Young cancer patients survey finds improvement in NHS communication

A survey of children’s experience of cancer care has found improvements in NHS communication and information along with areas in need of improvement – including in the diagnostic process and privacy in hospitals.

(c) National Cancer Institute

(c) National Cancer Institute

The under 16 cancer patient survey was conducted by healthcare research charity Picker on behalf of NHS England.

Over four in five (82%) of parents or carers reported they could ‘definitely' find information about their child's diagnosis in 2024 – a sizeable improvement from 72% in 2023.

Over three quarters (77%) of parents or carers said that hospital staff were ‘always' sensitive when discussing information in front of their child (up from 71% in 2023), and 80% felt staff always shared information with children in an appropriate way (up from 76% in 2023).

There were also improvements around privacy in hospitals – although a large proportion of parents, carers, and children still reported concerns. In 2024, 57% said that they ‘always' had somewhere private to talk to staff when in hospital, an increase from 50% in both 2023 and 2022.

Areas for improvement included the proportion of children who felt that hospital staff ‘always' talked to them, not just their parent or carer, decreased from 78% in 2023 to 71% in 2024.

Only 70% of parents or carers reported they were definitely told about their child's cancer or tumour diagnosis in a sensitive way.

Similarly, 71% of parents or carers felt they were seen at the hospital as soon as they thought was necessary after being referred by their GP.

Three quarters (75%) of parents, carers and children reported information at diagnosis was definitely given in a way they could understand.

Amy Tallett, Picker's head of research, said: ‘As the Government continues to develop its National Cancer Plan, these results should be used by providers to understand care quality from the perspective of young patients and their parents – and this insight should be used to guide improvements in the things that matter most to people affected by childhood cancers. At a national level, these results provide robust evidence about priorities for the upcoming cancer plan and as the 10-Year Plan is implemented. Listening to and acting on feedback from young patients and their families is vital to ensuring high quality person centred care for all.'

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