Julia M. Addington‐hall

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Philosophy

Julia M. Addington‐hall's Degrees

PhD Health Services Research University of Oxford

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Julia M. Addington‐hall's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

The prevalence of symptoms in end-stage renal disease: a systematic review. (2007) (778)
A comparison of the palliative care needs of patients dying from chronic respiratory diseases and lung cancer (2001) (368)
Judging the quality of care at the end of life: can proxies provide reliable information? (2003) (360)
Depression in advanced disease: a systematic review Part 1. Prevalence and case finding (2002) (344)
Who should measure quality of life? (2001) (343)
Dying from cancer: results of a national population-based investigation (1995) (316)
Place of death and access to home care services: are certain patient groups at a disadvantage? (1998) (308)
The healthcare needs of chronic obstructive pulmonary disease patients in the last year of life (2005) (283)
Knowledge and communication difficulties for patients with chronic heart failure: qualitative study (2000) (276)
Symptoms in advanced renal disease: a cross-sectional survey of symptom prevalence in stage 5 chronic kidney disease managed without dialysis. (2007) (251)
Secondary analysis of qualitative data: a valuable method for exploring sensitive issues with an elusive population? (2011) (244)
Place of Death of Older Persons with Dementia. A Study in Five European Countries (2010) (243)
Research sensitivities to palliative care patients. (2002) (236)
THE EXPERIENCE OF DYING WITH DEMENTIA: A RETROSPECTIVE STUDY (1997) (234)
Supporting lay carers in end of life care: current gaps and future priorities (2009) (223)
Which patients with cancer die at home? A study of six European countries using death certificate data. (2010) (203)
The last year of life of COPD: a qualitative study of symptoms and services. (2004) (202)
After-death interviews with surrogates/bereaved family members: some issues of validity. (2001) (199)
How do cancer patients who die at home differ from those who die elsewhere? (1998) (192)
Regional Study of Care for the Dying: methods and sample characteristics (1995) (188)
'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. (2000) (181)
Telephone versus postal surveys of general practitioners: methodological considerations. (1994) (178)
Using satisfaction to measure the quality of palliative care: a review of the literature. (2003) (169)
Specialist palliative care in nonmalignant disease (1998) (169)
Counsellors in English and Welsh general practices: their nature and distribution. (1993) (168)
Population-based study of dying in hospital in six European countries (2008) (166)
Randomised controlled trial of non-directive counselling, cognitive-behaviour therapy, and usual general practitioner care for patients with depression. I: Clinical effectiveness (2000) (162)
Awareness of dying: prevalence, causes and consequences. (1997) (160)
Euthanasia: why people want to die earlier. (1994) (152)
Dying from Heart Disease (1996) (151)
What Facilitates or Impedes Family Communication Following Genetic Testing for Cancer Risk? A Systematic Review and Meta-Synthesis of Primary Qualitative Research (2010) (145)
ABC of palliative care: The carers (1998) (144)
The effect of noninvasive ventilation on ALS patients and their caregivers (2006) (140)
Place of death in the population dying from diseases indicative of palliative care need: a cross-national population-level study in 14 countries (2015) (138)
Extending specialist palliative care to all? (1999) (134)
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. (1998) (121)
A qualitative study of chronic heart failure patients’ understanding of their symptoms and drug therapy (2002) (119)
Research methods in palliative care. (2007) (115)
Spiritual needs in health care (2004) (114)
Depression in advanced disease: a systematic review - Part 1. Prevalence and case finding (2002) (113)
Trajectories of illness in stage 5 chronic kidney disease: a longitudinal study of patient symptoms and concerns in the last year of life. (2011) (110)
Living with and dying from heart failure: the role of palliative care (2002) (109)
Home palliative care for terminal cancer patients: a survey on the final week of life (1999) (109)
End‐Stage Renal Disease: A New Trajectory of Functional Decline in the Last Year of Life (2011) (109)
A randomized controlled trial to evaluate the effectiveness of a brief, behaviorally oriented intervention for cancer‐related fatigue (2007) (108)
Symptoms in the month before death for stage 5 chronic kidney disease patients managed without dialysis. (2010) (107)
