A nationwide, prospective collection of patient reported outcomes in the Cancer Registry of Norway
Background: The Cancer Registry of Norway (CRN) has collected data on all Norwegian cancer patients from health providers since 1952. To assess cancer patients' self-reported late effects and health related quality of life(HRQoL) after treatment, the CRN started collecting data on Patient Repor...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
Norsk Forening for Epidemiologi,
2022-10-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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