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Overweight clinical trials

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NCT ID: NCT00807560 Completed - Obesity Clinical Trials

Parent-Based Treatment for Pediatric Overweight

PO
Start date: September 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine whether a parent/guardian intervention for adolescent overweight/obesity more effective than a nutritional counseling education curriculum for reducing body mass index z-score (BMI Z-score) and related outcomes.

NCT ID: NCT00806260 Completed - Obesity Clinical Trials

A Study to Evaluate How VI-0521 Affect Psychomotor Performance in Healthy Overweight and Obese Subjects.

Start date: December 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine how VI-0521 affect speed and reaction time on specific tasks that require eye and hand coordination, compared to placebo.

NCT ID: NCT00804765 Completed - Obesity Clinical Trials

Impact of Education During Pregnancy in Overweight Pregnant Women

ETOIG
Start date: September 2008
Phase: N/A
Study type: Interventional

Metabolic environment of the foetus during pregnancy in obese women is altered and the child exposed at an increased risk of obesity. Rapid infancy and childhood weight gain is associated with subsequent obesity. The purpose of the study is to test the efficacy of an educational intervention during pregnancy in obese or overweight women, on the reduction of rapid infancy weight gain in the two first years of life.

NCT ID: NCT00799006 Completed - Overweight Clinical Trials

A Single Dose Study Of PF-04620110 In Overweight And Obese, Otherwise Healthy Volunteers

Start date: November 2008
Phase: Phase 1
Study type: Interventional

PF-04620110 is a novel compound proposed for the treatment of Type 2 diabetes mellitus. The purpose of this study is to characterize the safety, tolerability, pharmacokinetics and pharmacodynamics following a single oral dose.

NCT ID: NCT00792207 Completed - Overweight Clinical Trials

The Role of a Virtual Coach in Improving Adherence to an Activity Program for Overweight Adults

StepUp
Start date: June 2008
Phase: N/A
Study type: Interventional

Hypothesis: Overweight subjects using a Virtual Coach will demonstrate improved adherence to an exercise regime. This study is designed to examine the effect of a computer program called a "Virtual Coach" and find out if it helps people become more active. This program acts as a kind of a personal trainer and will give you feedback. All participants in the study will receive an activity monitor to wear during the study and a website to use to track activity. Half of the participants will also receive the virtual coach software. This software will have to be downloaded onto your computer, and we will ask that you check in with the coach using the software three times a week for 12 weeks. The group you will be placed in will be selected by chance.

NCT ID: NCT00785408 Completed - Obesity Clinical Trials

Study to Examine Safety, Tolerability and Effect on Body Weight of Subcutaneous AC2307 in Obese or Overweight Subjects

Start date: December 2008
Phase: Phase 2
Study type: Interventional

A randomized, double-blind, placebo-controlled, parallel-group, dose-ranging study to examine the safety, tolerability, and effect on body weight of subcutaneous AC2307 in obese or overweight subjects.

NCT ID: NCT00780468 Completed - Obesity Clinical Trials

A Pilot Study to Evaluate a Revised Method of Assessing Food in a Commercial Weight Management Program Format

Start date: October 2008
Phase: N/A
Study type: Interventional

This study will provide data on two systems for assigning point values to food choices in a diet plan. The primary purpose of this study is to compare the effectiveness of the two systems with regard to changes in body weight.

NCT ID: NCT00768417 Completed - Obesity Clinical Trials

Availability of Lipids in Almonds in Healthy Individuals

Start date: April 2006
Phase: N/A
Study type: Observational

Evidence indicates that almond consumption is associated with multiple health benefits. However, nuts are commonly excluded from diets on the basis that their high energy content may induce weight gain. Evidence from numerous studies show that this is not the case, yet the mechanism responsible for the less than predicted effect on weight is unknown. This study aimed to examine the effects of increased mastication on lipid bioavailability and satiety related peptide released in humans. Its purpose is to provide valuable mechanistic data to support the results from previous completed clinical studies.

NCT ID: NCT00767208 Completed - Type 2 Diabetes Clinical Trials

Diabetes and Metabolic Postprandial Responses

Start date: January 2005
Phase: N/A
Study type: Interventional

The aim of this trial was to compare postprandial metabolic response to glucose load in healthy overweight and type 2 diabetic subjects, by using glycemia, insulinemia, lipid profile, nutrient oxidation follow-up. Stable isotopes of glucose were used to assess postprandial total,exogenous and endogenous glucose kinetics.

NCT ID: NCT00759746 Completed - Childhood Obesity Clinical Trials

Childhood Obesity Treatment: A Maintenance Approach

COMPASS
Start date: October 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effect of dose and content of an enhanced weight maintenance treatment on children's ability to maintain weight loss following a standard weight loss treatment.