International variation in place of death of older people who died from dementia in 14 European and non-European countries. (2015) (106)
Determinants of informal caregivers' satisfaction with services for dying cancer patients. (1996) (105)
The physical and practical problems experienced by cancer survivors: a rapid review and synthesis of the literature. (2011) (104)
Palliative care for non-cancer patients (2001) (100)
Knowledge, ignorance and priorities for research in key areas of cancer survivorship: findings from a scoping review (2011) (96)
Terminal cancer patients and timing of referral to palliative care: a multicenter prospective cohort study. Italian Cooperative Research Group on Palliative Medicine. (1999) (93)
What is important to measure in the last months and weeks of life?: A modified nominal group study. (2006) (91)
Transitions at the end of life for older adults – patient, carer and professional perspectives: a mixed-methods study (2014) (91)
End-of-life issues in acute stroke care: a qualitative study of the experiences and preferences of patients and families (2010) (89)
The value of cognitive interviewing techniques in palliative care research (2007) (88)
Which terminally ill cancer patients receive hospice in-patient care? (1998) (86)
The effectiveness of patient-family carer (couple) intervention for the management of symptoms and other health-related problems in people affected by cancer: a systematic literature search and narrative review. (2012) (86)
Nursing the dying within a generalist caseload: a focus group study of district nurses. (2008) (81)
Which terminally ill cancer patients in the United Kingdom receive care from community specialist palliative care nurses? (2000) (78)
Challenges in transition from intervention to end of life care in intensive care: a qualitative study. (2012) (78)
How people with motor neurone disease talk about living with their illness: a narrative study. (2008) (77)
The experiences of older adults in the community dying from cancer and non-cancer causes: a national survey of bereaved relatives. (2010) (72)
Symptom control, communication with health professionals, and hospital care of stroke patients in the last year of life as reported by surviving family, friends, and officials. (1995) (72)
Educational opportunities in palliative care: what do general practitioners want? (2001) (69)
Attitudes of Danish doctors and nurses to palliative and terminal care (2005) (69)
Depression in palliative care: a systematic review. Part 2. Treatment (2002) (69)
Negotiated dying: a grounded theory of how nurses shape withdrawal of treatment in hospital critical care units. (2011) (68)
End-of-life care and achieving preferences for place of death in England: Results of a population-based survey using the VOICES-SF questionnaire (2014) (68)
Improving district nurses' confidence and knowledge in the principles and practice of palliative care. (2008) (67)
Conflict rationalisation: how family members cope with a diagnosis of brain stem death. (2008) (64)
Palliative care in stroke: a critical review of the literature (2007) (63)
Older adults' experiences of transitions between care settings at the end of life in England: a qualitative interview study. (2012) (62)
Using death certificate data to study place of death in 9 European countries: opportunities and weaknesses (2007) (62)
What does a diagnosis of brain death mean to family members approached about organ donation? A review of the literature. (2008) (61)
The palliative care needs of acute stroke patients: a prospective study of hospital admissions. (2010) (60)
Older adults' attitudes to death, palliative treatment and hospice care (2005) (59)
Euthanasia: the role of good care. (1995) (59)
Participant recruitment in sensitive surveys: a comparative trial of ‘opt in’ versus ‘opt out’ approaches (2013) (58)
The deliverability, acceptability, and perceived effect of the Macmillan approach to weight loss and eating difficulties: a phase II, cluster-randomized, exploratory trial of a psychosocial intervention for weight- and eating-related distress in people with advanced cancer. (2010) (56)
Evaluating palliative care: bereaved family members' evaluations of patients' pain, anxiety and depression. (2004) (56)
Informing future research priorities into the psychological and social problems faced by cancer survivors: a rapid review and synthesis of the literature. (2013) (56)
Perspectives on symptom control in patients receiving community palliative care (2003) (55)
How and why do GPs use specialist palliative care services? (2002) (54)
