestinal microbial communities and its impact on health outcomes, mainly related to inflammatory, oxidative and hormonal status, in overweight subjects.

NCT ID: NCT03070015 Completed - Clinical trials for Overweight and Obesity

The Effects of a Commercially Available Weight Loss Program on Body Weight in Overweight Men and Women

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

The primary purpose of this study (Part A) is to assess changes in body weight and body circumference parameters that are achievable after 4 weeks on the Nutrisystem program compared to a self-directed diet (i.e. Dietary Approaches to Stop Hypertension or DASH). In Part B, subjects on the Nutrisystem program will be given the option to continue the program for another 8 weeks.