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Nutritional Status clinical trials

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NCT ID: NCT02779491 Completed - Nutritional Status Clinical Trials

Evaluation of a 5-a-day Fruit and Vegetable Mobile Phone Application

Start date: June 1, 2016
Phase: N/A
Study type: Interventional

This is a randomized controlled trial to assess the impact of a novel fruit and vegetable mobile phone application on fruit and vegetable intakes, knowledge and attitudes.

NCT ID: NCT02592109 Completed - Overweight Clinical Trials

Effect of Enhanced Counseling Using Complementary Feeding Recommendation Based on Linear Programming on Nutritional Status,Omega-3 Fatty Acids, Malondialdehyde, and Alpha-Tocopherol in Overweight Children in East Jakarta

Start date: November 2015
Phase: Phase 2
Study type: Interventional

The epidemic of pediatric obesity has become a public health burden in both developed and developing countries, due to its serious health consequences, including an increased risk of type 2 Diabetes Mellitus and heart disease. Currently, dietary and exercise changes are still the center of preventive and treatment measures of obesity. Recently, the omega-3 group, one of the groups of polyunsaturated fatty acids (PUFAs), has been associated with many positive effects leading to the improvement of many diseases related to obesity. Nevertheless, the consumption of this essential nutrient requires certain ration to optimize its favorable result. Although previous studies have examined the efficacy of dietary counseling approach as treatment for obesity, none of them as explicitly explore the use of linear programming to create a tailored diet containing high omega-3 fatty acid food as a part of dietary counseling in obesity management program among children. Thus, this study is intended to contribute the clinical evidence regarding this area of knowledge, specifically the effects of enhanced counseling containing complementary feeding recommendation on nutritional status, omega-3 fatty acid, malondialdehyde, and alpha Tocopherol among children with risk of overweight aged 12 -23 months in East Jakarta.

NCT ID: NCT02589704 Completed - Nutritional Status Clinical Trials

Nutritional Status of Cerebral Palsy Patients in Turkey

Start date: November 2015
Phase: N/A
Study type: Observational

This is a single visit, non-interventional, cross sectional study about risk factors, etiology, nutritional status and feeding methods in CP patients.

NCT ID: NCT02583880 Completed - Malnutrition Clinical Trials

Screening Day Latin America

Start date: October 2015
Phase: N/A
Study type: Observational

This is a survey which will be performed on a specific day (the "Screening Day") in Latin American ICUs. In eligible patients who receive enteral or parenteral nutrition a retrospective calculation of the "caloric deficit" will be performed. The caloric deficit is the difference between energy target of each patient and actually administered calories.

NCT ID: NCT02201225 Completed - Nutritional Status Clinical Trials

A Methodology Study to Evaluate a Sitting Knee Measuring Device in Assessing Growth in Indian Children.

Start date: October 1, 2014
Phase: Phase 1
Study type: Interventional

This methodology study will evaluate the sensitivity in using sitting knee digital caliper to measure changes in sitting knee length from over a 12-week study period amidst children in the age of 6 to 12 years in a community-based study in children ages 6 to 12 years who are receiving nutritional supplementation with micronutrients or without micronutrients.

NCT ID: NCT02094781 Completed - Nutritional Status Clinical Trials

Effect of Using Whey Protein and Creatine Supplements on Muscular Strength in Weight-training Adult Males

Start date: December 2013
Phase: Phase 1
Study type: Interventional

The purpose of this study was to evaluate the effect of combined whey protein and creatine supplement, as compared with whey protein supplement alone, on change in upper and lower body strength.

NCT ID: NCT02058654 Completed - Nutritional Status Clinical Trials

A Clinical Study to Investigate the Effects of Creatine Supplementation on Muscle Energetics and Cognitive Function in Young Healthy Male Athletes and an Ageing Population

Start date: December 1, 2013
Phase: Phase 1
Study type: Interventional

This study will examine the impact of creatine supplementation on muscle function and cognitive performance in young and older subjects.

NCT ID: NCT01944891 Completed - Diet Clinical Trials

Diet and Nutritional Status of Adolescent Girls in Zambézia, Mozambique

ZANE
Start date: January 2010
Phase: N/A
Study type: Observational

Data on the diet and nutritional status of adolescent girls in Zambézia Province, Mozambique was collected. A cross-sectional study was carried out in 2010 in two seasons, January-February and May-June. Participants (total n=551) were recruited from Quelimane (the provincial capital), Maganja da Costa district and Morrumbala district.

NCT ID: NCT01584661 Not yet recruiting - Nutritional Status Clinical Trials

The Continuity of Nutritional Care Among Elderly Patients

Start date: July 2012
Phase: N/A
Study type: Observational

Objectives: 1. To determine the level of compliance with nutritional recommendations (dietary and nutritional supplements) following discharge from hospitalization; 2. To identify barriers for post-discharge adherence to professional nutritional recommendations; 3. To determine the impact of adherence (high vs. low) to the nutritional treatment guidelines on functional and health indicators. Working hypothesis: High adherence to nutritional care after hospitalization will be associated with better functional and health outcomes.

NCT ID: NCT01492946 Completed - Nutritional Status Clinical Trials

Impaired Preoperative Nutritional Status as a Risk Factor for Postoperative Clinical Outcome

PreopBIA
Start date: May 2010
Phase: N/A
Study type: Observational

The aim of this retrospective observational study is to determine the impact of preoperative nutritional status on postoperative outcome. Elective surgical patients were screened with Bio-Impedance-Analysis, Malnutritional Universal Screening Tool, and other variables for body composition. Outcome parameters were collected by patient chart review.