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Overweight clinical trials

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NCT ID: NCT02930681 Completed - Clinical trials for Hyperglycemia, Postprandial

Efficacy of Glucosanol™ in Reducing Post-prandial Glucose Levels in Overweight Subjects

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

Glucosanol had previously been proven to be effective in aiding weight loss and weight loss maintenance. Studies have also shown that Glucosanol (also known as Phaseolamin), was effective in aiding weight loss and also has evidence on reducing post-prandial glucose levels. This study is to enrich the existing evidence on dose-dependent post-prandial glucose effects of Glucosanol

NCT ID: NCT02930668 Completed - Clinical trials for Overweight and Obesity

Efficacy and Safety of Glucosanol™ in Body Weight Reduction

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

It was proven in a previous clinical study that Glucosanol™ is effective and safe in reducing weight in the overweight and obese. The present study aims at expanding the data concerning the weight management effect of Glucosanol™ in overweight and moderately obese population.

NCT ID: NCT02925572 Recruiting - Clinical trials for Adolescents (12 to 17 Years Old)

Teenagers: Impact of Eccentric eXercise Training on Overweight and Obesity

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

Nowadays, eccentric exercise can be realized in a dynamic way with an ergocycle which permits eccentric (ECC) lower limbs contractions at a defined power output. With this type of ergometer, O2 consumption (VO2) in ECC is three fold lower than in concentric (CON) for the same power output. Consequently, ECC program could be used in chronic disorders with limited capacities, such as obesity. The investigators hypothesis that an eccentric training program, as it will induce higher mechanical constraints, would improve body composition, especially by reducing fat mass. This effect could be explained by an increased rest energy expenditure and a better improvement in biological parameters (particularly lipid profile and insulin-resistance) after ECC training (versus CON training). This study aims to compare the modification of fat mass after an ECC program versus a CON program at the same VO2.. The secondary goal is to assess the physiological mechanisms involved in the modification of body composition.

NCT ID: NCT02924025 Completed - Clinical trials for Overweight and Obesity

Motivational Interviewing as an Intervention for PCOS

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

The aim of the study is to examine if motivational interviewing can have a positive effect on weight loss over a 6 month period. By losing weight, the investigators assume the patients will have a positive effect on quality of life, and also that weight loss will help to regulate the factors that are present with polycystic ovary syndrom (PCOS); such as menstrual disorders and infertility. Participants will be randomly assigned to a treatment group and a control group. Both groups will be followed as normal with blood samples and other tests such as scans of the ovaries and measurement of height and weight at the beginning of the study and after six months. In addition, there will be a small hair sample taken from the neck at the first consultation and after 6 months. This is done to measure the stress hormone cortisol in the body over the duration of the experiment. The treatment group receive individual motivational interviews by a nurse every 14 days for a period of six months. After half a year, tests are repeated to see if there are significant differences between the groups.

NCT ID: NCT02920190 Withdrawn - Obesity Clinical Trials

Antigen-Lipid-Driven Monoclonal Gammopathies Targeting Epicardial Fat

Start date: September 1, 2020
Phase: Phase 4
Study type: Interventional

The purpose of this research study is to learn about the effect of Liraglutide (Victoza) on the fat of the heart and some fat cells in blood.

NCT ID: NCT02915913 Completed - Obesity Clinical Trials

Effects of Exercise Training on Cognitive Function and Neurotrophic Factors in Overweight Adults

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

The BrainFit Study aims to examine acute effects of High Intensity Interval- vs Resistance or Combined program has benefits on Cognitive Function as well as on secretion and regulation of neurotrophic factors or neurotrophins in a cohort of sedentary, overweight adults (aged 18-30 years) from Bogota, Colombia.

NCT ID: NCT02910817 Completed - Clinical trials for Polycystic Ovary Syndrome

Impact of Metformin on In Vitro Fertilization Outcomes in Overweight and Obese PCOS Women

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

RCT to investigate whether metformin co-treatment would improve IVF outcomes in overweight and obese women with PCOS.

NCT ID: NCT02910648 Completed - Clinical trials for Overweight/Obese Population

Healthy Behaviors Learning Task and Sleep

NAP
Start date: July 2016
Phase: N/A
Study type: Interventional

This research is being done to study the impacts of a computerized learning task on health behaviors. The investigators are interested in studying whether this computerized learning task can help with weight loss.

NCT ID: NCT02910544 Completed - Clinical trials for Osteoarthritis, Knee

Weight Loss and Physical Activity in Overweight/Obese Individuals With Knee Osteoarthritis

Start date: November 2016
Phase:
Study type: Observational

This is a substudy to a randomised trial investigating the effect of liraglutide on body weight and pain in overweight or obese patients with knee osteoarthritis (NCT02905864). In the parent trial, patients will be subjected to an 8-week diet intervention phase including a low-calorie diet and dietetic counselling, after which.they will be randomised to receive either liraglutide 3 mg or liraglutide 3 mg placebo as an add-on to dietetic guidance on re-introducing regular foods and a focus on continued motivation to engage in a healthy lifestyle. This substudy aims to investigate any changes in physical activity associated with the initial 8-week weight loss intervention.

NCT ID: NCT02905422 Active, not recruiting - Overweight Clinical Trials

Healthy Eating, Activity, & Lifestyle Training Headquarters: II Pilot Project

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

The proposed study aims to combine evidenced based tools and guidance (H.E.A.L.T.H.: Healthy Eating Activity Lifestyle Training Headquarters) previously tested that has been developed specifically for use by Army Soldiers and a remote clinical intervention model that includes mobile tracking technology/devices for physical activity, weight and nutrition. This program is called the H.E.A.L.T.H. Intensive.