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Overweight clinical trials

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NCT ID: NCT02747316 Completed - Obesity Clinical Trials

Iron Absorption and Transfer to the Fetus During Pregnancy in Normal Weight and Overweight/Obese Women and the Effects on Infants Iron Status

PIANO
Start date: February 2016
Phase: N/A
Study type: Interventional

Overweight and obesity causes low-grade systemic inflammation, which sharply increases risk for iron deficiency. Studies in our laboratory have shown that this is mainly the result of reduced dietary iron absorption because of increased hepcidin concentrations. During pregnancy, women have a large increase in iron needs because of the expansion of maternal blood volume and fetal needs. Iron deficiency anemia in infancy can impair cognitive development. Whether maternal adiposity impairs absorption and transfer of iron to the fetus, and thereby increases risk of iron deficiency in the mother and the infant is unclear.

NCT ID: NCT02745886 Recruiting - Aging Clinical Trials

Metformin Induces a Dietary Restriction-like State in Human

Start date: April 2016
Phase: Phase 4
Study type: Interventional

The fact that metformin treatment has been associated with reduced risk of cancer and cardiovascular disease raises the possibility of a beneficial role of metformin for other age-related diseases. The actions of metformin resemble the effects of calorie restriction (CR) to some extent, and microarray analyses have shown that metformin induces a gene expression profile that aligns with that of CR in animal. The aim of the study is to investigate whether metformin treatment can induce dietary restriction-like state in human. Sixty overweight subjects will be included in this study, and participants will be divided 3 groups (20 cases in each group)including metformin group (0.85, twice daily), standard diet group, and CR group. All subjects will be treated 6 months. At the end of this study, blood samples and muscle samples will be obtained.

NCT ID: NCT02745795 Active, not recruiting - Obesity Clinical Trials

Efficacy of Motivational Interview in the Treatment of Obesity and Overweight in Adolescents

IMAGINE
Start date: October 2015
Phase: N/A
Study type: Interventional

The objective of the study is to investigate the efficacy of motivational interview intervention with adolescent students at a school environment on the adhesion to a therapeutic plan to loose weight.

NCT ID: NCT02743598 Terminated - Obesity Clinical Trials

Liraglutide for HIV-associated Neurocognitive Disorder

Start date: September 2016
Phase: Phase 4
Study type: Interventional

This study will test the effect of liraglutide on cognitive function in HIV-infected overweight or obese subjects with type 2 diabetes.

NCT ID: NCT02742662 Completed - Obesity Clinical Trials

Smart Technology for Weight Loss and Metabolic Health

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

The study will evaluate whether a technology-based lifestyle intervention program using primarily a smartphone platform is an acceptable and effective way for treating obesity. The goal of the program is to achieve weight loss and enhance the health of overweight or obese subjects by improving their diet and activity via smartphone applications as compared with conventional in-person weight management programs.

NCT ID: NCT02741037 Completed - Obesity Clinical Trials

Unidas Por la Vida: A Healthy Lifestyle Intervention for High-risk Latina Dyads

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

Mexican American women have significantly elevated rates of obesity and type 2 diabetes. The proposed study tests a novel intervention that capitalizes on an existing important family dyad (mothers and their adult daughters) to foster clinically significant and long-lasting health behavior change. If found to effective, this intervention strategy has great potential to address health disparities in this, and other, at-risk populations.

NCT ID: NCT02737293 Terminated - Obesity Clinical Trials

Whole Egg Intake and the Mediterranean Diet

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

This project will evaluate the daily intake of whole eggs in the Mediterranean Diet (Med Diet). Cholesterol levels are normally related to cardiovascular disease (CVD) risk. Dietary fat and the total diet makeup are well known modifiers of CVD risk. The Med Diet has been shown to decrease blood lipids (fats) and reduce inflammation. Cholesterol intake from eggs may not be as bad as once thought and, in fact, may help to improve the blood lipid (fat) levels. This study is being done to test how the addition of eggs to a Med Diet affects blood lipids and other risk markers for CVD.

NCT ID: NCT02736669 Active, not recruiting - Obesity Clinical Trials

CARE Trial: Comparing Different Levels of Calorie Reduction for Weight Loss

CARE
Start date: October 2015
Phase: N/A
Study type: Interventional

This research study will compare two weight loss programs that provide different recommendations for how to reduce your energy (or calorie) intake to achieve weight loss in an effort to determine if fixed calorie reduction or varied calorie reduction is more effective for weight loss.

NCT ID: NCT02731768 Completed - Obesity Clinical Trials

Nutrition, Exercise, and Technology for Weight Loss

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

The purpose of this study is to evaluate whether a social support-enhanced, technology-based, behavioral weight control intervention can improve weight loss over existing best practices.

NCT ID: NCT02721251 Terminated - Overweight Clinical Trials

Influence of Exercise, Weight Loss, and Exercise Plus Weight Loss on Sleep Apnea

Start date: April 1, 2016
Phase: N/A
Study type: Interventional

Obstructive sleep apnea (OSA) is highly prevalent among Veterans, and is associated with significant mortality and multiple morbidities. Available treatments have had limited effectiveness in treating OSA and alleviating associated morbidity. The investigators' previous research found a reduction in OSA severity of approximately 25% following modest exercise training. That this effect occurred independent of weight loss raises the exciting possibility that exercise combined with weight loss could reduce OSA by at least 50% and have unique health benefits for OSA patients. Following screening and baseline assessments, 90 overweight Veterans ages 18-60 years with OSA will be randomized to one of three 16-week treatments: (1) exercise training; (2) 10 % weight loss; and 3) exercise + weight loss. Changes in OSA and related morbidity will be compared between treatments.