about
Eating-related distress and need for nutritional support of families of advanced cancer patients: a nationwide survey of bereaved family membersAcculturation and Perceptions of a Good Death among Japanese Americans and Japanese Living in the United States.Development and validation of scales for attitudes, self-reported practices, difficulties and knowledge among home care nurses providing palliative care.Changes in Relatives' Perspectives on Quality of Death, Quality of Care, Pain Relief, and Caregiving Burden Before and After a Region-Based Palliative Care Intervention.Strategies for Development of Palliative Care From the Perspectives of General Population and Health Care Professionals: A Japanese Outreach Palliative Care Trial of Integrated Regional Model Study.Changes in quality of care and quality of life of outpatients with advanced cancer after a regional palliative care intervention program.Progressive development and enhancement of palliative care services in Japan: nationwide surveys of designated cancer care hospitals for three consecutive years.Independent Validation of the Japanese Version of the EORTC QLQ-C15-PAL for Patients With Advanced Cancer.Place of death and the differences in patient quality of death and dying and caregiver burden.Prevalence, associated factors and source of support concerning supportive care needs among Japanese cancer survivors.Length of home hospice care, family-perceived timing of referrals, perceived quality of care, and quality of death and dying in terminally ill cancer patients who died at home.The distress and benefit to bereaved family members of participating in a post-bereavement survey.Anxiety and depression in patients after surgery for head and neck cancer in Japan.Communication Disparity between Bereaved and Others: What Hurts Them and What is Unhelpful? - A Nationwide Study of the Cancer Bereaved.A Nationwide Survey of Quality of End-of-Life Cancer Care in Designated Cancer Centers, Inpatient Palliative Care Units, and Home Hospices in Japan: The J-HOPE Study.The importance of good death components among cancer patients, the general population, oncologists, and oncology nurses in Japan: patients prefer "fighting against cancer".Development and validation of the Comprehensive Quality of Life Outcome (CoQoLo) inventory for patients with advanced cancer."What I Did for My Loved One Is More Important than Whether We Talked About Death": A Nationwide Survey of Bereaved Family Members.The relationship between cancer patients' place of death and bereaved caregivers' mental health status.Unfinished Business in Families of Terminally Ill With Cancer Patients.Meaningful Communication Before Death, but Not Present at the Time of Death Itself, Is Associated With Better Outcomes on Measures of Depression and Complicated Grief Among Bereaved Family Members of Cancer Patients.Care strategy for death rattle in terminally ill cancer patients and their family members: recommendations from a cross-sectional nationwide survey of bereaved family members' perceptions.Which quality of life instruments are preferred by cancer patients in Japan? Comparison of the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-C30 and the Functional Assessment of Cancer Therapy-General.Care evaluation scale-patient version: measuring the quality of the structure and process of palliative care from the patient's perspective.Prevalence and predictors of conflict in the families of patients with advanced cancer: A nationwide survey of bereaved family members.Changes in Nurses' Knowledge, Difficulties, and Self-reported Practices Toward Palliative Care for Cancer Patients in Japan: An Analysis of Two Nationwide Representative Surveys in 2008 and 2015.Trust in Physicians, Continuity and Coordination of Care, and Quality of Death in Patients with Advanced Cancer.Families' Sense of Abandonment When Patients Are Referred to Hospice.The Japan hospice and palliative evaluation study 4: a cross-sectional questionnaire survey.Palliative care knowledge test for nurses and physicians: validation and cross-cultural adaptationSpecialized palliative care services in Japan: a nationwide survey of resources and utilization by patients with cancer
P50
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P50
description
Forscher
@de
chercheur
@fr
investigador
@es
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
研究者
@zh
name
mitsunori miyashita
@ast
mitsunori miyashita
@en
mitsunori miyashita
@es
mitsunori miyashita
@nl
type
label
mitsunori miyashita
@ast
mitsunori miyashita
@en
mitsunori miyashita
@es
mitsunori miyashita
@nl
prefLabel
mitsunori miyashita
@ast
mitsunori miyashita
@en
mitsunori miyashita
@es
mitsunori miyashita
@nl
P106
P31
P496
0000-0002-7637-0409