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Overweight clinical trials

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NCT ID: NCT02000037 Terminated - Clinical trials for Assess the Effect of an IR Reflexotherapy on Overweight and Class I Obese People

Interest in the Medium Term of an Infrared Reflexotherapy on Overweight or Class I Obese People

REFLEX-IR
Start date: October 18, 2013
Phase: N/A
Study type: Interventional

The study aim is to Assess the Effect of an IR Reflexotherapy on Overweight and Class I Obese People.

NCT ID: NCT01933633 Terminated - Obesity Clinical Trials

Improved Fertility After Exercise in Overweight/Obese Women

FertilEX
Start date: September 2013
Phase: N/A
Study type: Interventional

Overweight/obesity is associated with sub-fertility. The investigators will assess if regular exercise training prior to assisted fertilization will improve pregnancy rate in overweight/obese women referred to assisted fertilization. It is expected that training will be successful in increasing pregnancy rate

NCT ID: NCT01796340 Terminated - Obesity Clinical Trials

Cue Exposure Training for Overweight Children

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

The primary objective of the study is to investigate the effectiveness of two intensive two-session trainings, the conventional psycho-education and food cue exposure, on eating in the absence of hunger, binge eating and Body Mass Index (BMI) change in overweight/ obese children.

NCT ID: NCT01764425 Terminated - Clinical trials for Healthy, Overweight and/or Obese Subjects

Clinical Trial to Study the Safety Tolerability, Pharmacokinetics, Food Effect & Pharmacodynamics of a New Compound P7435 in Healthy, Overweight and/or Obese Subjects

Start date: May 2012
Phase: Phase 1
Study type: Interventional

Clinical trial to study the safety tolerability, pharmacokinetics, food effect and pharmacodynamics of a new compound P7435 in in healthy, overweight and/or obese subjects

NCT ID: NCT01698606 Terminated - Childhood Obesity Clinical Trials

FOR HEALTH: A Family-oriented Healthy Eating, Activity and Lifestyle Intervention for Overweight Preschool Children

FOR HEALTH
Start date: January 2013
Phase: N/A
Study type: Interventional

In this 3-phase study, following an initial small-scale (phase 1) feasibility trial, the aim of phase 2 of the project is to investigate whether a community-based, 12-month intervention for overweight and obese preschool children 2-6 years of age and their families will be effective in reducing the participants' degree of overweight (BMI z-score) and in improving quality of life. In the final phase (phase 3), participating children will be randomized to either receiving a multidisciplinary lifestyle intervention during the first 6 months (treatment arm), or 6 months later (control or wait list arm), in order to generate more robust effectiveness data. Participants will receive an additional free 6-month YMCA membership while participating in the study.

NCT ID: NCT01644201 Terminated - Obesity Clinical Trials

A Study Evaluating the Effects of a High Viscosity Non-starch Polysaccharide (PolyGlycopleX® - PGX®) on Glycemic Control, Cardiometabolic Risk Factors and Weight Loss in Overweight and Obese Type II Diabetics

Start date: October 2012
Phase: Phase 3
Study type: Interventional

One out of two adults in Canada is currently overweight and therefore at increased risk for a number of medical conditions including diabetes, high blood pressure, heart attacks and stroke. Obesity is less prevalent in populations consuming large amounts of dietary fibre, suggesting that fibre intake could play an important role in prevention and progression of obesity and diabetes and other conditions. Several studies have suggested that fibre has a positive effect on blood sugar and may help lower body weight. The purpose of this study is to help better understand the effect of adding fibre supplementation to a low calorie diet on blood sugar control and weight loss. The investigators hypothesize that blood sugar control will improve in participants in the fibre supplementation group. Men and women, with stable Type 2 Diabetes (e.g. no medication change in the last 3 months), between 18 - 75 years of age, and with a Body Mass Index (BMI) between 27 - 60 kg/m2 can participate in this study.

NCT ID: NCT01634646 Terminated - Overweight Clinical Trials

Observational Study of Lyzme5 Impact on Cholesterol and Body Weight in Man

Lyzme5
Start date: May 2012
Phase: N/A
Study type: Interventional

This observational placebo-controlled pilot study is intended to document whether or not Lyzme5, an over-the-counter (OTC) proprietary nutritional supplement product can positively impact, (a) weight and, (b) cholesterol levels in man.

NCT ID: NCT01601704 Terminated - Obesity Clinical Trials

Cardiovascular Outcomes Study of Naltrexone SR/Bupropion SR in Overweight and Obese Subjects With Cardiovascular Risk Factors (The Light Study)

Start date: June 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the effects of NB relative to placebo on major adverse cardiovascular events (MACE) such as cardiovascular death, non-fatal myocardial infarction, and non-fatal stroke in overweight and obese subjects who are at a higher risk of having these events because they have diabetes and/or other cardiovascular risk factors.

NCT ID: NCT01574573 Terminated - Obesity Clinical Trials

Impact of Weight Loss on Gastroesophageal Reflux Disease in Overweight and Obese Subjects: a Prospective Study

Start date: June 2009
Phase: N/A
Study type: Interventional

By affecting the gastroesophageal pressure gradient, obesity predisposes to reflux of gastric contents. The investigators hypothesized that the loss of weight will decrease this gradient and as a result decrease the severity and frequency of GERD symptoms. GERD negatively affects health related quality of life. Since loss of weight may decrease gastroesophageal reflux, the investigators hypothesized that it obesity contributes to poor quality of life in GERD subjects and losing weight should also favorably impact and improve quality of life in GERD patients.

NCT ID: NCT01540864 Terminated - Obesity Clinical Trials

A Safety and Efficacy Study of HPP404 on Weight Loss in Overweight or Obese Subjects

Start date: May 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare the safety and effect of HPP404 versus placebo on body weight in overweight or obese subjects.