How will cancer survivors use survivorship care plans?

Authors

  • Nicole A. Kinnane Australian Cancer Survivorship Centre, a Richard Pratt Legacy, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia
  • Amanda J. Piper Australian Cancer Survivorship Centre, a Richard Pratt Legacy, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia
  • Michael Jefford Australian Cancer Survivorship Centre, a Richard Pratt Legacy, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia; ;Department of Cancer Experiences Research, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia; ;Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, Victoria, Australia

DOI:

https://doi.org/10.1080/0284186X.2016.1266082

Abstract

Background: Survivorship care plans (SCPs) are internationally endorsed as an important tool to enhance post-treatment survivorship care. To support broad implementation of SCPs, we investigated survivors’ preferences regarding SCPs.

Material and methods: The study was conducted at a comprehensive cancer center. Eligible patients from 10 clinical services, generally up to 12 months following end of treatment (EOT) were approached in clinics or via telephone. A purpose-designed survey assessed survivors’ intended use of a SCP and preferences regarding format and content. Intended minimum sample size of 200.

Results: Two hundred and thirty surveys were returned (response rate 68%). Of the 230 participants, over 55% had completed treatment within six months, 35% between six and 12 months, and 10% were receiving ongoing treatments. Most (82%) had not received a SCP and more than one third (42%) reported receiving no information resources at EOT. Almost all (98%) desired further information. Most common information elements desired in a SCP: ‘list of symptoms to watch out for and report’ (76%), ‘summary of treatment received’ (70%) and ‘things I can do to look after myself’ (67%). Most common suggested uses were as: ‘a record of cancer treatment’ (63%), ‘a reminder of things to do to look after myself ’ (57%) and ‘to help me understand my cancer experience’ (56%). Over half (52%) would share the information with their general practitioner. Most indicated preference for paper-based SCPs (91%). There was support for both brief (36%) and detailed versions (42%). Over half requested the information be delivered in a face-to-face discussion with a health professional. Regular telephone support from the treating health care team was most commonly suggested as an additional service to support survivors after EOT.

Conclusions: Although similar to international findings, results suggest alternate ways of providing the information that survivors desire. Most desired SCP elements have been defined. A flexible approach to SCP interventions is justified.

Downloads

Download data is not yet available.

Downloads

Additional Files

Published

2017-02-01

How to Cite

Kinnane, N. A. ., Piper, A. J. ., & Jefford, M. . (2017). How will cancer survivors use survivorship care plans?. Acta Oncologica, 56(2), 183–189. https://doi.org/10.1080/0284186X.2016.1266082