Talking with terminally ill patients and their caregivers about death, dying, and bereavement: is it stressful? Is it helpful?
about
Ethical and logistical considerations of multicenter parental bereavement researchThe attitudes of brain cancer patients and their caregivers towards death and dying: a qualitative studyIs the qualitative research interview an acceptable medium for research with palliative care patients and carers?Measuring Family Members' Satisfaction with End-of-Life Care in Long-Term Care: Adaptation of the CANHELP Lite Questionnaire.Communication with relatives and collusion in palliative care: a cross-cultural perspectiveSubject Recruitment and Retention against Quadruple Challenges in an Intervention Trial of End-of-Life CommunicationPatient, caregiver, health professional and researcher views and experiences of participating in research at the end of life: a critical interpretive synthesis of the literature.Parents' views of involvement in concurrent research with their neonates.Death talk: gender differences in talking about one's own impending deathConducting research interviews with bereaved family carers: when do we ask?The effect of caregiving on bereavement outcome: study protocol for a longitudinal, prospective study.Tailoring traditional interviewing techniques for qualitative research with seriously ill patients about the end-of-life: a primer.End-of-life care research with bereaved informal caregivers--analysis of recruitment strategy and participation rate from a multi-centre validation studyDo oncologists engage in bereavement practices? A survey of the Israeli Society of Clinical Oncology and Radiation Therapy (ISCORT).Research participation experiences of parents of children with cancer who were asked about their child's prognosisFactors Associated with Participation, Active Refusals and Reasons for Not Taking Part in a Mortality Followback Survey Evaluating End-of-Life Care.Future chiropractic physicians: toward a synthesis of select concepts in the behavioral sciences in health care and the society-culture-personality model for the 21st century.Chiropractic physicians: toward a select conceptual understanding of bureaucratic structures and functions in the health care institutionProtocol for the End-of-Life Social Action Study (ELSA): a randomised wait-list controlled trial and embedded qualitative case study evaluation assessing the causal impact of social action befriending services on end of life experiencePrehypertension and risk of cardiovascular disease.Survey burden for family members surveyed about end-of-life care in the intensive care unit.Is Participating in Psychological Research a Benefit, Burden, or Both for Medically Ill Youth and Their Caregivers?.When silence is not golden: Engaging adolescents and young adults in discussions around end-of-life care choices.Religion, spirituality, and health: the research and clinical implicationsBurden and benefit of psychosocial research at the end of lifePeaceful surrender to death without futile bargaining to live relieves terminal air hunger and anguish.Researching breathlessness in palliative care: consensus statement of the National Cancer Research Institute Palliative Care Breathlessness Subgroup.Opening end-of-life discussions: how to introduce Voicing My CHOiCES™, an advance care planning guide for adolescents and young adults.Interference Between Family Caregivers' Mental Disorders and Their Estimates of Quality of Dying and Death (QODD) of Their Loved Ones.Communication in palliative care: talking about the end of life, before the end of life.The psychosocial needs of students conducting research with patients and their families in advanced cancer and palliative care: A scoping review.Advance medical directives: a proposed new approach and terminology from an Islamic perspective.The views of patients with advanced cancer regarding participation in serial questionnaire studies.Human papilloma virus (HPV) status, p16INK4a, and p53 overexpression in epithelial malignant and borderline ovarian neoplasms.A feasibility study of a two-session home-based cognitive behavioral therapy-insomnia intervention for bereaved family caregivers.Approaches to death and dying: a cultural comparison of Turkey and the United States.Psychometric evaluation of the Persian version of the Templer's Death Anxiety Scale in cancer patients.End-of-Life Care: Consensus Statement by Indian Academy of Pediatrics.Goals set in the land of the living/dying: a longitudinal study of patients living with advanced cancer.Terminal delirium misdiagnosed as major psychiatric disorder: Palliative care in a psychiatric inpatient unit.
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P2860
Talking with terminally ill patients and their caregivers about death, dying, and bereavement: is it stressful? Is it helpful?
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Talking with terminally ill pa ...... s it stressful? Is it helpful?
@ast
Talking with terminally ill pa ...... s it stressful? Is it helpful?
@en
type
label
Talking with terminally ill pa ...... s it stressful? Is it helpful?
@ast
Talking with terminally ill pa ...... s it stressful? Is it helpful?
@en
prefLabel
Talking with terminally ill pa ...... s it stressful? Is it helpful?
@ast
Talking with terminally ill pa ...... s it stressful? Is it helpful?
@en
P2093
P1476
Talking with terminally ill pa ...... s it stressful? Is it helpful?
@en
P2093
Diane L Fairclough
Linda L Emanuel
P304
P356
10.1001/ARCHINTE.164.18.1999
P407
P577
2004-10-01T00:00:00Z