TY - JOUR
T1 - Brain Research to Ameliorate Impaired Neurodevelopment - Home-based Intervention Trial (BRAIN-HIT)
AU - Wallander, Jan L.
AU - McClure, Elizabeth
AU - Biasini, Fred
AU - Goudar, Shivaprasad S.
AU - Pasha, Omrana
AU - Chomba, Elwyn
AU - Shearer, Darlene
AU - Wright, Linda
AU - Thorsten, Vanessa
AU - Chakraborty, Hrishikesh
AU - Dhaded, Sangappa M.
AU - Mahantshetti, Niranjana S.
AU - Bellad, Roopa M.
AU - Abbasi, Zahid
AU - Carlo, Waldemar
N1 - Funding Information:
Funded by grants from Eunice K Eunice Kennedy Shriver National Institute of Child Health and Human Development (HD43464, HD42372, HD40607, HD40636) and the Fogarty International Center (R21 TW006703-02), and by the Division of Neonatology, Department of Pediatrics, University of Alabama at Birmingham. BRAIN-HIT Investigators include: India: Belgaum; Roopa M. Bellad, J.N. Medical College, Belgaum; Sangappa M. Dhaded, J N Medical College, Belgaum; Prab-hakar Kore, J N Medical College, Belgaum; Niranjana S. Mahantshetti, J N Medical College, Belgaum; Shivaprasad S. Goudar, J N Medical College; Pakistan: Omrana Pasha, Aga Khan University, Karachi, Zahid Abbasi, Aga Khan University, Karachi; Zambia: Elwyn Chomba, University Teaching Hospital, Lusaka; United States: Fred Biasini, University of Alabama at Birmingham; Waldemar Carlo, University of Alabama at Birmingham; Hrishikesh Chakraborty, RTI International, Durham, North Carolina; Richard J. Derman, Christiana Care, Wilmington, Delaware; Robert L. Goldenberg, Drexel University; Elizabeth McClure, RTI International, Durham, North Carolina; Darlene Shearer, Western Kentucky University; Vanessa Thorsten, RTI International, Durham, North Carolina; Jan L. Wal-lander, University of California, Merced; Linda L. Wright, NICHD;
Funding Information:
This project has been funded by the Fogarty International Center and is currently being funded by the Eunice K Eunice Kennedy Shriver National Institute on Child Health and Human Development, both of the National Institutes of Health in the U.S.. The authors of this paper have no competing interests to declare.
PY - 2010/4/30
Y1 - 2010/4/30
N2 - Background: This randomized controlled trial aims to evaluate the effects of an early developmental intervention program on the development of young children in low- and low-middle-income countries who are at risk for neurodevelopmental disability because of birth asphyxia. A group of children without perinatal complications are evaluated in the same protocol to compare the effects of early developmental intervention in healthy infants in the same communities. Birth asphyxia is the leading specific cause of neonatal mortality in low- and low-middle-income countries and is also the main cause of neonatal and long-term morbidity including mental retardation, cerebral palsy, and other neurodevelopmental disorders. Mortality and morbidity from birth asphyxia disproportionately affect more infants in low- and low-middle-income countries, particularly those from the lowest socioeconomic groups. There is evidence that relatively inexpensive programs of early developmental intervention, delivered during home visit by parent trainers, are capable of improving neurodevelopment in infants following brain insult due to birth asphyxia.Methods/Design: This trial is a block-randomized controlled trial that has enrolled 174 children with birth asphyxia and 257 without perinatal complications, comparing early developmental intervention plus health and safety counseling to the control intervention receiving health and safety counseling only, in sites in India, Pakistan, and Zambia. The interventions are delivered in home visits every two weeks by parent trainers from 2 weeks after birth until age 36 months. The primary outcome of the trial is cognitive development, and secondary outcomes include social-emotional and motor development. Child, parent, and family characteristics and number of home visits completed are evaluated as moderating factors.Discussion: The trial is supervised by a trial steering committee, and an independent data monitoring committee monitors the trial. Findings from this trial have the potential to inform about strategies for reducing neurodevelopmental disabilities in at-risk young children in low and middle income countries.Trial Registration: Clinicaltrials.gov NCT00639184.
AB - Background: This randomized controlled trial aims to evaluate the effects of an early developmental intervention program on the development of young children in low- and low-middle-income countries who are at risk for neurodevelopmental disability because of birth asphyxia. A group of children without perinatal complications are evaluated in the same protocol to compare the effects of early developmental intervention in healthy infants in the same communities. Birth asphyxia is the leading specific cause of neonatal mortality in low- and low-middle-income countries and is also the main cause of neonatal and long-term morbidity including mental retardation, cerebral palsy, and other neurodevelopmental disorders. Mortality and morbidity from birth asphyxia disproportionately affect more infants in low- and low-middle-income countries, particularly those from the lowest socioeconomic groups. There is evidence that relatively inexpensive programs of early developmental intervention, delivered during home visit by parent trainers, are capable of improving neurodevelopment in infants following brain insult due to birth asphyxia.Methods/Design: This trial is a block-randomized controlled trial that has enrolled 174 children with birth asphyxia and 257 without perinatal complications, comparing early developmental intervention plus health and safety counseling to the control intervention receiving health and safety counseling only, in sites in India, Pakistan, and Zambia. The interventions are delivered in home visits every two weeks by parent trainers from 2 weeks after birth until age 36 months. The primary outcome of the trial is cognitive development, and secondary outcomes include social-emotional and motor development. Child, parent, and family characteristics and number of home visits completed are evaluated as moderating factors.Discussion: The trial is supervised by a trial steering committee, and an independent data monitoring committee monitors the trial. Findings from this trial have the potential to inform about strategies for reducing neurodevelopmental disabilities in at-risk young children in low and middle income countries.Trial Registration: Clinicaltrials.gov NCT00639184.
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U2 - 10.1186/1471-2431-10-27
DO - 10.1186/1471-2431-10-27
M3 - Article
C2 - 20433740
AN - SCOPUS:77953333936
SN - 1471-2431
VL - 10
JO - BMC pediatrics
JF - BMC pediatrics
M1 - 27
ER -