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Overweight clinical trials

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NCT ID: NCT02413385 Completed - Overweight Clinical Trials

Evidence-Based Lifestyle Prescription Program: Pilot Study

HeSP
Start date: May 2015
Phase: N/A
Study type: Interventional

The HealtheSteps™ (HeS) Program is an evidence-based, community-focused, lifestyle prescription (Rx) program, supported by in-person coaching and innovative health technologies. The program improves the health of Canadians and reduces their risk for chronic disease by tackling three major risk factors that are shared across a number of chronic diseases: physical inactivity, sedentary behaviour and poor diet. Each HeS participant receives an individualized healthy living Rx for exercise, physical activity (step counts) and healthy eating, supported by coaching and technology tools to promote long-term health behaviour change. For this study, the investigators will undertake a 6-month pilot pragmatic randomized controlled trial (RCT), conducted within 5 clinic settings in Southwestern Ontario. The primary aim is to conduct an outcome evaluation to determine the effectiveness of the HeS program in helping at-risk individuals increase physical activity levels, improve eating habits, and improve other health behaviours and health indicators.

NCT ID: NCT02412774 Completed - Type 2 Diabetes Clinical Trials

Effects of Replacing Diet Beverages With Water on Weight Loss and Plasma Glucose Control in Type 2 Diabetes

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

The purpose of the present study is to evaluate the effect of replacing diet beverages with water on weight loss and biochemical indicators for insulin sensitivity and cardiometabolic risk factors of diabetic obese and overweight female adults when they are in a multidisciplinary weight loss plan.

NCT ID: NCT02411825 Completed - Clinical trials for Type 2 Diabetes Mellitus

Multiple Ascending Dose Study in Healthy Male Subjects and Overweight to Obese Male and Female Type 2 Diabetes Mellitus (T2DM) Patients

Start date: March 2015
Phase: Phase 1
Study type: Interventional

Primary Objective: To assess in healthy adult male subjects: - The tolerability and safety of 21-day repeated subcutaneous (SC) doses of SAR425899 including two up titration steps. - Pharmacokinetic (PK) parameters of SAR425899 after ascending repeated SC doses in plasma. - Pharmacodynamic (PD) effects on fasting and postprandial plasma glucose, insulin, biomarkers of lipid metabolism and fibroblast growth factor 21 (FGF21). To assess in overweight to obese T2DM mellitus patients: - The tolerability and safety after 28-day repeated SC doses of SAR425899 including 2 up titration steps. - PK parameters of SAR425899 after ascending repeated SC doses in plasma and urine. - PD effects on fasting and postprandial plasma glucose, insulin, C-peptide, incretin panel (total and active ghrelin, total peptide YY [PYY], total and active glucagon-like peptide -1 [GLP-1], glucagon and total gastric inhibitory polypeptide-1 [GIP]), body weight, FGF21, biomarkers of lipid metabolism and HbA1c.

NCT ID: NCT02410785 Completed - Clinical trials for Overweight and Obesity

Efficacy of Polyglucosamine for Weight Loss

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

The polyglucosamine, specification L112 is a medical device and in this clinical trial used for weight reduction of overweight and obese participants. The rationale for this study is to show that overweight can be reduced by taking 2 times daily 2 tablets with the main meals with the highest fat content.

NCT ID: NCT02410668 Completed - Clinical trials for Overweight and Obesity

The Effects of Flaxseed Supplement on Weight and Biochemical Factors in Overweight and Obese Subject

Start date: March 2014
Phase: Phase 2/Phase 3
Study type: Interventional

To study the effects of Flaxseed supplement on weight, lipid profile and inflammatory factors in subjects with over weight and obesity, 50 patients will be randomly allocated to receive placebo or 30 grams milled Flaxseed for 12 weeks; both groups will be advised to adherence the investigators' diet and exercise program too. At the first and the end of the intervention, weight, waist and hip circumference, lipid profile and some inflammatory markers will be assessed and compared between groups.

NCT ID: NCT02400203 Completed - Overweight Clinical Trials

FREE Living Hulled HEMP Seed and Oil Trial

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

The objectives of this trial are to assess the effects of hemp product consumption, specifically hulled hemp seeds and hemp oil on blood fatty acid profiles and cardiovascular disease risk factors, in healthy overweight volunteers after 4 weeks of consumption.

NCT ID: NCT02399280 Completed - Obesity Clinical Trials

Effect of High Caloric Intake at Lunch Against Dinner on Weight Loss

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

The purpose of the present study is to evaluate the effect of consuming higher caloric intake at lunch in contrast to dinner on weight loss of obese and overweight female adults when they are in a multidisciplinary weight loss plan .

NCT ID: NCT02398253 Completed - Obesity Clinical Trials

Effects of Cognitive Behavioral Therapy (CBT) on Weight Maintenance After Successful Weight Loss

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

The purpose of this study is to assess the effects of CBT after a successful weight loss by a comprehensive weight loss plan on weight maintenance in obese female adults.

NCT ID: NCT02396784 Active, not recruiting - Obesity Clinical Trials

Early Stockholm Obesity Prevention Program (EarlySTOPP-China)

EarlySTOPP-CN
Start date: January 2011
Phase: N/A
Study type: Observational

Early STOPP project promotes good health in children from early age by supporting good habits for the whole family. Our aim is to see if we can prevent overweight and obesity in children in families where parents are overweight or obese. Normal weight parents will also be needed in this study. Background: Several daily habits lead to less favorable health factors. For example, using the car instead of cycling or walking - leads to less activity in everyday life. Individuals also eat more unhealthy foods in larger portions. In combination with genetics, social in heritage and surrounding factors this contributes to increase overweight and obesity among children not only in adults but also in children. Good treatment for childhood obesity are lacking, making prevention very important. The earlier good habits are introduced to a child the better it is. In Early STOPP project we study food, physical activity and sleep habits in the families with a child of one year of age. The height, weight, waist circumference and blood pressure will be recorded in both child and parents. The parents will answer questionnaires about food, physical activity and sleeping habits for both the child and themselves. During the study, the child's physical activity will be measured. Based on our observations we aim to develop the preventive strategies for the families with very young children.

NCT ID: NCT02396524 Completed - Obesity Clinical Trials

Hockey Fans in Training (Hockey FIT): A Pilot Pragmatic Randomized Controlled Trial

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

The Hockey Fans in Training (Hockey FIT) program aims to improve overweight men's physical fitness, eating habits and health-related lifestyle choices through a lifestyle modification program in collaboration with two Ontario Hockey League teams. In this pilot pragmatic randomized controlled trial, the investigators plan to explore the potential for Hockey FIT to reduce a clinically important amount of weight, increase physical activity levels, and lead to improvements in other health-related outcomes.