Table 2.
• Summary of the study design and methods in each of the six research projects | |
• Challenges in involving young people in research: | |
▪ Graphs of recruitment to the cohort [16] | |
▪ Summary of the analysis of screening log data from the cohorta | |
▪ Young people’s perspectives of having access to research [27] | |
▪ Challenges healthcare professionals faced in recruiting to the cohort [30] | |
• Delivery of information and communication [31] | |
▪ Cohort wave 1 results: not being given time to decide about fertility preservationa | |
▪ Cohort wave 1 results: how young people found out that they had cancera | |
• Empowering young people gives you information you would not have thought to ask [31] | |
• The continuing impact of cancer after treatment has ended and young people are living beyond their diagnosis [31] | |
• The impact of a cancer diagnosis on carers [25]a | |
• Young people’s reported experience of being treated on an adult, children or TYA specialist cancer ward [31]a | |
• The environment of care [23]a | |
• Cohort wave 1 results: the best and worst aspects of carea | |
• Sexuality and cancer [29] | |
• The value and importance of the TYA workforce [21]a |
ainclusion of unpublished data