A randomised controlled trial of postal versus interviewer administration of a questionnaire measuring satisfaction with, and use of, services received in the year before death.
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Assessing complementary therapy services in a hospice program.Variations in the quality and costs of end-of-life care, preferences and palliative outcomes for cancer patients by place of death: the QUALYCARE study.Inequity in the provision of and access to palliative care for cancer patients. Results from the Italian survey of the dying of cancer (ISDOC).Randomised comparison of three methods of administering a screening questionnaire to elderly people: findings from the MRC trial of the assessment and management of older people in the communityA comparison of strategies to recruit older patients and carers to end-of-life research in primary careCan comprehensive specialised end-of-life care be provided at home? Lessons from a study of an innovative consultant-led community service in the UK.Palliative care for Hindus.Patients' perceptions of palliative care: adaptation of the Quality from the Patient's Perspective instrument for use in palliative care, and description of patients' perceptions of care received.Factors Associated with Participation, Active Refusals and Reasons for Not Taking Part in a Mortality Followback Survey Evaluating End-of-Life Care.No Negative Impact of Palliative Sedation on Relatives' Experience of the Dying Phase and Their Wellbeing after the Patient's Death: An Observational Study.Patients' perceptions of palliative care quality in hospice inpatient care, hospice day care, palliative units in nursing homes, and home care: a cross-sectional study.Development the Care Evaluation Scale Version 2.0: a modified version of a measure for bereaved family members to evaluate the structure and process of palliative care for cancer patientHome care by general practitioners for cancer patients in the last 3 months of life: An epidemiological study of quality and associated factors.Cancer trajectories at the end of life: is there an effect of age and gender?Dying of cancer in Italy: impact on family and caregiver. The Italian Survey of Dying of Cancer.Using a birth cohort to study ageing: representativeness and response rates in the National Survey of Health and Development.A patient and carer survey in a community clinical nurse specialist service.Actual and preferred place of death of cancer patients. Results from the Italian survey of the dying of cancer (ISDOC).How well do current instruments using bereaved relatives' views evaluate care for dying patients?Agent Orange exposure and prevalence of self-reported diseases in Korean Vietnam veteransImportant issues to quality of life among norwegian older adults: an exploratory study.Bereavement needs assessment in specialist palliative care: a review of the literature.A systematic review of instruments related to family caregivers of palliative care patients.Assessing quality of care for the dying: the development and initial validation of a postal self-completion questionnaire for bereaved relatives.The relationship between quality of life and disability across the lifespan for people with spinal cord injury.Approaches to capturing the financial cost of family care-giving within a palliative care context: a systematic review.End-of-life care in residential care homes: a retrospective study of the perspectives of family members using the VOICES questionnaire.Dying for care: the experiences of terminally ill cancer patients in hospital in an inner city health district.Accounts of carers' satisfaction with health care at the end of life: a comparison of first generation black Caribbeans and white patients with advanced disease.What's the diagnosis? Organisational culture and palliative care delivery in residential aged care in New Zealand.The Views of Informal Carers' Evaluation of Services (VOICES): Toward an adaptation for the New Zealand bicultural context.Towards a culturally acceptable end-of-life survey questionnaire: a Bengali translation of VOICES.Community participation for individuals with spinal cord injury living in Queensland, Australia.Palliative care provided by GPs: the carer's viewpoint.Effect of palliative care nurse champions on the quality of dying in the hospital according to bereaved relatives: A controlled before-and-after study.'All the services were excellent. It is when the human element comes in that things go wrong': dissatisfaction with hospital care in the last year of life.Specialist palliative care needs of whole populations: a feasibility study using a novel approach.Bereaved parents' experiences of the use of 'cold bedrooms' following the death of their child.Research sensitivities to palliative care patients."A rewarding conclusion of the relationship": staff members' perspectives on providing bereavement follow-up.
P2860
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P2860
A randomised controlled trial of postal versus interviewer administration of a questionnaire measuring satisfaction with, and use of, services received in the year before death.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
A randomised controlled trial ...... ived in the year before death.
@ast
A randomised controlled trial ...... ived in the year before death.
@en
type
label
A randomised controlled trial ...... ived in the year before death.
@ast
A randomised controlled trial ...... ived in the year before death.
@en
prefLabel
A randomised controlled trial ...... ived in the year before death.
@ast
A randomised controlled trial ...... ived in the year before death.
@en
P2093
P2860
P356
P1476
A randomised controlled trial ...... ived in the year before death.
@en
P2093
Addington-Hall J
McCarthy M
P2860
P304
P356
10.1136/JECH.52.12.802
P577
1998-12-01T00:00:00Z