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Obesity clinical trials

View clinical trials related to Obesity.

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NCT ID: NCT03976089 Completed - Obesity Clinical Trials

Promoting Healthy Development With the Recipe 4 Success Intervention

Start date: April 5, 2013
Phase: N/A
Study type: Interventional

10-session home visit intervention conducted within Early Head Start and designed to reduce low-income toddler's obesity risk and improve their self-regulation skills and parents' sensitivity.

NCT ID: NCT03975556 Completed - Obesity Clinical Trials

Culturally-Adapted Diet for Puerto Rican Adults

Start date: July 1, 2019
Phase: N/A
Study type: Interventional

This pilot project will determine whether a diet culturally-adapted to Puerto Ricans can effectively decrease cardiometabolic risk for diabetes. This will help define a culturally-appropriate, feasible, and sustainable diet intervention aimed at reducing type 2 diabetes and obesity outcomes.

NCT ID: NCT03973424 Completed - Obesity Clinical Trials

Mobile Methods for Reducing Obesity Risk in Parents and Children

PATH
Start date: August 14, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to test the efficacy of an innovative 6-month smartphone-delivered intervention using simplified monitoring of dietary intake compared to a smartphone-delivered intervention with standard calorie monitoring among parents with overweight or obesity.

NCT ID: NCT03968757 Completed - Obesity Clinical Trials

Assessing the Safety and Performance of the easyEndoTM Universal Linear Cutting Stapler in Laparoscopic Gastric Bypass Surgery

Start date: July 4, 2019
Phase:
Study type: Observational [Patient Registry]

The purpose of this observational registry is to evaluate the safety and performance of the easyEndoTM Universal Linear Cutting Stapler and reloads from Ezisurg Medical used in laparoscopic RYGB surgery to create anastomoses. The goal of the study will be achieved by assessing the device performance and reporting of peri- and postoperative complications in a prospectively maintained database.

NCT ID: NCT03968003 Completed - Obesity Clinical Trials

Impact of Dietary Fiber as Prebiotics on Intestinal Microbiota in Obese Thai Children

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

This study evaluates the changes of gut microbiota composition and diversity, body weight, body fat, SCFAs, plasma amino acids, satiety hormones (Peptide-YY(PYY) and glucagon-like peptide(GLP-1)), Inflammatory cytokines (Interleukin-1β(IL-1β), Tumor necrosis factor-α (TNF-α) and Interleukin-6(IL-6)) after 6-month studied period in obese Thai children.165 participants Children, age 7 to 15 years with Body mass index (BMI) ≥ median + 2 standard deviation(SD) will be randomized into one of the three arms of 55 participants per group.Group A (intervention group) will receive inulin 10 g.Group B will receive placebo of isocaloric maltodextrin. Group C will receive dietary fiber advice aimed to match the recommended fiber intake for age.

NCT ID: NCT03967860 Completed - Obesity Clinical Trials

Role of Post Surgery CT Following Laparoscopic Vertical Sleeve Gastrectomy

LSG-CT
Start date: March 6, 2019
Phase:
Study type: Observational

Obesity is a extremely widespread condition in Europe and North America, burdened by a series of complications characterized by major morbidity and morbility. In recent years, bariatric surgery has progressively assumed a leading role in the treatment of morbid obesity and restrictive bariatric surgery procedures, such as laparoscopic vertical sleeve gastrectomy are common. The aim of the study is to retrospectively determine the value of postoperative CT after LSG as an early tool to identify risk factors for the subsequent development of gastric fistula and enable to stratify postoperative risk in asymptomatic patients and ensure effective management of these risk factors.

NCT ID: NCT03967782 Completed - Pediatric obésity Clinical Trials

Effect of the Exercise-meal Timing on Energy Intake and Appetite in Adolescents With Obesity

TIMEX2
Start date: August 31, 2019
Phase: N/A
Study type: Interventional

The aim of the present study is to compare the effect of realizing an exercise right before or right after a meal of on energy intake, appetite feelings and food reward in adolescents with obesity.

NCT ID: NCT03967691 Completed - Healthy Clinical Trials

IL-6 Regulation of Substrate Metabolism and Influence of Obesity

Start date: June 12, 2019
Phase: N/A
Study type: Interventional

The aim of the study is to investigate the effects of blocking IL-6 signaling with tocilizumab on lipid, glucose and protein metabolism during rest and exercise in healthy and obese humans. Interleukin-6 is a molecule produced by a variety of cells and impacts on energy metabolism during fasting and fed conditions. Systemic IL-6 levels are low but increase acutely in response to fasting, exercise and infection, and also chronically in response to obesity and other conditions of lowgrade inflammation.Our recent human intervention study showed that IL-6 receptor blockade prevents exercise training from reducing visceral fat mass. Whether IL-6 receptor blockade directly regulates lipolysis and/or lipid oxidation in humans is however unclear. Therefore, this study will be performed to investigate the physiological role of IL-6 on lipid, glucose and protein metabolism in humans.

NCT ID: NCT03966846 Completed - Obesity Clinical Trials

Kefir and Metabolic Syndrome

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

Metabolic syndrome is a cluster of metabolic disorders which increases the risk for diabetes and cardiovascular disease. In recent years, research has shown that probiotics may have positive effects on metabolic syndrome components. Although several health-promoting effects of kefir, have been suggested, there is limited evidence for its potential effect on metabolic syndrome. Therefore, it is necessary to clarify the effects of kefir on metabolic disorders including obesity, dyslipidemia, diabetes, and hypertension. To address the research gap, this study aimed to investigate the effects of daily kefir consumption on metabolic syndrome components, inflammatory response and gut microbiota composition in adults with MetS. The study was planned as a randomized, controlled, parallel design and completed with a total of 62 individuals who were diagnosed with metabolic syndrome according to the International Diabetes Federation (IDF) criteria. Participants were randomized into two groups and received daily 180 ml of kefir (n=31) or milk (as control) (n=31) for 12 weeks. Participants were assessed at baseline, week 4, week 8, and week 12 and at all controls dietary records, anthropometric measurements, and blood samples were collected. At baseline and 12th-week fecal samples were also collected in order to analyze gut microbiota composition.

NCT ID: NCT03966755 Completed - Obesity Clinical Trials

Unsaturated Fatty Acids to Improve Cardiorespiratory Fitness in Obesity and HFpEF

UFA-Preserved2
Start date: July 23, 2019
Phase: N/A
Study type: Interventional

This study is designed to evaluate the effects of a diet rich in unsaturated fatty acids (UFA)-also known as 'healthy fats'-in patients with obesity and heart failure with preserved ejection fraction (HFpEF) on dietary consumption of UFA as well as fatty acids plasma levels.