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Feeding Behavior clinical trials

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NCT ID: NCT02996422 Completed - Feeding Behavior Clinical Trials

Appalachians Together Restoring the Eating Environment: Improving Healthy Diet in Rural Appalachian Kentucky

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

Most of the nation's serious chronic health challenges and causes of death, including diabetes, heart disease, cancer, and obesity, are directly linked to sub-optimal diet. Both poor diets and associated disease are disproportionately common in the Appalachian counties of eastern Kentucky, a region with stark health inequities, including elevated rates of obesity, overweight, and premature mortality. The purpose of this study is to evaluate a multi-component intervention developed through community-based participatory research methods for improving access to healthy foods and enhancing dietary intake in eastern Kentucky. The intervention components evaluated in this study consist of: 1) a school-based campaign to promote water consumption in middle and high schools and 2) a series of group cooking classes for adults.

NCT ID: NCT02963987 Completed - Feeding Behavior Clinical Trials

Effect of Portion Size Over 5 Days in Preschool Children

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

In this study, the investigators varied the portion size of all meals served during two 5-day periods. During one period, baseline amounts of all foods and beverages were served, and during the other, the portion size of all items was increased by 50%. The primary aim of the study is to determine the effect of varying the portion size of foods and beverages served over 5 days on energy intake in preschool children.

NCT ID: NCT02962609 Completed - Feeding Behavior Clinical Trials

Effect of Feeding Positions of Preterm Infants on Some Physiological Characteristics

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

The purpose of this study is to determine the effect of Semielevated Side-Lying (ESL) and Semielevated Supine Position (ESU) positions used in bottle-feeding of very preterm infants upon their physiological characteristics and feeding performances.

NCT ID: NCT02930642 Completed - Obesity Clinical Trials

Food Insecurity, Obesity, and Impulsive Food Choice

FIOI
Start date: May 31, 2017
Phase: N/A
Study type: Interventional

The objective of this study is to determine the relations among food insecurity status, obesity, and impulsive food choice patterns and to test the extent to which a mindful eating strategy reduces impulsive choice for food. The central hypothesis is that food-insecure individuals will demonstrate more impulsive food choice patterns and demonstrate a greater likelihood of obesity than individuals who are food secure. Two specific aims are proposed: Specific aim #1: Determine the relation between food insecurity, obesity, and impulsive food choice patterns in women. The working hypothesis is that food-insecure individuals, especially those that are obese, will exhibit more impulsive food choice patterns than food-secure individuals. Specific aim #2: Determine the efficacy of an extended mindfulness-based eating strategy on impulsive choice patterns among food insecure women. The working hypothesis is that mindful eating will reduce impulsive food choice patterns relative to baseline and control conditions, and will persist to follow-up. The investigators expect mindful eating to reduce impulsive choice compared to control conditions, despite food security status.

NCT ID: NCT02696343 Completed - Feeding Behavior Clinical Trials

Somatosensory Modulation of Salivary Gene Expression and Oral Feeding in Preterm Infants

Start date: July 13, 2016
Phase: N/A
Study type: Interventional

Two innovative approaches, pulsatile orocutaneous entrainment of non-nutritive suck via orosensory entrainment (NTrainer) device technology and serial salivary gene expression analyses, will be merged to examine the relation between gene expression, oral somatosensory stimulation, feeding behavior, and neurodevelopmental outcomes at 18 months corrected age (CA) on 180 extremely preterm infants [EPIs] (24 0/7-26 6/7 GA and 27 0/7 - 28 6/7 GA) enrolled at three neonatal intensive care units: Catholic Health Initiative (CHI) Health St. Elizabeth (Lincoln, NE), Tufts Medical Center (Boston, MA), and Santa Clara Valley Medical Center (San Jose, CA). EPIs will be randomized to a blind pacifier (SHAM) or PULSED NTrainer treatment groups, and stratified by GA, sex, and bronchopulmonary dysplasia status (BPD vs non-BPD). We hypothesize that the combination of the NTrainer® intervention for improved oral feeding skills, along with objective salivary gene expression data to monitor response to treatment and feeding development, will result in a novel, objective, and personalized approach to neonatal oral feeding and reduce the duration of time to attain oral feeds while improving feeding, growth and neurodevelopmental outcomes at 18 months' CA.

NCT ID: NCT02689791 Completed - Feeding Behavior Clinical Trials

Effect of Resistant Wheat Starch on Subjective Appetite and Food Intake in Healthy Adults

Start date: January 2012
Phase: N/A
Study type: Interventional

A randomized, single-blind, cross-over study was conducted to determine the effect of replacing standard wheat flour (SWF) with resistant wheat starch (RWS) on markers of appetite and food intake in healthy adults.

NCT ID: NCT02624206 Completed - Feeding Behavior Clinical Trials

Specificity of Flavor-Nutrient Learning: An fMRI Experiment

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

This is an etiology study designed to examine the how people's brains and behaviors respond to regularly consuming a beverage. Participants are assessed at 2 behavioral assessments (Wave 1 and Wave 2), 2 scans (at the BRIC), and at 9 'intervention' assessments (5-10mins) different time periods throughout the study. At their first assessment (W1) they are randomized into one of two juices.

NCT ID: NCT02484846 Completed - Sleep Deprivation Clinical Trials

Impaired Vigilance, and Its Effects on Cognition and Behavior

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

Fifty healthy, young participants (10 male, 40 female) completed two 3-hour study sessions that were at least five days apart. The first session was a baseline. The sleep intervention took place on the night prior to Session 2, where the amount of time in bed was manipulated to be 60-130% of the individual's habitual sleep time. Within both sessions, subjective (Stanford Sleepiness Scale, SSS) and objective (Psychomotor Vigilance Test, PVT) alertness were measured. During the middle of each session, a 40-minute ad libitum meal opportunity allowed participants to eat from eight different food items. Food healthfulness, caloric density, distribution and number of calories were measured and compared to alertness levels.

NCT ID: NCT02438878 Completed - Breastfeeding Clinical Trials

Supporting Baby Behavior Through Pediatric Offices

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

The primary objective of this project is to evaluate the impact on infant growth and infant-feeding practices of a low-cost series of video trainings and tools targeted to medical staff and designed to support ongoing Baby Behavior education of WIC participants.

NCT ID: NCT02347527 Completed - Obesity Clinical Trials

Neuronal and Behavioral Effects of Implicit Priming in Obese Individuals

Start date: May 2013
Phase: N/A
Study type: Interventional

The overall goals of this project are to determine the impact of an implicit priming intervention, designed to alter food perceptions, on both brain responses to food and on food intake behaviors in overweight/obese individuals. The investigators hypothesized that this bottom-up sensory-level conditioning approach would effectively result in reduced preference for high-calorie foods.