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Feeding Behavior clinical trials

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NCT ID: NCT04253938 Recruiting - Feeding Behavior Clinical Trials

Evaluation of Feeding Practices in Latin American Infants at a Medical Home in Austin, Texas

Start date: December 15, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the methods of formula preparation and feeding practices in Latin American households in the first 12 months of life. There is limited published information on the feeding practices of infants in disadvantaged households, and still less information is available regarding disadvantaged Latin American households. Studies have shown that certain feeding practices such as diluting infant formula, warming bottles in a microwave, or storing partially used bottles in the refrigerator can be dangerous for the infant. Previous pilot data in other states have documented that up to 15-21% of parents dilute infant formula. Motives for doing so included an attempt to avoid infant hunger, save money, or make formula last longer.

NCT ID: NCT04208256 Recruiting - Adolescent Clinical Trials

Food Intake and the Adolescent Brain

ADOB
Start date: December 30, 2019
Phase: N/A
Study type: Interventional

The brain plays an integral role in how and what people eat. However, the brain's contribution to overeating is not well understood during sensitive developmental periods such as adolescence, when excessive weight gain and obesity prevalence are a significant concern.The proposed study will use functional magnetic resonance imaging to examine how the brain's response to excess energy is related to overeating in adolescents with and without obesity.

NCT ID: NCT04041505 Terminated - Breastfeeding Clinical Trials

Responsive Feeding of Infants With Expressed Milk

REFINE
Start date: August 15, 2019
Phase: N/A
Study type: Interventional

Nova Scotia has among the lowest breastfeeding rates in Canada, with less than one quarter of infants receiving Health Canada's recommended 6 months of exclusive breastfeeding. Compared with feeding formula, breastfeeding has been linked with a number of health advantages, including fewer infections, higher IQ, and a lowered risk of obesity later in life. How infants consume human milk is changing. Pumping milk has grown in popularity in recent years because some mothers may feel stigmatized breastfeeding, especially in public, but also because it allows other caregivers to help with feeding. Although pumped human milk is considered equal to breastfeeding, there is very little research in this area, especially around responsive feeding and later health outcomes. Since pumped milk is fed from a bottle, the health benefits may be lost (for instance, this may impact a baby's ability to understand if s/he is hungry or full). The primary aim of this study is to determine if the volume of human milk an infant consumes differs if they consume milk from a bottle versus the breast. The investigators will conduct a cross-over trial in which 62 mother-infant pairs will be randomized to feed at the breast or from a bottle for 24 hours, have a 24 hour wash-out period, and then 'cross-over' to another 24 hour session with the opposite 'treatment.' The volume of milk consumed at each feed within the 24 hour window (via indirect weighing, or weighing the baby before and after eating) will be recorded to determine if there are differences in milk consumption. Mother-infant pairs will complete this 3-day study three times, at 6 weeks, 4 months, and 6 months. Information from this study will help to better understand current infant feeding practices in Nova Scotia, and the potential role this plays in future health outcomes. Evidence from this study may help to identify means of improving feeding practices and promoting human milk as the main food for Nova Scotian infants, setting them on a path for the best start in life.

NCT ID: NCT04037306 Terminated - Diet Habit Clinical Trials

Measurements From Stool to Support Dietary Change

Start date: July 30, 2019
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate if daily feedback on food-derived metabolites in stool enhances an individual's ability to make and/or sustain a dietary change.

NCT ID: NCT03992118 Completed - Clinical trials for Autism Spectrum Disorder

Project LEaH: Learning to Eat at Home

Start date: August 7, 2018
Phase: N/A
Study type: Interventional

The investigators are trying to determine if delivery a feeding intervention program using videoconferencing technology is feasible.

NCT ID: NCT03949543 Completed - Feeding Behavior Clinical Trials

The Timing of Main Meal Consumption Effect on Gut Microbiota and Host

TIMC
Start date: October 10, 2017
Phase: N/A
Study type: Interventional

The interplay between diet and the gut microbiota has been implicated in the onset of cardiovascular disease. The gut microbiota displays diurnal rhythms, which may be influenced by meal timing. This study aimed to investigate the effect of main meal consumption timing on the microbiota and the cardiometabolic factors of the host using a cross-over RCT in healthy adults The main outcome measurements will be: a) changes in gut microbiota composition based on 16S rRNA gene amplicon sequencing and shotgun metagenomics, b) changes in bacterial functional capacity) and urinary/faecal metabolomics, c) changes in targeted bacterial metabolites, d)Inflammatory markers The aim of this study is to explore the effect of the timing of main meal consumption on gut microbiota and immune response in healthy adults.

NCT ID: NCT03941392 Completed - Health Behavior Clinical Trials

Nutritional Study in Spanish Pediatric Population

EsNuPI
Start date: October 2, 2018
Phase:
Study type: Observational

This study investigates the aspects related to the intake of food and nutrients, physical activity and sedentary behavior of Spanish children from 1 to 9 years. Furthermore, the investigators will know if the consumption of dairy products is associated with a better dietary pattern. Hypothesis: The habitual consumption of dairy products as part of a regular diet is associated with a better dietary pattern and a higher global diet quality.

NCT ID: NCT03926065 Completed - Feeding Behavior Clinical Trials

Variations in Palatability and Portion Size of Vegetables on Meal Intake of Preschool Children

Start date: May 28, 2019
Phase: N/A
Study type: Interventional

The aim of the study is to determine the effect of varying both the palatability and portion size of vegetables served to preschool children at a meal on the outcomes of food and energy intake at the meal.

NCT ID: NCT03886428 Completed - Feeding Behavior Clinical Trials

The Influence of Satiation Measures on the Portion Size Effect

Start date: May 21, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to gain a better understanding of the satiation measures that influence human eating behavior in regard to intake of large portion sizes at a meal. The investigators hypothesize that satiation measures will influence the magnitude of the portion size effect at a meal. Additionally, other individual characteristics will be examined for their influence on the portion size effect. The portion size effect will be measured by serving a test meal once a week for four weeks in which the portion size of the entree will be varied.

NCT ID: NCT03815019 Recruiting - Feeding Behavior Clinical Trials

iKanEat: A Randomized-controlled, Multi-center Trial of Megestrol for Chronic Oral Food Refusal in Children

iKanEat
Start date: August 15, 2019
Phase: Phase 4
Study type: Interventional

This is a multi-center, randomized, placebo-controlled, double-blind clinical trial. The primary focus of the study is the evaluation of the effectiveness of treatment with megestrol as part of a 24 week behavioral feeding protocol in transitioning from tube to oral feedings in a pediatric population. Approximately 60 pediatric subjects matching the criteria for eligibility will be enrolled in the study and randomized to receive either megestrol (n=30) or placebo (n=30).