Abstract

On behalf of the Canadian Association of Psychosocial Oncology, we are pleased to present the s from the 2021 Annual Conference, titled “Advocating for All: Psychosocial Oncology at the Intersections of Equity, Diversity, and Inclusion”. The Conference was held virtually from 8 June 2021 to 10 June 2021. This conference brought together key stakeholders including multidisciplinary professionals from nursing, psychology, psychiatry, social work, spiritual care, nutrition, medicine, rehabilitation medicine, occupational health and radiation therapy for both adult and pediatric populations. Participants included clinicians, researchers, educators in cancer care, community-based organizations and patient representatives. Patients, caregivers and family members presented abstracts that speak to their role in managing cancer experiences and care. Over one hundred (100) abstracts were selected for presentation as symposia, 20-min oral presentations, 10-min oral presentations, 90-min workshops and poster presentations. We congratulate all the presenters on their research work and contribution.

Highlights

  • Impact on Practice or Results Four key points were grouped according to data gathered: (1) why cultural adaptation of psychosocial interventions is needed in Indigenous health; (2) what it means to ethically engage with Indigenous peoples for health research; (3) the importance of selfdetermination in Indigenous health and research; and (4) how research can be used as a tool toward reconciliation

  • We excluded (1) children who live with cancer, since the financial burden has an impact on the parents instead; (2) nonWestern countries; (3) families of people living with cancer; and (4) health professionals who are associated with the care of patients in cancerology

  • Impact on Practice or Results Interview data analysis revealed three important themes: (1) deliberate consideration of cancer- and treatment-related effects and activity modification are often required for women with metastatic breast cancer (MBC) to be active; (2) participation in leisure physical activity (LPA) is closely linked to psychosocial well-being for many participants; and (3) engaging in LPA positively impacts symptoms, physical function, and treatment tolerance for several women with MBC

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Summary

Objectives

1. Identify barriers to psychosocial aspects of care across the cancer continuum, 2. Discuss the role of Indigenous Cancer Patient Navigation (CPN) in reducing cancer burden in Indigenous populations, 3. Demonstrate how professional practice grounded in Indigenous knowledge systems and philosophies of care can improve cancer outcomes for Indigenous people

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