Variations by age in symptoms and dependency levels experienced by people in the last year of life, as reported by surviving family, friends and officials. (1998) (54)
End-of-life care and preferences for place of death among the oldest old: results of a population-based survey using VOICES-Short Form. (2014) (52)
From 'conductor' to 'second fiddle': older adult care recipients' perspectives on transitions in family caring at hospital admission. (2013) (51)
A research study to identify facilitators and barriers to outcome measure implementation. (2005) (50)
Providing palliative care in primary care: how satisfied are GPs and district nurses with current out-of-hours arrangements? (2000) (49)
Roles, service knowledge and priorities in the provision of palliative care: a postal survey of London GPs (2006) (49)
Symptom management in patients with established renal failure managed without dialysis. (2006) (47)
A national survey of health professionals and volunteers working in voluntary hospice services in the UK. I. Attitudes to current issues affecting hospices and palliative care (2005) (46)
Do home deaths increase distress in bereavement? (2000) (44)
Place of death in metropolitan regions: metropolitan versus non-metropolitan variation in place of death in Belgium, The Netherlands and England. (2010) (44)
Patient descriptions of breathlessness in heart failure. (2005) (43)
Experiences of hospital care reported by bereaved relatives of patients after a stroke: a retrospective survey using the VOICES questionnaire. (2009) (43)
How do Proxies’ Perceptions of Patients’ Pain, Anxiety, and Depression Change during the Bereavement Period? (2004) (42)
Dying at the best time. (1995) (41)
The willingness of palliative care patients to participate in research. (2005) (41)
Quality of life assessment and outcome of palliative care. (2001) (40)
Place of Death and Use of Health Services in the Last Year of Life (2003) (39)
Professionals' views and experiences of using outcome measures in palliative care. (2003) (38)
Do older pedestrians have enough time to cross roads in Dublin ? A critique of the Traffic Management Guidelines based on clinical research findings (2009) (38)
Deaths of children occurring at home in six European countries. (2010) (38)
Physicians' experiences and perspectives regarding the use of continuous sedation until death for cancer patients in the context of psychological and existential suffering at the end of life (2013) (37)
Living into old age with the consequences of breast cancer. (2013) (37)
Palliative care needs to be provided on basis of need rather than diagnosis (1999) (37)
What is different about living alone with cancer in older age? A qualitative study of experiences and preferences for care (2013) (36)
Risk factors for common mental disorder in caregiving and bereavement. (2010) (35)
Older patients' experiences of treatment for colorectal cancer: an analysis of functional status and service use. (2004) (35)
Treatment decisions in older patients with colorectal cancer: the role of age and multidimensional function. (2003) (34)
It just didn't work: the realities of quality assessment in the English health care context. (2004) (34)
Does the ‘Liverpool Care Pathway' facilitate an improvement in quality of care for dying cancer patients? (2013) (33)
The JACS prospective cohort study of newly diagnosed women with breast cancer investigating joint and muscle pain, aches, and stiffness: pain and quality of life after primary surgery and before adjuvant treatment (2014) (33)
The effects of the clinical characteristics of dying cancer patients on informal caregivers' satisfaction with palliative care (1997) (33)
Translating clinical tools in nursing practice. (2003) (32)
A survey of joint and muscle aches, pain, and stiffness comparing women with and without breast cancer. (2013) (31)
Uncertainty and anxiety in the cancer of unknown primary patient journey: a multiperspective qualitative study (2013) (30)
Care of the dying stroke patient in the acute setting (2005) (29)
Developing the methods and questionnaire (VOICES-SF) for a national retrospective mortality follow-back survey of palliative and end-of-life care in England (2017) (27)
depression. I: Clinical effectiveness usual general practitioner care for patients with counselling, cognitive-behaviour therapy, and Randomised controlled trial of non-directive (2006) (25)
Building bridges in palliative care: evaluating a GP Facilitator programme (2003) (25)
What to eat when off treatment and living with involuntary weight loss and cancer: a systematic search and narrative review (2010) (25)
The development of a questionnaire to assess the attitudes of older people to end-of-life issues (AEOLI) (2005) (24)
The Birmingham International Workshop on Supportive, Palliative, and End‐of‐Life Care Research (2006) (24)
