A clinical measure is: a published measurement tool and designed for a specific purpose and population.
Read Resources
159 resources found
Authorship Scenarios
The names and events are fictitious but were developed to initiate discussion of possible authorship dilemmas and to determine how the authorship guidelines could be applied.
Read Resources
Guidelines on authorship of abstracts, presentations and papers
To provide a clear understanding of what constitutes ‘authorship’ and the order in which authors should be recorded.
Read Resources
“If I knew then what I know now” … Parents’ Reflections on Raising Children with Cerebral Palsy
Qualitative interviews with 9 parents participating in this study in order to learn from them about their experiences parenting a child with cerebral palsy from early childhood into young adulthood.
Read Resources
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.
Read Resources
Development of a Parent Information KIT (KIT: Keeping it Together™)
The KIT: Keeping it Together™ has been designed to help these parents use information as a tool that will help them to get ‘the best’ for their child(ren).
Read Resources
Learning about the Benefits of Microboards: Danny’s Story
This was 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.
Read Resources
CP-NET Meet the Author: Amanda Leduc
CP-NET was thrilled to have disability advocate and author Amanda Leduc, speak on her book ‘Disfigured: On Fairy Tales, Disability, and Making Space’. Watch her talk about storytelling as a means of challenging ableism and celebrating all people. Followed by her…
Read Resources
F-words Knowledge Hub
In 2011, Dr. Rosenbaum and Dr. Gorter published a paper titled: “The ‘F-words’ in Childhood Disability: I swear this is how we should think!” Inspired by over two decades of CanChild research and continual discussion amongst members of the CanChild family, the paper features six F-words that…
Read Resources