about
The Carer Support Needs Assessment Tool (CSNAT) for use in palliative and end-of-life care at home: a validation study.Recommendations for managing missing data, attrition and response shift in palliative and end-of-life care research: part of the MORECare research method guidance on statistical issues.A comparison of strategies to recruit older patients and carers to end-of-life research in primary careWhat is different about living alone with cancer in older age? A qualitative study of experiences and preferences for care.Evaluating complex interventions in end of life care: the MORECare statement on good practice generated by a synthesis of transparent expert consultations and systematic reviews.The impact of the carer support needs assessment tool (CSNAT) in community palliative care using a stepped wedge cluster trial.Prediction of appropriate timing of palliative care for older adults with non-malignant life-threatening disease: a systematic review.Barriers to effective communication across the primary/secondary interface: examples from the ovarian cancer patient journey (a qualitative study).The selection and use of outcome measures in palliative and end-of-life care research: the MORECare International Consensus Workshop.Mixed methods research in the development and evaluation of complex interventions in palliative and end-of-life care: report on the MORECare consensus exercise.Supporting lay carers in end of life care: current gaps and future priorities.A systematic review of instruments related to family caregivers of palliative care patients.MORECare research methods guidance development: recommendations for ethical issues in palliative and end-of-life care research.An evaluation of research capacity building from the Cancer Experiences Collaborative.A revised model for coping with advanced cancer. Mapping concepts from a longitudinal qualitative study of patients and carers coping with advanced cancer onto Folkman and Greer's theoretical model of appraisal and coping.Benefits and challenges of collaborative research: lessons from supportive and palliative care.Exploring differences in referrals to a hospice at home service in two socio-economically distinct areas of Manchester, UK.Enabling a family caregiver-led assessment of support needs in home-based palliative care: Potential translation into practice.Supporting family caregivers to identify their own needs in end-of-life care: Qualitative findings from a stepped wedge cluster trial.Controlling cancer pain in primary care: the prescribing habits and knowledge base of general practitioners.Breaking bad news about transitions to dying: a qualitative exploration of the role of the District Nurse.Quality of life measures (EORTC QLQ-C30 and SF-36) as predictors of survival in palliative colorectal and lung cancer patients.Improving communication with palliative care cancer patients at home - A pilot study of SAGE & THYME communication skills model.School children's own views, roles and contribution to choices regarding diet and activity in Spain.Predicting cancer patients' participation in support groups: a longitudinal study.General practitioners' and district nurses' views of hospital at home for palliative care.The influence of patient and carer age in access to palliative care services.Informal carer bereavement outcome: relation to quality of end of life support and achievement of preferred place of death.Place of death and access to home care services: are certain patient groups at a disadvantage?How do patients who participate in cancer support groups differ from those who do not?Caring for the dying: how well prepared are general practitioners? A questionnaire study in Wales.Who cares for the carers at hospital discharge at the end of life? A qualitative study of current practice in discharge planning and the potential value of using The Carer Support Needs Assessment Tool (CSNAT) Approach.Funding health and social services for older people - a qualitative study of care recipients in the last year of life.Defining patients as palliative: hospital doctors' versus general practitioners' perceptionsResilience for family carers of advanced cancer patients—how can health care providers contribute? A qualitative interview study with carersPsychological morbidity and general health among family caregivers during end-of-life cancer care: A retrospective census surveyADAPTATION, FACE AND CONTENT VALIDATION OF A PALLIATIVE CARE NEEDS ASSESSMENT TOOL FOR PEOPLE WITH INTERSTITIAL LUNG DISEASEDevelopment of a Carer Support Needs Assessment Tool (CSNAT) for end-of-life care practice at home: A qualitative studyThe need for new perspectives on evaluation of palliative careParents’ contrasting views on diet versus activity of children: Implications for health promotion and obesity prevention
P50
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P50
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Gunn Grande
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A-6163-2011
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P1153
7003738840
P21
P31
P3829
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0000-0003-2200-1680
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2000-01-01T00:00:00Z