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Showing results for "early life"
The aim of this project was to identify the top 10 priorities for childhood chronic conditions and disability (CCD) research from the perspectives of children and young people with lived experience, their parents and caregivers and the professionals who work with them.
The goal of a clinical quality registry is to deliver immediate gains in survival and quality of life by delivering timely feedback to practitioners, thereby ensuring every patient receives the best existing treatment. We are developing an Australian Brain Cancer Registry (ABCR) to identify, describe, and measure the impact of the variation and gaps in brain cancer care from the time of diagnosis to the end of life.
The purpose of this study is to examine the association between poverty and child mental disorders
This paper analyzes the effects of “shocks” to community-level unemployment expectations, induced by the Great Recession, on children’s mental well-being
A minority of 4- to 17-year-olds with ADHD and major depressive disorder were being treated with stimulant or antidepressant medication
This article describes the survey, the response rates achieved and the representativeness of the sample for the Young Minds Matter survey
Mental disorders should be a leading intervention point for suicide prevention both in the primary health sector and in the mental health sector specifically
The demonstrated higher risks in young people for continued harm or possible death support the need for ongoing initiatives to reduce self-harm
This study provides evidence that continued participation in playgroups is associated with better outcomes for children from disadvantaged families.
Engaging activities to help families keep kids happy and healthy during social isolation are available in an Australian app underpinned by the latest child development science.