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Pediatric Obesity clinical trials

View clinical trials related to Pediatric Obesity.

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NCT ID: NCT02771951 Completed - Overweight Clinical Trials

Clinical/Behavioral Approach to Overweight in Latino Youth

Luces
Start date: April 2010
Phase: N/A
Study type: Interventional

This randomized controlled trial tests the efficacy of a culturally and linguistically appropriate, evidence-based intervention to slow weight gain or promote weight loss among overweight 6-9 year old Mexican-American children.

NCT ID: NCT02767440 Completed - Obesity Clinical Trials

Families on Track: A Digital Health Behavioral Intervention for Parents Seeking Treatment for Their Child With Obesity

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

Current models of outpatient childhood obesity treatment focus on the child's health habits, with limited efficacy. In part, this may be because childhood obesity is highly sensitive to parental lifestyle habits, who are often not a direct target of child obesity interventions. This study aims to target weight loss among overweight parents of 2-16 year old children with obesity enrolled in the Duke Healthy Lifestyles Program (HL) in order to augment child body mass index reduction. The intervention, " Families on Track" is a digital health intervention platform using the Interactive Obesity Treatment Approach (iOTA).

NCT ID: NCT02759523 Completed - Pediatric Obesity Clinical Trials

Neural Mechanisms Underlying Children's Responses to Food Portion Size and Energy Density

Start date: July 2013
Phase:
Study type: Observational

Increased portion sizes of foods high in energy density (calories per gram of food) have been implicated in the obesity epidemic. Numerous studies show that children and adults eat more from larger portions of food than they do from smaller portions, a response known as the portion size effect. Despite the robust and consistent nature of these findings, the mechanisms underlying the portion size effect are not known. The long-term goal of this research is to identify the neural mechanisms involved in the portion size effect so that this information can be used to develop effective weight-management strategies. Differences in neural response to food cues, as demonstrated by functional magnetic resonance imaging (fMRI), can help clarify the factors that determine susceptibility to large portions. The goal of this study is to identify brain regions activated in response to portion size and energy density and relate these neural responses to laboratory eating behaviors in children. The investigators hypothesize that high relative to low energy density food images will be associated with increased activation in regions of the brain involved in reward- and sensory- processing and that large relative to small portion size food images will be associated with increased activation in regions of the brain involved in cognitive control. In addition, the investigators hypothesize that these brain responses will influence the relationship between portion size served and energy intake at laboratory meals.

NCT ID: NCT02751814 Completed - Childhood Obesity Clinical Trials

Physical Activity and Screen-Time Regulations in Childcare Centers - Aim 2

Pause and Play
Start date: April 2016
Phase:
Study type: Observational

Objective is to examine the physical activity and screen-time behaviors of children enrolled in licensed childcare centers before and after the enactment of new state regulations.

NCT ID: NCT02751788 Completed - Childhood Obesity Clinical Trials

Physical Activity and Screen-Time Regulations in Childcare Centers - Aim 1

Pause and Play
Start date: April 2016
Phase:
Study type: Observational

The goal of this project is to examine the physical activity and screen-time environment of licensed childcare centers before and after the enactment of new state regulations.

NCT ID: NCT02751775 Completed - Childhood Obesity Clinical Trials

Physical Activity and Screen-Time Regulations in Childcare Centers - Aim 3

Pause and Play
Start date: June 2016
Phase:
Study type: Observational

The objective is to establish community priorities for strategies to improve young children's health behaviors based on focus groups of stakeholders in the greater Baton Rouge area.

NCT ID: NCT02741908 Completed - Pediatric Obesity Clinical Trials

Fixed Diet Plan and Calorie Counting Diet in Adolescents

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

Obesity is a chronic illness and multifactorial etiology, related to genetic factors, environmental and behavioral. Features association with several metabolic abnormalities in childhood, leading to increased risk of cardiovascular disease in adult life. The treatment involves lifestyle change, with balanced diet guidance and encouraging physical activity. The treatment in this age group have brought limited data, in addition to high drop-out rates. A unique type of food guidance is the equivalent calorie count, where calories are converted into points. The objective of this study was to evaluate the variance of Z score of body mass index (ZIMC) of obese adolescents undergoing orientation of two groups of low-calorie diet: traditional and based on the points system, as well as evaluate anthropometric variables, body composition, food intake, metabolic changes and self-monitoring. METHODS: randomized clinical study with duration of 24 weeks, with 66 adolescents with an average age of 13.7 ± 0.7 years of both genders, with scores of BMI >= 2 to <= 4 curve adjusted for gender and age of the World Health Organization. Were verified weight, height, blood pressure and waist circumference, intensity of physical activity and self- monitoring, as well as performed the nutritional guidance to each visit. Laboratory parameters, applying the scale of binge eating, pubertal, stage and body composition were evaluated at the beginning and end of the action. The patients were divided into two groups: one that received guidance of traditional low-calorie diet and meet the food consumption record (RCA), three days (Group A) and another that received low-calorie diet guidance based on the system of points and meet the daily RCA (Group B).

NCT ID: NCT02740660 Completed - Pediatric Obesity Clinical Trials

Body Composition Changes With Albuterol and Caffeine Versus Placebo in Adolescents

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

The purpose of this study is to determine whether taking a combination of caffeine and albuterol three times per day will increase muscle and decrease fat in your child's body and to determine how these medications make your child feel. Albuterol is approved by the FDA for the treatment of asthma. It is not approved to increase muscle and decrease body fat in children.

NCT ID: NCT02726529 Completed - Childhood Obesity Clinical Trials

Brighter Bites - Access, Continuity and Education With Fruits and Vegetables

Brighter Bites
Start date: August 2013
Phase: N/A
Study type: Interventional

The purpose of the research is to find out how well a new nutrition program works for elementary school students and their families. This program is called Brighter Bites. Brighter Bites is a school-based program that teaches students and their parents about the importance of eating fresh fruits and vegetables and how to prepare them in tasty, healthy ways. This project is being carried out at six elementary schools in Houston, Texas. Up to 600 first grade students and their parents/guardians are expected to join this project.

NCT ID: NCT02721602 Completed - Type 2 Diabetes Clinical Trials

Families Preventing Diabetes Together

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

The current study proposes to study the feasibility and acceptability of the Families Preventing Diabetes Together Intervention among 40 families who have one parent diagnosed with type 2 diabetes and at least 1 child between the ages of 5-14 years of age. Successful recruitment, measurement and randomization of patients and their families will provide data for our aim of assessing feasibility. Patient and family participation in the intervention and feedback via the post-intervention surveys will provide data for our aim of acceptability.