Published in Int J Palliat Nurs on January 01, 2006
Study protocol: delayed intervention randomised controlled trial within the Medical Research Council (MRC) Framework to assess the effectiveness of a new palliative care service. BMC Palliat Care (2006) 1.07
Presenting evidence-based health information for people with multiple sclerosis: the IN-DEEP project protocol. BMC Med Inform Decis Mak (2012) 0.92
Narratives reflecting the lived experiences of people with brain disorders: common psychosocial difficulties and determinants. PLoS One (2014) 0.90
Unmet needs of patients feeling severely affected by multiple sclerosis in Germany: a qualitative study. J Palliat Med (2014) 0.88
Evidence-based educational guidelines for stroke survivors after discharge home. J Neurosci Nurs (2008) 0.81
Nurses respond to patients' psychosocial needs by dealing, ducking, diverting and deferring: an observational study of a hospice ward. BMC Nurs (2015) 0.75
Dignity in the terminally ill: a cross-sectional, cohort study. Lancet (2002) 3.73
Dignity therapy: a novel psychotherapeutic intervention for patients near the end of life. J Clin Oncol (2005) 3.48
Effect of dignity therapy on distress and end-of-life experience in terminally ill patients: a randomised controlled trial. Lancet Oncol (2011) 2.56
Evidence in palliative care research: How should it be gathered? Med J Aust (2005) 2.09
What do patients receiving palliative care for cancer and their families want to be told? A Canadian and Australian qualitative study. BMJ (2004) 1.94
The patient dignity inventory: a novel way of measuring dignity-related distress in palliative care. J Pain Symptom Manage (2008) 1.56
Exploring the relationship between personal control and the hospital environment. J Clin Nurs (2008) 1.48
Challenging the framework for evidence in palliative care research. Palliat Med (2005) 1.47
Developing guidelines for syringe driver management. Int J Palliat Nurs (2006) 1.38
Desire for hastened death in patients with advanced disease and the evidence base of clinical guidelines: a systematic review. Palliat Med (2006) 1.33
Caregiving for the terminally ill: at what cost? Palliat Med (2005) 1.28
Resistance training and reduction of treatment side effects in prostate cancer patients. Med Sci Sports Exerc (2006) 1.25
Understanding the will to live in patients nearing death. Psychosomatics (2005) 1.21
Meeting the supportive needs of family caregivers in palliative care: challenges for health professionals. J Palliat Med (2004) 1.17
Multivariate methods to identify cancer-related symptom clusters. Res Nurs Health (2009) 1.15
Burden to others and the terminally ill. J Pain Symptom Manage (2007) 1.13
Defining dignity in terminally ill cancer patients: a factor-analytic approach. Psychooncology (2004) 1.13
Supportive and palliative care needs of families of children who die from cancer: an Australian study. Palliat Med (2008) 1.09
Responding to desire to die statements from patients with advanced disease: recommendations for health professionals. Palliat Med (2006) 1.07
Dignity-conserving care: application of research findings to practice. Int J Palliat Nurs (2004) 1.06
Systematic review of the efficacy of antiemetics in the treatment of nausea in patients with far-advanced cancer. Support Care Cancer (2004) 1.05
Learning from dying patients during their final days: life reflections gleaned from dignity therapy. Palliat Med (2010) 1.00
Is it feasible and desirable to collect voluntarily quality and outcome data nationally in palliative oncology care? J Clin Oncol (2008) 0.96
The landscape of distress in the terminally ill. J Pain Symptom Manage (2009) 0.96
Living with Huntington's disease: need for supportive care. Nurs Health Sci (2004) 0.94
Dignity and psychotherapeutic considerations in end-of-life care. J Palliat Care (2004) 0.94
A new approach to eliciting meaning in the context of breast cancer. Cancer Nurs (2003) 0.94
Information needs and preferences of women as they proceed through radiotherapy for breast cancer. Patient Educ Couns (2011) 0.92
Is symptom burden a predictor of anxiety and depression in patients with cancer about to commence chemotherapy? Med J Aust (2009) 0.91
Reliability testing of the FAMCARE-2 scale: measuring family carer satisfaction with palliative care. Palliat Med (2010) 0.91
Emotional care experienced by hospitalised patients: development and testing of a measurement instrument. J Clin Nurs (2008) 0.91
Would people with Parkinson's disease benefit from palliative care? Palliat Med (2006) 0.89
Measuring symptom distress in palliative care: psychometric properties of the Symptom Assessment Scale (SAS). J Palliat Med (2011) 0.89
How do radiation oncology health professionals inform breast cancer patients about the medical and technical aspects of their treatment? Radiother Oncol (2008) 0.88
Risk of suicide in cancer patients in Western Australia, 1981-2002. Med J Aust (2008) 0.86
'If we get too close to your bones they'll go brittle': women's initial fears about radiotherapy for early breast cancer. Psychooncology (2008) 0.86
