Establishing the cardiovascular risk trajectory of children with Developmental Coordination Disorder (PHAST II)
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11 resources found
Early Experiences and Participation Patterns of Children with Developmental Coordination Disorder
This is a qualitative research study intended to increase the understanding of children with Developmental Coordination Disorder (DCD) by examining the observations and experiences of their parents.
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Focus on Function
The Focus on Function Study will compare two treatment approaches (“child-focused” and “context-focused”) that are currently being used for children with cerebral palsy and other developmental and motor delays.
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Evaluation of an information KIT for parents of children with special needs: Use, utility and impact
The focus of this two-year prospective evaluation (N=500) is to determine the perceptions of impact and use of the Parent Information KIT (KIT: Keeping it Together™) in pediatric rehabilitation settings.
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Teachers’ perceptions of children with DCD
Timely and effective identification of children with DCD relies on a better understanding of teachers’ perceptions of children with motor difficulties, especially with regard to the influence of child gender, child behaviour and the type of motor problem.
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STACK
In the STACK Study (which stands for Screening, Tracking and Assessing Coordination in Kids), students in Grades 4 to 8 in two school boards were screened to identify children who may have coordination difficulties.
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Developmental Coordination Disorder: Screening and Intervention (PHAST I)
Developmental Coordination Disorder: Examination of a feasible screening and intervention for clumsy children (PHAST I)
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Life Experiences of Adolescents
Although the impact of the disorder in the early school years has been described in the research literature, less is known about the impact of DCD in the later years.
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Incidence and Prevalence of Childhood Disabilities
The report reviews a considerable volume of the English language literature published since 1990, and provides a useful review of some critical concepts about the epidemiology of childhood disabilities, as well as an overview of the disabilities with which OACRS programs are concerned.
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DCD Physician Study
This study investigated the use of an educational outreach program (using a ‘shared-care’ model) made available to 147 primary care physicians to improve the long-term management of children with DCD.
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