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Child Development clinical trials

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NCT ID: NCT01704105 Completed - Malnutrition Clinical Trials

WASH Benefits Kenya

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

The purpose of this study is to measure the independent and combined effects of interventions that improve sanitation, water quality, handwashing, and nutrition on child health and development in the first years of life.

NCT ID: NCT01683565 Completed - Preterm Birth Clinical Trials

Preemie Tots: A Pilot Study to Understand the Effects of Prematurity in Toddlerhood

Start date: September 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to examine whether supplementation with certain polyunsaturated fatty acids can help development and behavior of children born preterm.

NCT ID: NCT01590095 Active, not recruiting - Malnutrition Clinical Trials

WASH Benefits Bangladesh

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

Brief Summary: The purpose of this study is to measure the independent and combined effects of interventions that improve water quality, sanitation, hand washing, and nutrition on child growth and development in the first years of life.

NCT ID: NCT01576783 Completed - Preterm Birth Clinical Trials

Omega Tots: A Randomized, Controlled Trial of Long-chain Polyunsaturated Fatty Acid Supplementation of Toddler Diets and Developmental Outcomes

Start date: April 26, 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to examine whether supplementation with certain polyunsaturated fatty acids can help the cognitive development of children born preterm.

NCT ID: NCT01466933 Completed - Child Development Clinical Trials

Responsive Parenting Program for Infants in Rural Bangladesh

Start date: January 2011
Phase: N/A
Study type: Interventional

Children of mothers in the intervention parenting program are expected to show benefits over the standard care control group in terms of better cognitive/language development, less recent illness, and better height for age. The mothers assigned to the intervention parenting program are expected to evidence higher levels of home stimulation, better health prevention, and better dietary diversity, along with more accurate knowledge of child development.

NCT ID: NCT01343940 Completed - Child Development Clinical Trials

Strengthening Families and Reducing Risk Thru Developmental and Legal Collaboration

dulce
Start date: February 2011
Phase: Phase 2/Phase 3
Study type: Interventional

Project Dulce is designed to test a new approach to delivering family support, in the context of the primary care medical home. The target population to be served is infants between birth and 6 months old and their families who receive primary care at Boston Medical Center. A dulce family partner will reach infants and families through their routine health care visits during their first six months of life and provide them with support for unmet legal needs, screen infants for developmental problems, screen families for mental health problems, and improve families' knowledge of child development. The control group will receive training on safe sleep and safe transportation for their newborn.

NCT ID: NCT01275001 Completed - Child Development Clinical Trials

Effects of Music Intervention on the Brain Development of Preschool Children

Start date: December 2010
Phase: N/A
Study type: Observational

The purpose of this research study is to learn more about the effects a musical intervention has on typical brain development in preschool-aged children.

NCT ID: NCT00989859 Completed - Child Development Clinical Trials

Photo-Plethysmographic Camera to Monitor Heart Rate, Respiration Rate and Oxygen Saturation in Infants

Start date: September 2009
Phase:
Study type: Observational

The researchers want to determine if ambient light, plethysmographic , can monitor reliably heart rate, respiration rate and oxygen saturation in infant patients in a hospital setting.

NCT ID: NCT00980733 Recruiting - Child Development Clinical Trials

Efficacy of Micronutrient Fortified Yoghurt in School Children for Health Benefits

Start date: September 2008
Phase: Phase 3
Study type: Interventional

To evaluate the efficacy of consumption of yoghurt fortified with 30% recommended dietary allowance (RDA) of essential micronutrients (iron, zinc, vitamin A and iodine) for a period of one year in comparison to same yoghurt without fortification for change in mean levels and proportion deficient for markers of status of Iron (Hemoglobin, Serum ferritin, Serum transferrin, ZnPP), Vitamin A (Plasma retinol levels), Iodine (Urinary iodine levels), Zinc (Plasma zinc), and copper (Plasma copper levels, sub sample of children); improvement in cognitive development, reduction in episodes/days of illnesses (diarrhea, pneumonia, febrile illness), hospitalizations and morbidity causing absenteeism from school and improvement in growth. Additionally to evaluate the efficacy of consumption of fortified and non fortified yoghurt (plain yoghurt) for a period of 12 months in comparison to pure control that do not receive any intervention in the improvement in cognitive development and physical growth. The main objective is to evaluate the impact of addition of micronutrients to Yoghurt and can be best addressed by RCT. The effect of taking yoghurt per se cannot be blinded so for that the investigators have included a concurrent control. Hypothesis: Consumption of fortified yoghurt with 30% RDA of essential micronutrients (iron, zinc, vitamin A and iodine) for a period of one year will improve the micronutrient status indicators, cognitive development, and growth and reduce morbidity of children.

NCT ID: NCT00970853 Completed - Child Development Clinical Trials

MOM Program 8-Year Follow-up

Start date: March 2009
Phase: Phase 3
Study type: Interventional

Study measures will evaluate cognitive, academic, and behavioral outcomes for the children, school services received, and caregiver stress and depression. The main study outcome measures include cognitive status, school functioning, and behavior. Long-term outcomes will be studied in attempt to verify the 33 and 60 month significant differences found in school participation and behavior between the intervention and control groups.