'Kids need to talk too': inclusive practices for children's healthcare education and participation
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Published on: January 12, 2018
Donna Koller1,2
1Early Childhood Studies, Ryerson University, Toronto, ON, Canada.
Aims And Objectives:
To examine how children with chronic medical conditions view healthcare education and decision-making and to propose the application of the universal design for learning in paediatric settings.
Background:
Children and adolescents with chronic medical conditions tend to be excluded from healthcare decision-making. In schools, the universal design for learning promotes access to education and participation in school communities for all children, regardless of their disabilities or medical needs, rendering it an appropriate model for children's participation in healthcare decision-making.
Design:
This article presents findings from a qualitative study with 26 children and adolescents with chronic medical conditions about their views and experiences with healthcare education and decision-making.
Methods:
Twenty-six children and adolescents with chronic medical conditions were interviewed using semi-structured interviews.
Results:
Findings provide evidence that clinical practices often fail to provide equal opportunities for paediatric patients to understand their condition, share their views and/or participate in decisions regarding their care.
Conclusions:
In response to ongoing concerns about paediatric decision-making, we propose that the universal design for learning be adapted in paediatrics. The model presents exemplary programmes as inclusive, accounting for the needs of all children through multiple means of engagement and expression.
Relevance To Clinical Practice:
A discussion of how the principles of universal design for learning could be applied in paediatric settings is offered for the purpose of advancing ethical and psychosocial care for all children regardless of their age, developmental capacity or condition.
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