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Hunger clinical trials

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NCT ID: NCT03656146 Completed - Hunger Clinical Trials

Food for Thought: Food Insecurity Screening in the Emergency Department

Start date: May 15, 2017
Phase: N/A
Study type: Interventional

This study compares food insecurity disclosure rates in face-to-face interviews versus electronic formats, and explores caregiver preferences regarding screening modality and location, in a large, urban pediatric emergency department. Half of the participants were screened for food insecurity verbally, face-to-face by a research assistant, and half of the participants were screened electronically by a tablet.

NCT ID: NCT03537781 Recruiting - Food Preferences Clinical Trials

The Effect of Food Labelling and Satiety on Individuals Food Choice

Start date: June 12, 2018
Phase: N/A
Study type: Interventional

Previous research has shown that nutritional knowledge is a key indicator in healthy eating choices, but real-life examinations of the associations between both nutritional knowledge and state of hunger and satiety on individuals' food choice of healthy vs unhealthy snacks is limited. The present study aims to investigate whether the presence of nutritional information on food labels will affect participants' food choice when hungry and when satiated.

NCT ID: NCT03489226 Completed - Hunger Clinical Trials

Capsimax Effect on Metabolic Rate, Satiety and Food Intake

Start date: May 2, 2016
Phase: N/A
Study type: Interventional

Comparison of Capsimax™ 2mg and 4mg of capsicum extract vs. placebo on metabolic rate and satiety.

NCT ID: NCT03472703 Completed - Eating Behavior Clinical Trials

Effect of Consumption on Cognitive Processes

Start date: July 1, 2017
Phase: N/A
Study type: Interventional

To get a better understanding of the interaction between metabolism, neural responses, cognitive processes and appetite the investigaters will examine the effect of food consumption on cognitive processes. The investigaters will look at the effect of satiation on cognitive performance on both a behavioural and neuronal level. In this study participants will undergo functional magnetic resonance imaging (fMRI) measurements while performing a food reward and inhibition task, and in addition perform a memory, working memory and delay discount task, once when hungry and once when full.

NCT ID: NCT03387345 Completed - Blood Glucose Clinical Trials

Barley and Rice Mixture Effects on Blood Glucose

Start date: February 13, 2017
Phase: N/A
Study type: Interventional

The purpose of this research was to investigate 5 different formulations of whole grain barley and refined white rice against a control of white bread on post-prandial glycemic response, as well as self-reported hunger/satiety in a randomized cross-over trial.

NCT ID: NCT03227900 Completed - Hunger Clinical Trials

Lidocaine and Food Intake

Start date: July 19, 2017
Phase: Phase 4
Study type: Interventional

World's population over 60 years old is increasing rapidly. It is expected that in 2050 elderly population will be 22% of the total population, representing around 2 billion people. This situation means a rising in the incidence of elderly-related diseases, and thereby the need for long-term care. Reduction in body fat and weight are a common problem among the institutionalized elderly. Some factors that contribute to the anorexia of aging are decreased perception of hunger and increased satiation. This represents an increased risk of developing cachexia even during minor illnesses. The potentially severe consequences of anorexia of aging a greater understanding of the underlying mechanism of these changes is highly important. Intraesophageal and intragastric infusion of 20mg/kg lidocaine results in an increase in food intake in Wistar rats. All infusions were done 30 minutes before the start of the meal intake (meal consisted of mealworms). It may be possible to decrease satiation, increase hunger, and hence food intake in elderly individuals through gastric infusion of the anesthetics lidocaine or benzocaine. In the future this study could potentially contribute to improve food intake in elderly vulnerable of losing body weight. Therefore, the current study aims to investigate the effect of intragastric administration of lidocaine on food intake, satiety/satiation and gastrointestinal complaints.

NCT ID: NCT03173794 Withdrawn - Clinical trials for Patient Satisfaction

CommunityRx for Hunger: A Hospital-Based Intervention

Start date: April 2018
Phase: N/A
Study type: Interventional

The goal of this research program is to reduce health disparities by deploying an information-based intervention to increase caregiver utilization of community-based food supports and satisfaction with care among food insecure caregivers of hospitalized children. We will conduct a randomized controlled trial to evaluate, versus usual care, the effects of the CommunityRx-H intervention on caregiver use of food resources (primary), caregiver patient satisfaction with care (primary), caregiver mental health-related quality of life (secondary), and caregiver household food security (secondary). The proposed research will yield an understanding of how to leverage a child's hospitalization to effectively intervene on the problem of food insecurity. Findings will inform the rapidly growing field of healthcare-based interventions to address health-related social needs.

NCT ID: NCT03142464 Completed - Clinical trials for Postoperative Nausea

Intravenous Fluids After Laparoscopic Cholecystectomy

Start date: July 1, 2015
Phase: N/A
Study type: Interventional

Perioperative intravenous fluid (IV) administration has been the standard procedure since 1832 and, is a widely used practice sometimes under inadequate criteria. The present work aims at verifying the clinical need that justifies the common IV fluid prescription on the postoperative (PO) period in patients undergoing videolaparoscopic cholecystectomy (CVL) elective.

NCT ID: NCT02948816 Completed - Sedentary Lifestyle Clinical Trials

The Effects of Social Media on Food Intake and Behaviour

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

Participants will be exposed to 3 conditions, in random order: 1. A Facebook page where 70% of posts are related to food. 2. A Facebook page where only 20% of posts are related to food. 3. A control condition (colouring quietly). During each of the above conditions participants will be provided with identical snacks. The snacks will be weighed before and after each condition, to determine whether there is a change in food intake across the 3 conditions.

NCT ID: NCT02827318 Completed - Hunger Clinical Trials

Eating Disinhibition and Vagal Tone and the Postprandial Response to Glycaemic Load

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

Reducing the glycaemic load (GL) of the diet may benefit appetite control but its utility is complicated by psychological influences on eating. Disinhibited behaviour, a risk factor for overconsumption, is characterized by reduced prefrontal cortex activity, which in turn directly modulates vagal tone; a phenomenon inversely associated with blood glucose (BG) and insulin levels. This double blind randomised controlled trial explores the influence of disinhibited eating and vagal tone (heart rate variability) on the postprandial response to GL and hunger.