Distribution of mental health professionals working on site in English and Welsh general practices. (1993) (23)
The role of counsellors in general practice. A qualitative study. (1996) (23)
Community care for stroke patients in the last year of life: results of a national retrospective survey of surviving family, friends and officials. (1998) (23)
Assessing the quality of care for dying patients from the bereaved relatives' perspective: further validation of "Evaluating care and health outcomes--for the dying". (2014) (22)
VOICES redesign and testing to inform a national end of life care survey (2011) (22)
A national survey of health professionals and volunteers working in voluntary hospices in the UK. II. Staff and volunteers' experiences of working in hospices (2005) (21)
Investigation of whether on-site general practice counsellors have an impact on psychotropic drug prescribing rates and costs. (1996) (20)
A national survey of the provision of support services for people with cancer. (1993) (20)
‘You can't say, “what about me?” I'm not the one with cancer’: information and support needs of relatives (2015) (19)
Palliative Care: perspectives on caring for dying people in London (2005) (19)
A cohort study of the recovery of health and wellbeing following colorectal cancer (CREW study): protocol paper (2012) (19)
Palliative care services in England: a survey of district nurses' views. (2005) (19)
A comparison of strategies to recruit older patients and carers to end-of-life research in primary care (2012) (19)
Towards a culturally acceptable end-of-life survey questionnaire: a Bengali translation of VOICES. (2005) (19)
Carers' health status (1997) (18)
Discontinuity of care at end of life: a qualitative exploration of OOH end of life care (2013) (17)
Non-cancer patients as an under-served group (2012) (17)
Benefits and challenges of collaborative research: lessons from supportive and palliative care (2011) (17)
Outcomes After Unplanned Admission to Hospital in Older People: Ill‐Defined Conditions as Potential Indicators of the Frailty Trajectory (2012) (16)
Which informal carers are most satisfied with services for dying cancer patients (1996) (15)
Language translation of outcome measurement tools: views of health professionals. (2003) (15)
Assessing palliative care outcomes for people with motor neurone disease living at home. (2004) (15)
The Cancer Experiences Research Collaborative (CECo): building research capacity in supportive and palliative care (2006) (13)
Funding health and social services for older people – a qualitative study of care recipients in the last year of life (2012) (13)
Development and initial validation of a new outcome measure for hospice and palliative care: the St Christopher's Index of Patient Priorities (SKIPP) (2013) (13)
Spanish nurses' preparedness to care for hospitalised terminally ill patients and their daily approach to caring. (2012) (13)
Variations in out of hours end of life care provision across primary care organisations in England and Scotland (2013) (11)
Lessons learnt recruiting to a multi-site UK cohort study to explore recovery of health and well-being after colorectal cancer (CREW study) (2013) (11)
ABC of Palliative Care (2006) (11)
What Does a Diagnosis of Brain Death Mean to Family Members Approached about Organ Donation? A Review of the Literature (2008) (10)
Project to improve management of terminal illness: Summary of findings from PROMOTE (2004) (10)
Determining research priorities for cancer survivorship: consultation and evidence review (2009) (10)
Supportive and palliative care research collaboratives in the United Kingdom: an unnatural experiment? (2007) (10)
Survey research: methods of data collection, questionnaire design and piloting (2007) (10)
Can national surveys be funded successfully from local NHS resources? Evidence from the Regional Study of Care for the Dying. (1995) (10)
Dying for care: the experiences of terminally ill cancer patients in hospital in an inner city health district (2000) (9)
An evaluation of research capacity building from the Cancer Experiences Collaborative (2012) (9)
A NATIONAL SURVEY EXPLORING VIEWS AND EXPERIENCE OF HEALTH PROFESSIONALS ABOUT TRANSFERRING PATIENTS FROM CRITICAL CARE HOME TO DIE (2013) (9)
Epidemiology of cancer pain (2004) (9)
What methods do stakeholders prefer for feeding back performance data: a qualitative study in palliative care. (2004) (9)
Who visits mobile UK services providing cancer information and support in the community? (2010) (9)
An evaluation of patient satisfaction with care provided by a multidisciplinary cancer team (1992) (8)
