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Under 16 Cancer Patient Experience Survey

Aims to understand the experiences of cancer and tumour care among children and their parents/carers.

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
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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

Link to standard

Documentation
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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