Under 16 Cancer Patient Experience Survey
Aims to understand the experiences of cancer and tumour care among children and their parents/carers.
Contents
- Documentation
About this standard
- Publisher
- NHS England
- Also known as
- Under 16 Cancer Patient Experience Survey 2020-23
- Reference code
- DCB3131 Amd 65/2020
- Publication date
- 11/12/2020
- Status
- Active
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Active. Active standards are stable, maintained and have been approved, assured or endorsed for use by qualified bodies.
Deprecated Deprecated standards are available for use and are maintained, but are being phased out, so new functionality will not be added.
Retired standards Retired standards are not being maintained or supported and should not be used.
- Standard type
- Collections
Show definitions of standard types
Collections. A Collection is a systematic gathering of a specified selection of data or information for a particular stated purpose from existing records held within health and care systems and electronic devices.
Extractions. An extraction is a type of collection that is pulled from an operational system by the data controller and transmitted to the receiver without additional processing or transcription by the sender.
Information standards. Information standards are agreed ways of doing something, written down as a set of precise criteria so they can be used as rules, guidelines, or definitions.
Technical Standards and specifications. Technical standards and specifications specify how to make information available technically including how the data is structured and transported.
- Collection level
Record level
- Frequency
Dataset publication or collection occurs once a year.
- Contact point
Using this standard
- Applies to
- Thirteen Principal Treatment Centres (PTCs) based within sixteen Trusts in England
Topics and care settings
- Topic
- Care
- Child
- Service
- Care setting
- Hospital
Legal basis and endorsements
- Legal authority
Section 250 of the Health and Social Care Act 2012
This standard is published under section 250 of the Health and Social Care Act 2012.
More information
This data collection supports a new voluntary annual survey asking cancer patients under the age of 16 with a confirmed primary diagnosis of cancer or tumour and who have recently received NHS care and/or treatment, and their parents/ carers, for feedback on children’s cancer services.
The results will help improve children’s cancer services across England.
Page last updated: 15 April 2024