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Obesity clinical trials

View clinical trials related to Obesity.

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NCT ID: NCT03024879 Enrolling by invitation - Healthy Clinical Trials

The Effect of Motilin on the Frequency and Amount of Food Intake

Start date: March 2014
Phase: Phase 4
Study type: Interventional

In this study, the investigators aimed at evaluating the role of motilin in the regulation of food intake. Motilin, a gastrointestinal hormone, is a hunger signal in healthy volunteers and is significantly increased in obese patients. Its role in food intake regulation might contribute to the pathogenesis of obesity.

NCT ID: NCT02985307 Enrolling by invitation - Obesity Clinical Trials

Impact of Mobile Phone Texting Service to Support Weight Loss

SMS
Start date: April 28, 2017
Phase: N/A
Study type: Interventional

This study evaluates the efficacy of a mobile telehealth short message service as a facilitator for weight management. Half of the participants will receive a standard care weight management group intervention, while the other half will receive daily text messages via their mobile phone to help facilitate weight loss. It is hypothesized that the intervention group receiving text messages will be as successful as the control group at achieving weight loss over a 3-month period.

NCT ID: NCT02910869 Enrolling by invitation - Obesity Clinical Trials

PREDICT: Nutrigenetic Profile of Patients With Weight Loss Success

PREDICT
Start date: September 2016
Phase: N/A
Study type: Observational

This observational study will investigate the potential clinical utility of the Pathway Fit® test by investigating whether patients who successfully lose weight (defined as losing at least 5% of body weight 8 weeks after initiation) in the MOVE! or TeleMOVE! Weight Management programs have a distinct nutrigenetic profile over those that were unable to lose a significant amount of weight. We will use electronic records to identify all individuals who have successfully completed the MOVE! program (i.e. attended the full 8 week course) or TeleMOVE! program. In addition we will find age- and gender- matched individuals who attended and completed the MOVE! or TeleMOVE! programs but did not lose weight. After completion of the MOVE! or TeleMOVE! programs Veterans will submit a saliva sample for the Pathway Fit® test. Also, blood will be collected for storage for further studies on metabolomics. The start and end weight of all participants will be recorded. The nutrigenic profiles of those with successful weight loss will be compared to those less successful to determine if this cohort has a particular genetic profile.

NCT ID: NCT02790112 Enrolling by invitation - Adiposity Clinical Trials

Long-term Outcome of GnRH Analogues Treatment of Children With Idiopathic Central Precocious Puberty

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

This study evaluates the influence of early adiposity rebound, genetic polymorphisms and GnRHa treatment on long-term outcome of girls with idiopathic central precocious puberty.

NCT ID: NCT02669797 Enrolling by invitation - Childhood Obesity Clinical Trials

Family Matters Intervention

Start date: February 11, 2022
Phase: N/A
Study type: Interventional

The proposed study is a 12-month, individual randomized controlled trial (RCT). The main aim of the study is to decrease childhood obesity (BMI percentile, neck circumference) and improve child diet quality in children ages 5-10 years old by increasing family meal quality (i.e., dietary intake, interpersonal atmosphere) and quantity (i.e., frequency of family meals) via innovative technology (i.e., ecological momentary intervention (EMI), video feedback) and partnerships with primary care and Community Health Workers (CHWs).

NCT ID: NCT02645422 Enrolling by invitation - Childhood Obesity Clinical Trials

Genetic Determinants and Clinical Consequences of Early-onset Severe Obesity

PeLi
Start date: December 2015
Phase:
Study type: Observational

The aim of the present study is to identify new obesity-related genetic defects and determine their association with clinical manifestations in families with childhood-onset severe obesity. The investigators hypothesize that by exploring children with severe early-onset obesity they can find new obesity-related genetic defects and by exploring obesity-associated clinical manifestations the investigators can elucidate the outcomes of severe childhood obesity.

NCT ID: NCT02637388 Enrolling by invitation - Obesity Clinical Trials

Effects of Beta-glucan on Energy Intake and Satiety

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

The purpose of this study is to address the effect of consuming 4g of soluble fibre beta-glucan at breakfast on satiety and food intake.

NCT ID: NCT02532829 Enrolling by invitation - Obesity Clinical Trials

Human Intestinal Peptides Evaluation and Research

HIPER
Start date: September 2015
Phase: N/A
Study type: Observational

The HIPER-1 study is a single centre cross sectional study in which a total of 240 participants (in different metabolic states and surgical models) will receive an Oral Mixed Meal Tolerance Test (OMTT). At baseline and after 30, 60 and 120 minutes the PYY levels, GLP-1 levels, glucose and insulin sensitivity will be measured. The primary endpoint of the study will be the area under the GLP-1 and Peptide - YY curves and insulin sensitivity following the OMTT.

NCT ID: NCT02523352 Enrolling by invitation - Obesity Clinical Trials

Effects of PEEP on Heart and Lungs in Obese Subjects

Start date: April 5, 2018
Phase: N/A
Study type: Interventional

Aim of this study is to better understand pathophysiology of the alteration of respiratory mechanics and cardiovascular function in obese volunteer subjects. The investigators plan to test this hypothesis with a physiological, interventional study conducted on volunteers by using Electrical Impedance Tomography in a group of patients and magnetic resonance imaging (MRI) in another group.

NCT ID: NCT02498990 Enrolling by invitation - Obesity Clinical Trials

Low Calorie Diet and Diabetes

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

The primary hypothesis is to investigate whether a low calorie diet for 7 weeks followed by continuous lifestyle advice is an effective option to achieve an improvement in glucose control as measured by HbA1c after 52 and 104 weeks as compared to baseline values in obese type 2 diabetes patients on either tablet or insulin treatment. The secondary hypothesis is to investigate whether the weight reduction therapy also has significant impact on various anthropometric, clinical and metabolic parameters associated with obesity.