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Meals clinical trials

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NCT ID: NCT05852548 Completed - Clinical trials for Autism Spectrum Disorder

Parent-Mediated Intervention for Families With Children With Autism and Feeding Challenges, Australia Cohort

Start date: June 24, 2023
Phase: N/A
Study type: Interventional

The goal is to expand a parent-mediated intervention for feeding challenges in children with autism with an Australian cohort, building on recent research and current successful models already being used. A parent-mediated intervention would primarily occur in the home environment, working with the parent to establish goals and implement the intervention based on their child's specific needs.

NCT ID: NCT03252704 Completed - Glucose, High Blood Clinical Trials

Post-prandial Glycemic Response to Fiber in Healthy Adults

Start date: March 31, 2016
Phase: N/A
Study type: Interventional

This randomized, double-blind, comparator controlled trial evaluated the blood glucose and insulin responses in healthy adults, after consuming a high fiber or low fiber muffin top.

NCT ID: NCT03071120 Completed - Clinical trials for Autism Spectrum Disorder

Parent-Mediated Intervention for Families With Children With Autism and Feeding Challenges

Start date: February 3, 2017
Phase: N/A
Study type: Interventional

The goal is to pilot a parent-mediated intervention for feeding challenges in children with autism building on recent research and current successful models already being used. A parent-mediated intervention would primarily occur in the home environment, working with the parent to establish goals and implement the intervention based on their child's specific needs.

NCT ID: NCT02917278 Completed - Hemodialysis Clinical Trials

Pilot Study of Nutrition in Maintenance Hemodialysis Patients

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

This pilot study aims to produce preliminary data on the safety of providing high-protein meals to patients during dialysis, and effects of this intervention on nutritional status and quality of life outcomes. This is a non-randomized, parallel arm study. Meals provided will follow recommended dietary guidelines for HD patients and will provide approximately 1/3 of daily recommended protein intake. Patients will be allocated to either the treatment or control group by HD shift schedule. 2 months of baseline data will be collected, followed by 9 weeks of meal intervention/control and data collection. The primary outcome will be frequency of hypotensive events during dialysis requiring intervention. Secondary outcomes will include highest and lowest systolic blood pressure during dialysis, blood biochemistries including measures of renal function, nutritional status, and electrolyte balance; dialysis compliance; fluid retention; sleep and other quality of life measures; and dietary intake data.

NCT ID: NCT02309840 Completed - Food Habits Clinical Trials

The Modifying Eating and Lifestyles at School Study

MEALS
Start date: September 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the impact of introducing healthier, chef-enhanced foods and/or environmental modifications (choice architecture) on selection and consumption of school foods among elementary and middle school students.

NCT ID: NCT02298790 Completed - Obesity Clinical Trials

Effect of Dietary Habits on Metabolic Health

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

The goal of this application is to understand the connection between people's eating habits and the risk for developing diabetes, obesity, and cardiovascular disease.

NCT ID: NCT02007551 Completed - Social Isolation Clinical Trials

Evaluating the RelAte Mealtime Program as an Intervention to Treat Social Isolation and Improve Cooking Behaviour Among Older Adults Living Alone

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

The purpose of this study is to evaluate the impact of a psychosocial and nutritional intervention, entitled "RelAte", on cooking and mealtime behaviours of older adults who are living alone and at risk of social isolation. The intervention will be delivered in the home of participants by a trained volunteer of a similar age.

NCT ID: NCT01866280 Completed - Sleep Clinical Trials

Sleep Timing and Energy Balance

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

The purpose of this study is to test the effects of sleep and meal timing, independent of sleep duration, on glucose regulation and metabolic and hormonal control of energy balance in normal weight adults. This study will be a 4-phase, randomized controlled study of 5 days each in which participants will undergo 2 phases of late sleep times that differ in meal timing (normal or late) and 2 phases of normal sleep times that differ in meal timing (normal or late). The Aims and Hypotheses of this study are: Aim 1: To compare hormonal regulation of food intake and metabolic risk markers in response to altered sleep and meal timing. - Hypothesis 1: There will be an interaction between sleep and meal time on glucose, insulin, and glucose and insulin area under the curve after the glucose tolerance test such that the late sleep/late meal will result in the worst metabolic profile, normal sleep/late meal and late sleep/normal meal will have an intermediate profile, and normal sleep/normal meal will result in the best metabolic profile. - Hypothesis 2: There will be an interaction between sleep and meal time on leptin and ghrelin concentrations such that the late sleep/late meal timing phase will result in low leptin/high ghrelin, normal sleep/late meal timing and late sleep/normal meal will have an intermediate profile, and normal sleep/normal meal timing will result in high leptin/low ghrelin. Aim 2: To compare food intake over a 24-h period in response to altered sleep and meal timing. • Hypothesis 3: Energy and fat intakes will be greater during the late sleep timing phase compared to normal sleep timing.