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. 2022 Nov 16;12(11):e063134. doi: 10.1136/bmjopen-2022-063134

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© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ.

This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.

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Flow chart of data collection after inclusion of an eligible survivor. The boxes describe for each time point the timing of data collection, the person providing data (survivor, HCP or both), the data collection instruments (Survivor Questionnaire, Treatment Summary or T1–T5 study questionnaire) and the types of outcomes collected. Depicted in blue are data collected for care, and in purple for research purposes. HCP, healthcare provider; PREMs, patient-reported experience measures; PROMs, patient-reported outcome measures; T1, time point 1; T2, time point 2; T3, time point 3; T4, time point 4; T5, time point 5.