Twenty-four children (aged 5 months to 18 years) who were admitted to a university hospital were observed for a total of 135 hours with the aim of describing their degree of participation in decisions concerning their own care.
The purpose of this study was to determine whether 3 adolescents diagnosed with cancer within the previous 3 to 6 months and between 13 and 15 years of age were capable of providing data directly regarding decision making.
This paper critiques the research literature from between 1993 and 2007 on children’s, parents and healthcare professionals’ experiences of children’s participation in consultations and decision-making within the Irish healthcare setting.
The purpose of this study is to review the research evidence for effects, positive or negative, of participation on health outcomes for children in care. A scoping review of major health and social work research databases was undertaken.
This report documents effective ways to promote young people’s meaningful participation in receiving health care services and/or basic information as a person in their own right and in a non-judgemental manner within a global context.
This is a report on the views, hopes and fears of young people, North and South, and is the outcome of a unique cross-border conference
This General Comment outlines the right of young people to express views freely and have them duly taken into account (art. 12) which is fundamental in realising adolescents’ right to health and development.
This report is based on a consultation with disabled children and young people in London in 2000. It focuses on the methods and processes of carrying out such a consultation-consent issues, how to structure consultation sessions and tools used.
“Take My Hand” report highlights young people’s experiences of, and perspectives on mental health services.
This paper outlines findings in relation to participation standards in HIQA foster care, residential care and special care inspection reports over a two-year period from 2013 to 2015.