Living and dying from heart failiure: the role of palliative care (2002) (8)
Developing methods to improve the quality of end-of-life care (2004) (8)
The networks of care surrounding cancer palliative care patients (2015) (8)
Project to impROve management of terminal illnEss (PROMOTE). (2001) (8)
The Health and Social Service Needs of Chronic Obstructive Pulmonary Disease (COPD) patients in the last year of life. (2003) (7)
What is the potential for the use of clinical outcome measures to be computerised? Findings from a qualitative research study. (2004) (7)
The legacy of cancer on depression and anxiety. (2013) (6)
Building Bridges in Palliative Care: The Macmillan GP Facilitator Programme: An Evaluation. (2001) (5)
Extending palliative care to chronic conditions (2005) (5)
End Results (2001) (5)
Best practices in research methods: palliative care research in practice (2005) (5)
[Quality of life at the end of life. Analysis of the quality of life of oncologic patients treated with palliative care. Results of a multicenter observational study (staging)]. (1999) (5)
Palliative Care Research in the Face of Uncertainty (2008) (4)
Referral patterns and access to specialist palliative care (2004) (4)
Educational opportunities in palliative care: What do GPs want? (2001) (4)
What are the views and experiences of critical care nurses when involved in providing and facilitating end of life care to patients and families (2009) (4)
Feeding back survey research findings within palliative care. Findings from qualitative research. (2005) (4)
Palliative care patients’ perceptions of the work involved in understanding and managing the network of care provision surrounding them (2015) (4)
Developing a non-cancer service: a resource for hospices (2007) (3)
The Palliative Care Research Society in the UK (2003) (3)
Which patients with cancer die at home in six ageing countries in Europe (2010) (3)
Palliative care research in practice. (2005) (3)
End of life care in intensive care settings: a case study approach to explore decision making and processes. National Institute for Health Research, Research for Patient Benefit Programme PB-PG-0107-12274 (2009) (3)
Palliative care in acute stroke : final report. (2008) (3)
Clinical Pain Management - Cancer Pain (2004) (2)
Euthanasia: why people want to die earlier. (1994) (2)
Life on the list: an exploratory study of the life world of individuals waiting for a kidney transplant (2010) (2)
Care of the dying in Cornwall: a survey of bereaved relatives (2001) (2)
A toolkit for the design and planning of locally-led VOICES end of life care surveys (2011) (2)
Do GP facilitators make a difference in palliative care (2001) (2)
Summary of a national survey of health professionals and volunteers working in voluntary hospices (2001) (2)
Overcoming obstacles to conducting trials in the context of palliative care: An exploratory phase II cluster randomised trial to investigate the effectiveness of the ‘Macmillan Approach to Weight loss and Eating difficulties’ (MAWE) (2009) (2)
What does a diagnosis of brain stem death mean to family members who are approached about organ donation (2008) (2)
What is an appropriate diet for people living with cancer and involuntary weight loss: A systematic review (2010) (1)
‘Many hands make light work’ or ‘too many cooks spoil the broth’? Achieving the tricky balance of appropriate involvement in palliative care for cancer (2012) (1)
'From Conductor to Second Fiddle: Transitions in family caring when community-dwelling older people are admitted to hospital' (2011) (1)
The impact of non-invasive ventilation on quality of life of ALS patients and their carers (2006) (1)
Benefi ts and challenges of collaborative research : lessons from supportive and palliative care (2011) (1)
A guide to VOICES-SC: a version of the VOICES questionnaire developed specifically for hospices and specialist palliative care services (2010) (1)
Survey of joint aches, pains and stiffness in women with primary breast cancer (2008) (1)
What impact did the Department of Health educational and supportive programme for district and community nurses in the principles and practices of palliative care have on nurses' confidence and knowledge? (2006) (1)
JAN Forum: your views and letters (2002) (1)
Is access to community nursing for palliative care patients equitable (2004) (1)
The JACS prospective cohort study of newly diagnosed women with breast cancer investigating joint and muscle pain, aches, and stiffness: pain and quality of life after primary surgery and before adjuvant treatment (2014) (1)
The Experiences of critical care nurses when involved in providing and facilitating end of life patient and family care (2009) (1)
