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 Reported...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Norsk Forening for Epidemiologi
2022-10-01
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| Series: | Norsk Epidemiologi |
| Online Access: | https://www.ntnu.no/ojs/index.php/norepid/article/view/4977 |