21 results match your criteria: "Center for Research and Intervention on Suicide[Affiliation]"

Background: Social anxiety disorder (SAD) is one of the most prevalent anxiety disorders in Canada. Viable therapy options for the treatment of SAD include CBT being delivered virtually. In Australia, an innovative internet-delivered cognitive-behavioral therapy (iCBT) program for social anxiety has been developed, implemented, and demonstrated as effective.

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Intentional presence and the accompaniment of dying patients.

Med Health Care Philos

September 2023

Réseau Québécois de Recherche en Soins Palliatifs Et de Fin de Vie, Québec, Canada.

In this paper, we offer a phenomenological and hermeneutical perspective on the presence of clinicians who care for the suffering and dying patients in the context of end-of-life care. Clinician presence is described as a way of (1) being present to the patient and to oneself, (2) being in the present moment, and (3) receiving and giving a presence (in the sense of a gift). We discuss how presence is a way of restoring human beings' relational and dialogical nature.

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Background: Some studies suggest that individuals having lost a loved one during the COVID-19 pandemic report higher levels of grief reactions than people bereaved from natural causes. Little is known about the lived and subjective experience of individuals who lost a loved one under confinement measures.

Aim: This research aims to provide a phenomenological description of pandemic grief (PG) that can be useful in clinical settings and bereavement services.

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Article Synopsis
  • The COVID-19 pandemic significantly altered the end-of-life experiences for family caregivers, who faced challenges like restricted visitation that led to difficult ethical decisions.
  • A study involving interviews with twenty bereaved caregivers revealed they grappled with multiple responsibilities, leading to emotional distress, categorized into three main themes: collective responsibility struggles, relational conflicts, and personal sacrifices.
  • The findings are analyzed through a framework that encompasses ethical, humanistic, and existential perspectives, offering insights into the complex nature of caregiving during this crisis.
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Purpose: The COVID-19 pandemic has disrupted thousands of individuals' experience of caregiving and grief. This qualitative study aimed to gain in-dept understanding of family caregivers' lived experiences of caregiving and bereavement in the context of the COVID-19 pandemic in Quebec, Canada. The study also aimed at providing new insight about caregiving and bereavement by analysing the metaphors family caregivers use to report their experiences.

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War metaphors are omnipresent in public and medical discourse on cancer . If some studies suggest that cancer patients may view their experiences as afight, few studies focus on the metaphors that patients create from their subjective experiences. The aim was to better understand the experience of four women with incurabale metastatic breast cancer from the metaphors they used in personal cancer blogs.

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Article Synopsis
  • Palliative care clinicians work with patients nearing the end of life, often experiencing their own suffering due to compassion fatigue, vicarious trauma, and burnout.
  • The study utilized Interpretative Phenomenological Analysis (IPA) to explore the complex experiences of 21 specialized clinicians, identifying three key themes of suffering: 1) suffering as powerlessness, 2) suffering as non-recognition, and 3) easing suffering through the promise of recognition.
  • The findings suggest a need for supportive initiatives to promote recognition and well-being among palliative care clinicians at personal, professional, and institutional levels.
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An essential component of palliative care (PC) is providing psychological and existential support to the family caregivers. However, there is scant research on the existential journeys of family caregivers throughout the disease trajectory and beyond. This study aimed to obtain a deep understanding of the existential journeys of family caregivers from prognosis notification until after the death.

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