P29 Out of control? Experiences of transitions between care settings at the end of life for older adults with heart failure: a qualitative study (2010) (1)
24-hour district nursing services for palliative care patients: the challenge for cancer networks. (2004) (1)
How do people with cancer and palliative care needs understand and contribute to the management of communication surrounding their care? (2012) (1)
410 INVITED Nurses Attitudes Towards Caring for Dying Patients in Acute Settings (2011) (1)
Supporting relatives : an investigation into obstacles and aids to information exchange within families affected by cancer : interim report. (2009) (1)
Michael Young and Lesley Cullen, A Good Death: Conversations with East Londoners, Routledge, London, 1996, 249 pp., hbk £45.00, ISBN 0 415 13797 7. (1997) (1)
Hospice staff and volunteers: why do they do it and what do they think? (1999) (1)
Clinical challenges in non-malignant disease: overview (2003) (1)
The palliative care needs of COPD patients at the end of life (2004) (1)
Male carers' perceptions of support for adults with multiple sclerosis: national survey findings (2012) (1)
Memory in depression (1988) (0)
Inter-professional relationships: an overlooked influence on end of life transitions for older adults: a qualitative study in England (2013) (0)
Palliative care for heart disease (1997) (0)
Treatment decisions in older patients with colorectal cancer: the role of age and functional status (2001) (0)
Systematic review of research evidence in the UK between 1997 and 2010 on : preferences for place of care and death (2011) (0)
Joint Aches and Quality-of-Life in Breast Cancer Patients (2013) (0)
Response to: Buchan J.E.F., Corner J. & Bond S. (2003) JAN Forum. Journal of Advanced Nursing 43, 531-534. (2003) (0)
Palliative Care in Acute Stroke: Interim Analysis. (2007) (0)
Oxford Textbook of Palliative Medicene - 3rd Edition (2004) (0)
How accurate are GP's estimates of prognosis? (2005) (0)
Providing palliative care at home in the UK: how do family doctors work with specialist services? (2001) (0)
A feasibility study: a mixed methods exploratory phase II cluster randomised trail to investigate the effectiveness of the 'Macmillan Approach to Weight loss and Eating difficulties'(MAWE). (2009) (0)
From conductor to second fiddle: informal caring transitions at older people's hospital admission in the last few months of life (2011) (0)
Health professionals' views on translating clinical tools: an exploratory study with special reference to the Palliative care Outcome Scale (2002) (0)
Analysis of linked Hospital Episode Statistics and mortality data (2014) (0)
How to be a 'good carer'? Perspectives on older adults' end of life care from family carers and health and social care professionals (2012) (0)
Care at home during the last three months of life for people in the South of England following a stroke: views of bereaved relatives (2006) (0)
Out-of-hours care in the last months of life: the needs of cancer and noncancer patients (2004) (0)
Cancer services. Left to chance. (2001) (0)
4224 Exploring the breast cancer experiences, needs and preferences of women aged 70 years and over (2009) (0)
Palliative Care Nursing: Principlaes and Evidence for Practice (2004) (0)
Issues in education provision for new hospice services for non-cancer patients (2007) (0)
How to write a paper (2007) (0)
Manageability of referrals to hospice projects for non-cancer patients (1970) (0)
Management of advanced disease 4th Edition (2004) (0)
Exploring the breast cancer experiences, needs and preferences of women aged 70 years and over: a study in progress (2008) (0)
The last three days of life following a stroke: views of bereaved relatives (2005) (0)
Patient and family experiences of care in the UK : a systematic review of research evidence between 1997 and 2010 on patient and family experiences of information disclosure, communication and decision-making involvement (2011) (0)
Achieving preferred place of care and death: Results from a post bereavement survey (2012) (0)
Background, context and scope (2014) (0)
4160 A survey of joint aches, pains and muscle stiffness comparing women with and without breast cancer (2009) (0)
A study to explore the experiences and support needs of older family caregivers caring for family members (or friends) with cancer (2009) (0)
Authors' response (1999) (0)
Publications and conference presentations (2014) (0)
Plenary: Do people with severe heart failure need palliative care? (2004) (0)
Measurement of subjective symptoms: depression (2005) (0)
Home death for children dying in six European countries (2009) (0)
Assessing cultural acceptability, sensitivity and appropriateness of translated versions of palliative care evalutaions in South Asian communities. (2004) (0)
