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CATEGORY 1: ABORIGINAL AND/OR TORRES STRAIT ISLANDER PERSPECTIVES ON |
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Sub-categories
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Health, illness, well-being. |
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Cancer perspectives (meaning, fears, concerns, and taboos). |
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Gender-specific matters (‘Men’s Business’ and ‘Women’s Business’). |
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The connection between country, spirituality, family, community and health. |
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Spiritual practices, traditional healers, and traditional, complementary or alternative medicine therapies. |
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Knowing when to use traditional terminology (e.g. when to use ‘Aunty’ or ‘Uncle’). |
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CATEGORY 2: PREVENTION AND EARLY DETECTION: USING CULTURALLY APPROPRIATE INFORMATION TO DISCUSS
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Sub-categories
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Risk reduction (e.g. quit smoking and healthy eating). |
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Screening and immunisation (e.g. mammograms and HPV vaccination). |
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Early detection (cancer signs and symptoms, and co-morbidities). |
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CATEGORY 3: PRESENTATION, INITIAL INVESTIGATIONS AND REFERRAL)
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Sub-categories
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Using culturally relevant information to explain the reasons for diagnostic/referral investigations to the patient and their family/carer. |
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Addressing patient and family concerns about cancer and cancer treatment. |
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CATEGORY 4: DIAGNOSIS, STAGING & TREATMENT PLANNING
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Sub-categories
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Understanding factors which influence Aboriginal and/or Torres Strait Islander patients’ decisions about treatment and ongoing care. |
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Speaking in a culturally appropriate way about treatment options and the expected outcomes of these treatments. |
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Checking/knowing if the person has understood the information I have provided about the treatment plan. |
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Access to an expert with culturally appropriate knowledge in the multidisciplinary meetings (MDM). |
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Culturally appropriate resources to discuss and seek informed consent to participate in clinical trials (if clinically appropriate). |
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CATEGORY 5: TREATMENT
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Sub-categories
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Practising trauma-informed care using culturally informed approaches. |
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Understanding cultural practices in the clinical setting (e.g. touching patients and who to discuss diagnosis/prognosis with). |
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Working with families during cancer treatment and follow-up care. |
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Understanding cultural perceptions about pain experiences, relief and management. |
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Pathways/processes to work with the Aboriginal Hospital Liaison Officer/Aboriginal Health Worker during treatment and follow-up care. |
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Knowing about Indigenous-specific patient assistance programs/schemes (e.g. Close the Gap prescriptions). |
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Understanding the potential barriers to Aboriginal and/or Torres Strait Islander people accessing treatment, health services, and/or follow-up care. |
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CATEGORY 6: CARE AFTER INITIAL TREATMENT AND RECOVERY
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Sub-categories
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Developing culturally appropriate treatment summaries and/or follow-up care plans. |
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Strategies to provide culturally appropriate information about the signs and symptoms of recurrent and secondary prevention of disease. |
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Strategies to provide culturally appropriate information about healthy living after cancer treatment. |
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Information about referral options/pathways for social and emotional well-being and mental health services. |
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Processes to keep a patient’s General Practitioner updated (e.g. prognosis and a follow-up care plan). |
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CATEGORY 7: SUPPORTIVE CARE
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Sub-categories
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Using the Supportive Care Need Assessment Tool - Indigenous Patients (SCNAT-IP) to identify supportive care needs. |
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Using a culturally appropriate pain tool to better identify and manage pain. |
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Culturally appropriate supportive care services (internal and external to service). |
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Category 8: RECURRENT, RESIDUAL AND METASTATIC DISEASE
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Sub-categories
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Using culturally appropriate language to explain treatment intent, outcomes or adverse events for recurrent, residual or metastatic disease. |
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Discussing advance care planning in a culturally relevant manner with patients and their families/carers. |
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Discussing referral to palliative care with patients and their families/carers. |
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CATEGORY 9: END OF LIFE CARE
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Sub-categories
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Using culturally appropriate language when discussing death or dying. |
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Discussing cultural preferences related to practices around death and dying. |
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