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Palliative Medicine|June 13, 2019
Which outcome domains are important in palliative care and when? An international expert consensus workshop, using the nominal group techniqueSusanne de Wolf-Linder, Marsha Dawkins, Francesca Wicks, et al.
Research Involvement and Engagement|February 8, 2024
A framework for more equitable, diverse, and inclusive Patient and Public Involvement for palliative care researchSarah Mitchell, Nicola Turner, Kate Fryer, et al.
European Journal of Public Health|November 28, 2018
Factors associated with older people's emergency department attendance towards the end of life: a systematic reviewAnna E Bone, Catherine J Evans, Simon N Etkind, et al.
Research Involvement and Engagement|July 3, 2025
Evaluation of the impact of patient and public involvement on doctoral students in palliative dementia care researchWoo Suk Yang, Joshua Rothwell, Matthew Severyn, et al.
BMC Medicine|February 28, 2016
Measures to assess commonly experienced symptoms for people with dementia in long-term care settings: a systematic reviewClare Ellis-Smith, Catherine J Evans, Anna E Bone, et al.
The Cochrane Database of Systematic Reviews|September 30, 2020
The effectiveness and cost-effectiveness of hospital-based specialist palliative care for adults with advanced illness and their caregiversSabrina Bajwah, Adejoke O Oluyase, Deokhee Yi, et al.
Journal of Pain and Symptom Management|May 1, 2013
The selection and use of outcome measures in palliative and end-of-life care research: the MORECare International Consensus WorkshopCatherine J Evans, Hamid Benalia, Nancy J Preston, et al.
Journal of Medical Internet Research|August 16, 2024
Factors Influencing the Implementation of Digital Advance Care Planning: Qualitative Interview StudyAndy Bradshaw, Jacqueline Birtwistle, Catherine J Evans, et al.
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