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Overweight clinical trials

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NCT ID: NCT01320189 Completed - Obesity Clinical Trials

Dietary Protein Requirements on Unbalanced Diets

Start date: May 2011
Phase: N/A
Study type: Interventional

The objective of this study is to determine ad libitum daily energy and protein intake, energy balance and appetite profile in response to protein/carbohydrate and fat ratio over 12 consecutive days, also as a function of age, gender, BMI and FTO polymorphisms.

NCT ID: NCT01317524 Completed - Inflammation Clinical Trials

The Effects of Homogenized and Unhomogenized Milk on Postprandial Metabolism in Healthy Overweight Men

Start date: February 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effects of homogenized, unhomogenized and skimmed milk on postprandial metabolism in healthy overweight men

NCT ID: NCT01317290 Completed - Overweight Clinical Trials

Supplementation of Alpha-linolenic Acid (ALA)-Rich Oil in Humans

ALA_KK
Start date: February 2012
Phase: Phase 0
Study type: Interventional

The objective of this study is to investigate the accumulation of n-3 LC-PUFA (EPA, DPA and DHA) in human lipids by oral supplementation of ALA-rich linseed oil. In addition, the accumulation of n-3 LC-PUFA is compared between subpopulations of different age, gender and physiological conditions (overweight, increased serum total cholesterol).

NCT ID: NCT01316653 Completed - Clinical trials for Overweight and Obesity

Growing Right Onto Wellness (GROW): Changing Early Childhood Body Mass Index (BMI) Trajectories

GROW
Start date: June 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to conduct a randomized controlled trial that examines how a family based, community centered intervention effects early childhood BMI trajectories.

NCT ID: NCT01312051 Completed - Healthy Clinical Trials

Childhood Metabolic Markers of Adult Morbidity in Blacks

Start date: July 2004
Phase: N/A
Study type: Observational

Blacks are at increased risk for obesity, type 2 diabetes mellitus and cardiovascular disease. A common pathogenetic link among these entities is insulin resistance/hyperinsulinemia. The specific aims of this project are: 1) to compare skeletal muscle lipid content (SMLC) in black vs white children by computed tomography (CT) scan of the mid-thigh, and assess the relationship to in vivo insulin sensitivity; 2) to test the hypothesis that free fatty acid (FFA) - induced insulin resistance is associated with larger increases in intramyocellular lipid (IMCL) in black vs white adolescents; 3) to examine if β-cell insulin secretion in prepubertal black children is more sensitive to the stimulatory effect of FFA than in whites; and 4) to test if the β-cell in black obese adolescents is more susceptible to the lipotoxic effect of FFA compared with whites. The methods to be used are: the well- established CT method as well as Magnetic Resonance Spectroscopy (1H-MRS) to assess SMLC and IMCL; intralipid infusion to elevate circulating FFA levels; the hyperinsulinemic-euglycemic clamp with stable isotopes and indirect calorimetry to measure insulin sensitivity and substrate turnover; the hyperglycemic clamp to assess insulin secretion; DEXA and whole body MRI for body composition assessments.

NCT ID: NCT01307644 Completed - Clinical trials for Overweight and Obesity

Web-Based Weight Loss & Weight Maintenance Intervention for Older Rural Women, Also Known as Women Weigh-in for Wellness

Start date: May 1, 2011
Phase: N/A
Study type: Interventional

This project will evaluate an Internet delivery strategy to address weight loss and maintenance among rural midlife and older women.

NCT ID: NCT01306422 Completed - Overweight Clinical Trials

Safety, Tolerability, Kinetics and Efficacy Study of Hoodia Gordonii Purified Extract (PYM50717)

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

The objective of this clinical study was to assess the safety, tolerability, efficacy (effects on appetite scores, food intake) and plasma kinetics of Hoodia gordonii purified extract (H.g.PE), when consumed twice-daily for 2 or 15-days.

NCT ID: NCT01304615 Completed - Overweight Clinical Trials

Foundations for Health

FFH
Start date: February 2011
Phase: N/A
Study type: Interventional

Foundations for Health is a 12-week behavioral weight loss interventions primarily conducted via the internet aimed at helping overweight and obese young adults (ages 18-30) lose weight by increasing physical activity, decreasing the energy density of the diet, and increasing consumption of low energy dense self-made meals by providing culinary training skills.

NCT ID: NCT01299311 Completed - Overweight Clinical Trials

NEAT and Insulin Sensitivity

Start date: December 2010
Phase: N/A
Study type: Interventional

The effect of Non-Exercise Activity Thermogenesis (NEAT) or inactivity on insulin sensitivity and lipid metabolism is unclear. Research recently published shows that activities associated with everyday activities, summarized as NEAT, such as walking and standing, have a much greater role in energy expenditure than exercise. Therefore, the objective of the present study is to evaluate the effect of 4 days of inactivity (mainly sitting), 4 days of everyday activities (sitting, walking and standing), and 4 days of inactivity and exercise (sitting and biking) on glucose metabolism and insulin sensitivity using an oral glucose tolerance test, and on lipid metabolism in sedentary, overweight people. The investigators hypothesize that: 1. 4 days of everyday activities (NEAT) will cause an increased glucose tolerance and increased insulin sensitivity compared to 4 days of inactivity in sedentary, overweight people. 2. 4 days of exercise will improve glucose tolerance and insulin sensitivity more than 4 days of NEAT with equal energy expenditure, in sedentary, overweight people. 3. Fasting triglyceride will have the same course as glucose, mentioned in 1. and 2.

NCT ID: NCT01299051 Completed - Overweight Clinical Trials

Steps to Health: Targeting Obesity in the Health Care Workplace

Start date: January 2011
Phase: N/A
Study type: Interventional

The proposal of this study is to compare the effectiveness of two worksite weight management programs at Duke: Steps to Health (STH) ('usual standard of care') and the more extensive Steps to Health Plus! (STH+). We have added an additional follow-up, by invitation only, for participants in the study who agreed to be contacted for future research.