Acknowledgement to assessors (2014) (0)
Palliative care in Acute Stroke. (2007) (0)
A report on older women’s experience of breast cancer alongside other health conditions (2010) (0)
British Medical Journal (1894) (0)
Identifying how people with MNDIALS talk about living through their illness: A narrative study to enhance self-management (2007) (0)
The effect of psychosocial intervention for cancer patient-carer dyads on symptom experience: a systematic review (2010) (0)
A guide to The St Christopher’s Hospice Patient Priorities Measure (SKIPP) (2010) (0)
How do family doctors want to receive palliative care education and what contribution can specialist services make (2001) (0)
Planning the first national end of life care survey (2012) (0)
Breathlessness in heart failure - the patients' experience (2001) (0)
13th International Symposium on ALS/MND (2002) (0)
Prevalence of depression in chronic heart failure (2001) (0)
Exploring the breast cancer experiences, needs and preferences of women aged 70 years and over. In INVOLVE National Conference: Public Involvement in Research: Getting it Right and Making a Difference, Nottingham, UK, (11-12 November 2008). (2008) (0)
A cohort study of pain in women with primary breast cancer – baseline data (2012) (0)
Male carers' perceptions of support for themselves: findings from a national survey (2012) (0)
ABS56: The last year of life of COPD: the carers’ perspective (2006) (0)
Does palliative care education impact on district nursing confidence (2004) (0)
A comparison of the quality of care provided to cancer patients in the last three months of life in hospices compared to hospitals, from the perspective of bereaved relatives: Results using the VOICESquestionnaire (2006) (0)
A systematic review on nonpharmacological interventions of cancer-related fatigue (2004) (0)
Evaluating a community nurse palliative care educational programme: the views of family doctors (2004) (0)
When randomised controlled trials are not possible - design issues from national evaluation. (2004) (0)
Psychiatric morbidity amongst bereaved relatives of cancer patients: does it make a difference if the cancer patient received specialist palliative care? (1999) (0)
End of life care and preferred place of death for the over 80s: results from a VOICES post-bereavement survey (2012) (0)
Answering our research questions (2014) (0)
Planning the first English end of life care survey (2012) (0)
An in-depth investigation of the experience ofuncertainty in cancer of unknown primary (2013) (0)
Postal questionnaires to bereaved carers - are they still feasible and ethical in England? (2004) (0)
The VOICES-SF: a new questionnaire to measure bereaved family members' experience of palliative and end of life care (2010) (0)
P27 Older adults with cancer—are those who live alone at the end of life a disadvantaged group? A qualitative study (2010) (0)
Best Practices in Reasearch Methods/Les meilleures pratiques en matiére de méthodes de recherche - Palliative Care Research in Practice (2005) (0)
Cancer Experiences Research Collaborative Annual Progress Report, year 2: May 2007-April 2008. (2007) (0)
Palliative care in acute stroke: preliminary analysis. (2007) (0)
The Cancer Experiences Collaborative (CECo) UK for the development of research capacity in supportive and palliative care: Narratives of cancer and life-limiting illness (2007) (0)
A longitudinal cohort of 578 women diagnosed with primary breast cancer across the south of England and Wales (2013) (0)
Left to chance. inequitable distribution of cancer, mortality and access to services (2001) (0)
Outcomes following unplanned admission to hospital in older people admitted for rehabilitation? Findings from the Southampton Grip Strength Study (2012) (0)
A randomised comparative trial of recruitment approach in a population-based post-bereavement survey using the VOICES-SF questionnaire (2010) (0)
Aches and quality-of-life in breast cancer patients (2013) (0)
The last year of chronic obstructive pulmonary disease; a questionnaire survey (2002) (0)
1105 Older patients' experiences of colorectal cancer: functional status and service use following treatment (2003) (0)
What affects community nurses' discussion of diagnosis and prognosis with dying patients? (2001) (0)
Retrospective versus prospective studies of the last year of life (1998) (0)
The provision of palliative care within primary care in London: Final report of a research and development project across five PCTs. (2005) (0)

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Julia M. Addington‐hall's Published Works

Published Works

Julia M. Addington‐hall's AcademicInfluence.com Rankings