4.6 Article

Protocol of an implementation study of a clinician intervention to reduce fear of recurrence in cancer survivors (CIFeR_2 implementation study)

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BMC MEDICAL EDUCATION
卷 23, 期 1, 页码 -

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BMC
DOI: 10.1186/s12909-023-04279-0

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Cancer; Breast Cancer; Fear of Cancer recurrence; Psycho-Oncology; Communication; Clinician intervention; Training

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The study aims to explore the barriers and facilitators to implementing a low-cost brief intervention (CIFeR) to reduce fear of cancer recurrence (FCR) in routine oncology practice in Australia. The primary objective is to assess the adoption of CIFeR in routine clinical practice, while secondary objectives include identifying the uptake and sustainability, acceptability, feasibility, costs, barriers, and facilitators of CIFeR implementation, as well as assessing the impact of CIFeR training on clinicians' self-efficacy in managing FCR.
BackgroundFear of cancer recurrence (FCR) affects 50-70% of cancer survivors with 30% reporting an unmet need for help with managing FCR. Patients indicate desire to discuss FCR with clinicians, however clinicians indicate discomfort with managing FCR and no formal educational interventions on how to discuss FCR or worry exists for oncology clinicians. Our team developed a novel clinician-driven brief education intervention to help patients manage FCR (the Clinician Intervention to Reduce Fear of Recurrence (CIFeR) intervention). In earlier work, we demonstrated the feasibility, acceptability, and efficacy of CIFeR in reducing FCR in breast cancer patients. We now aim to explore the barriers and facilitators to implementing this low-cost brief intervention within routine oncology practice in Australia. The primary objective is to assess the adoption of CIFeR in routine clinical practice. Secondary objectives are to identify the uptake and sustainability, perceived acceptability, feasibility, costs, barriers and facilitators of implementation of CIFeR in routine clinical practice, and to assess whether training in CIFeR increases clinicians' self-efficacy in managing FCR with their patients.MethodsThis multicentre, single-arm Phase I/II implementation study will recruit medical and radiation oncologists and oncology surgeons who treat women with early breast cancer. Participants will complete online CIFeR training. They will then be asked to use CIFeR with suitable patients for the next 6 months. Participants will complete questionnaires prior to, immediately after and 3 and 6 months after training to assess confidence addressing FCR, and 3 and 6 months after training to assess Proctor Implementation outcomes. At 6 months, they will also be asked to participate in a semi-structured telephone interview to elicit their feedback about barriers and facilitators to using CIFeR in routine clinical practice.DiscussionThis study will provide further data to support the routine use of an evidence-based, clinician-lead educational intervention to reduce FCR in breast cancer patients. Additionally, this study will identify any barriers and facilitators to implementing the CIFeR intervention in routine care and evidence for integration of FCR training into oncology communication skills education.Trial sponsorChris O'Brien Lifehouse.Protocol version2.6, Dated 28th February 2023.

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