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Colorectal cancer survivors' experiences and views of shared and telehealth models of survivorship care: A qualitative study.
Gore, Claire; Lisy, Karolina; O'Callaghan, Clare; Wood, Colin; Emery, Jon; Martin, Andrew; De Abreu Lourenco, Richard; Schofield, Penelope; Jefford, Michael.
Affiliation
  • Gore C; Department of Psychological Sciences, Swinburne University of Technology, Melbourne, Victoria, Australia.
  • Lisy K; Psychosocial Oncology Program, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
  • O'Callaghan C; Department of Health Services Research, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
  • Wood C; Australian Cancer Survivorship Centre, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
  • Emery J; Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Victoria, Australia.
  • Martin A; Departments of Psychosocial Cancer Care and Medicine, St Vincent's Hospital, The University of Melbourne, Melbourne, Victoria, Australia.
  • De Abreu Lourenco R; Department of Health Services Research, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
  • Schofield P; Centre for Cancer Research and Department of General Practice and Primary Care, University of Melbourne, Melbourne, Victoria, Australia.
  • Jefford M; National Health and Medical Research Council Clinical Trials Centre, University of Sydney, Sydney, New South Wales, Australia.
Psychooncology ; 33(1): e6265, 2024 Jan.
Article in En | MEDLINE | ID: mdl-38072641
ABSTRACT

OBJECTIVES:

The number of colorectal cancer (CRC) survivors is increasing and current models of survivorship care are unsustainable. There is a drive to implement alternative models of care including shared care between general practitioners (GPs) and hospital-based providers. The primary objective of this study was to explore perspectives on facilitators and barriers to shared care. The secondary objective was to explore experiences of telehealth-delivered care.

METHOD:

Qualitative data were collected via semi-structured interviews with participants in the Shared Care for Colorectal Cancer Survivors (SCORE) randomised controlled trial. Interviews explored patient experiences of usual and shared survivorship care during the SCORE trial. In response to the COVID pandemic, participant experiences of telehealth appointments were also explored. Interviews were recorded and transcribed for thematic analysis.

RESULTS:

Twenty survivors of CRC were interviewed with an even number in the shared and usual care arms; 14 (70%) were male. Facilitators to shared care included good relationships with GPs; convenience of GPs; good communication between providers; desire to reduce public health system pressures. Barriers included poor communication between clinicians; inaccessibility of GPs; beliefs about GP capacity; and a preference for follow-up care with the hospital after positive treatment experiences. Participants also commonly expressed a preference for telehealth-based follow-up when there was no need for a clinical examination.

CONCLUSIONS:

This is one of few studies that have explored patient experiences with shared and telehealth-based survivorship care. Findings can guide the implementation of these models, particularly around care coordination, communication, preparation, and personalised pathways of care.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Colorectal Neoplasms / Telemedicine / Cancer Survivors Limits: Female / Humans / Male Language: En Journal: Psychooncology Journal subject: NEOPLASIAS / PSICOLOGIA Year: 2024 Type: Article Affiliation country: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Colorectal Neoplasms / Telemedicine / Cancer Survivors Limits: Female / Humans / Male Language: En Journal: Psychooncology Journal subject: NEOPLASIAS / PSICOLOGIA Year: 2024 Type: Article Affiliation country: Australia