Schematic representation of case study research designs. J Adv Nurs (2007) 0.85
The prevalence of anxiety and depression in palliative care patients with cancer in Western Australia and New South Wales. Med J Aust (2010) 0.85
Bringing evidence to bear on policy processes: the challenge of the Australian Primary Health Care Research Institute. Med J Aust (2008) 0.84
"But isn't it depressing?" The vitality of palliative care. J Palliat Care (2002) 0.84
A prospective evaluation of Dignity Therapy in advanced cancer patients admitted to palliative care. Palliat Med (2013) 0.84
Education and training in palliative care. Med J Aust (2003) 0.83
Multi-faceted palliative care intervention: aged care nurses' and care assistants' perceptions and experiences. J Adv Nurs (2008) 0.83
Patients' perspectives on the role of radiation therapists. Patient Educ Couns (2007) 0.82
Information needs and coping styles of primary family caregivers of women following breast cancer surgery. Oncol Nurs Forum (2003) 0.82
Ensuring content validity in instrument development: challenges and innovative approaches. Contemp Nurse (2003) 0.82
Development of a pain management programme for family carers of advanced cancer patients. Int J Palliat Nurs (2004) 0.82
Dignity therapy for people with motor neuron disease and their family caregivers: a feasibility study. J Palliat Med (2015) 0.81
Lymphedema Quality of Life Inventory (LyQLI)-Development and investigation of validity and reliability. Qual Life Res (2015) 0.81
Supportive and palliative care needs of families of children with life-threatening illnesses in Western Australia: evidence to guide the development of a palliative care service. Palliat Med (2007) 0.81
Identification of cancer-related symptom clusters: an empirical comparison of exploratory factor analysis methods. J Pain Symptom Manage (2012) 0.80
Undertreatment of nausea and other symptoms in hospitalized cancer patients. Support Care Cancer (2008) 0.80
Predicting family caregiver psychosocial functioning in palliative care. J Palliat Care (2006) 0.80
Palliative care needs of terminally ill people living alone: a service provider perspective. Collegian (2013) 0.80
The impact on sexual functioning of chemotherapy-induced menopause in women with breast cancer. Cancer Nurs (2002) 0.80
Responding to a diagnosis of localized prostate cancer: men's experiences of normal distress during the first 3 postdiagnostic months. Cancer Nurs (2013) 0.79
Cancer-related symptom clusters for symptom management in outpatients after commencing adjuvant chemotherapy, at 6 months, and 12 months. Support Care Cancer (2011) 0.79
Communicating with families of patients in an acute hospital with advanced cancer: problems and strategies identified by nurses. Cancer Nurs (2003) 0.78
Hormone ablation for the treatment of prostate cancer: the lived experience. Urol Nurs (2006) 0.77
Validity and reliability testing of two instruments to measure breast cancer patients' concerns and information needs relating to radiation therapy. Radiat Oncol (2007) 0.77
Testing the feasibility of the Dignity Therapy interview: adaptation for the Danish culture. BMC Palliat Care (2010) 0.77
Comparison of plain ice and flavoured ice for preventing oral mucositis associated with the use of 5 fluorouracil. J Clin Nurs (2005) 0.77
Developing recommendations for implementing the Australian Pain Society's pain management strategies in residential aged care. Australas J Ageing (2008) 0.77
Personality, neuroticism, and coping towards the end of life. J Pain Symptom Manage (2006) 0.77
Measuring symptom distress among frail elders capable of providing self reports. Nurs Health Sci (2005) 0.76
Case study report of two palliative care patients receiving intracerebroventricular (ICV) analgesia. J Palliat Care (2003) 0.76
Evaluating the Navigate Care Model: clinical palliative care pathways based on anticipated care outcomes. Int J Palliat Nurs (2003) 0.75
Investigating euthanasia: methodological, ethical and clinical considerations. Palliat Med (2005) 0.75
Professional relationships in palliative care decision making. Support Care Cancer (2008) 0.75
Mapping the journey: family carers' perceptions of issues related to end-stage care of individuals with muscular dystrophy or motor neurone disease. J Palliat Care (2003) 0.75
Development of a donor driven assessment protocol in Western Australia based on experiences of living renal donors. Nephrol Nurs J (2007) 0.75
Development and testing of a modified version of the brief pain inventory for use in residential aged care facilities. J Am Geriatr Soc (2008) 0.75
Psychometric testing and refinement of the Support Needs Inventory for Parents of Asthmatic Children. J Nurs Meas (2004) 0.75
Content validity and reliability testing of the FIN-PED II: A tool to measure care needs of parents of children with cancer. J Nurs Meas (2006) 0.75
Positioning nursing and midwifery research for the future: external & internal challenges. Collegian (2007) 0.75
Long-term palliative care workers: more than a story of endurance. J Palliat Med (2002) 0.75