Clinical Trials Logo

Growth clinical trials

View clinical trials related to Growth.

Filter by:

NCT ID: NCT00892983 Completed - Obesity Clinical Trials

Prevention of Overweight in Infancy

POInz
Start date: May 2009
Phase: N/A
Study type: Interventional

Obesity is one of the biggest threats to health in the 21st century. Rapid weight gain in the first year of life tends to lead to overweight in children, which in turn leads to overweight in adults. This rapid early weight gain occurs most often at weaning when eating patterns emerge. Infant sleep problems also appear to be associated with the risk of becoming overweight, and contribute to maternal post-natal depression. We propose to undertake a 4-arm randomised controlled trial to determine whether extra education and support for families around weaning and development of early food and activity habits, with or without intervention to improve infant sleep, will decrease the current risk patterns of rapid excessive early childhood weight gain in New Zealand. This would provide strong evidence for the value of such a strategy in the long term control of the obesity epidemic and its consequent complications. This is a two-year intervention with follow-ups at 3.5, 5 and 11 years of age.

NCT ID: NCT00824304 Completed - Cognitive Function Clinical Trials

Long-term Effects of Iron and Zinc Supplementation During Infancy on Cognitive Performance and Growth

FeZn_FU
Start date: July 2007
Phase: N/A
Study type: Observational

The hypotheses of this study are: 1. Compared to children who received a placebo, children who received iron or zinc or iron and zinc combined will perform better on cognitive tests and will have better growth status at ages 8 to 10 years. 2. Compared to children who received iron or zinc alone, children who received iron and zinc combined will perform differently on cognitive tests and will have different growth status at 8 ages 8 to 10 years 3. Compared to children who had poorer iron and zinc status or poorer growth status before and after supplementation during infancy, children who had better iron and zinc status or better growth status before and after supplementation during infancy will perform better on cognitive tests and will have better growth status at ages 8 to 10 years. 4. Compared to children who have lower iron and zinc status, poorer growth status, or low animal source intake at ages 8 to 10 years, children who have higher iron and zinc status, better growth status, or high animal source intake at ages 8 to 10 years will perform better on cognitive tests and will have better growth status.

NCT ID: NCT00808756 Completed - Healthy Clinical Trials

Study on Fermentable Carbohydrates in Healthy Infants

BAMBINOL
Start date: September 2008
Phase: N/A
Study type: Interventional

The purpose of this project is to study the effect of fermentable carbohydrates in the nutrition of healthy infants.

NCT ID: NCT00753818 Completed - Growth Clinical Trials

Developmental Effects of Infant Formula Supplemented With LCPUFA

Start date: n/a
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effects on visual development, growth, cognitive development, tolerance, and blood chemistry parameters in term infants fed one of four study formulas containing various levels of DHA and ARA.

NCT ID: NCT00705445 Completed - Pneumonia Clinical Trials

Evaluation of Zinc and / or Micronutrient Supplementation on Intestinal Flora, Diarrheal Disease Burden, Intestinal Mucosal Integrity and Growth Among Children of Pakistan

Start date: November 2008
Phase: Phase 2/Phase 3
Study type: Interventional

Information on the mechanisms of zinc is still in developing phase. Ecological and biological implications of long term zinc supplementation at population level requires assessment. The trial aims to assess the impact of routine supplementation of zinc among young growing children and evaluate its impact on intestinal microbial flora and relationship with gut mucosa integrity and co-morbidities.

NCT ID: NCT00655720 Completed - Growth Clinical Trials

The Effects on Growth of a Non-Routine Infant Formula

Start date: March 2006
Phase: N/A
Study type: Interventional

A study to evaluate the growth and development of term infants fed either an extensively hydrolyzed formula with probiotics, a partially hydrolyzed formula with probiotics, or an extensively hydrolyzed formula without probiotics

NCT ID: NCT00631046 Completed - Obesity Clinical Trials

Essential Fatty Acids During Complementary Feeding

EFiON
Start date: February 2008
Phase: N/A
Study type: Interventional

The objective of this intervention study is to examine the effect of n-3 LCPUFA on growth and body composition, intestinal health and microbiotic composition, immune function and risk markers for later diseases in 9-18 months old infants and toddlers.

NCT ID: NCT00625482 Completed - Mortality Clinical Trials

Sex-Differential Health Interventions In Low-Birth-Weight Infants

Start date: February 2008
Phase: N/A
Study type: Interventional

Our group has consistently found that the major interventions to reduce morbidity and mortality in low-income countries have sex-differential effects. These interventions include BCG vaccine, oral polio vaccination (OPV), and vitamin A supplementation (VAS). Low-birth-weight (LBW) children constitute the largest high-risk group in low-income countries. According to current policy, they receive OPV at birth. Current evidence suggests that a policy of providing BCG with OPV for girls and VAS instead of OPV for boys at birth may improve survival in LBW neonates. This will be tested in a large randomized trial. We experienced an unexpected cluster of deaths among boys in the VAS arm, which could be due to chance, but we decided to stop randomizing boys to OPV or VAS. Very recent evidence has suggested that low-birth-weight boys may benefit from BCG at birth as well. Hence, we have obtained ethical permission to continue the trial with randomization of boys to OPV or OPV plus BCG.

NCT ID: NCT00585403 Withdrawn - Obesity Clinical Trials

Exercise Changes to Peripheral Blood Mononuclear Cells in Children

Start date: December 2004
Phase:
Study type: Observational

The goal of this research is to determine how the peripheral immune system is altered by exercise and differences related to gender, pubertal status and health.

NCT ID: NCT00580099 Withdrawn - Growth Clinical Trials

Assisted Exercise in Prematurity; Effects and Mechanisms

Start date: February 2006
Phase: N/A
Study type: Interventional

Briefly our study is looking at the effects of 4 weeks of assisted exercise on the body composition and neurological/behavioral development of healthy growing premature infants enrolled between the ages of 30-33 weeks. It is a blinded study where the active group gets the exercise intervention and the control group is cuddled for the same amount of time -approximately 20 minutes. We get baseline data using muscle ultrasound, bone speed of sound and DEXA. We also get baseline blood samples to look at inflammatory mediators and growth hormone. Video of each subject is recorded an hour at two time points during the study to assess the babies for spontaneous activity. Nutritional intake information is collected daily and in the 4th week of the study assessments made for total energy expenditure using doubly labeled water. At this point in the study we repeat the ultrasounds and DEXA for comparison. Finally in the period just before discharge we do a complex neurological exam using the Brazelton NBAS assessment.