415 results on '"Hasson, Felicity"'
Search Results
2. It Is Changed beyond All Recognition: Exploring the Evolving Habitus of Assistants in Special Schools
3. Data Measurement, Instruments and Sampling.
4. Quantitative Research Designs, Hierarchy of Evidence and Validity.
5. Parents’ experiences of initiation of paediatric advance care planning discussions: a qualitative study
6. The impact of covid-19 on out-of-hours adult hospice care: an online survey
7. Simulated Based Dementia Training: Impact on Empathic Understanding and Behaviour Among Professionals and Carers
8. Trainee district nurses' understanding and perceptions of the palliative care key worker role: a qualitative study.
9. Resilience, stress, and psychological well-being in nursing students: A systematic review
10. 21 Wellbeing of lone working Healthcare Assistants and its impact on staff retention in hospice care at home services
11. Protocol for a mixed methods exploratory investigation into the role and contribution of the healthcare assistant in out-of-hours palliative care
12. Examining public knowledge, attitudes and perceptions towards palliative care: a mixed method sequential study
13. Challenges for palliative care day services: a focus group study
14. Young adults understanding and readiness to engage with palliative care: extending the reach of palliative care through a public health approach: a qualitative study
15. Student nurses' perceptions of the role of the healthcare assistant and the influence of assistants on students clinical learning
16. An evaluation of the reablement service programme on physical ability, care needs and care plan packages
17. Pre-registration nursing student's quality of practice learning: Clinical learning environment inventory (actual) questionnaire
18. International palliative care research priorities: A systematic review
19. An exploration of the views of staff on cultural aspects of end-of-life care in Japanese long-term care facilities: a qualitative study.
20. ‘That just doesn’t feel right at times’ – lone working practices, support and educational needs of newly employed Healthcare Assistants providing 24/7 palliative care in the community: A qualitative interview study
21. The experience of shared decision‐making for patients with end‐stage kidney disease undergoing haemodialysis and their families—A scoping review
22. Implementing Palliative Care Teams Specialized in Dementia in Two Countries: Experiences of Failure and Success
23. Examining constipation assessment and management of patients with advanced cancer receiving specialist palliative care: a multi-site retrospective case note review of clinical practice
24. Out-of-hours community palliative care: a national survey of hospice providers
25. Chinese Diaspora Communities’ Knowledge of and Engagement with Advance Care Planning: A Systematic Integrative Review
26. Implementing Palliative Care Teams Specialized in Dementia in Two Countries: Experiences of Failure and Success
27. sj-pdf-1-pmj-10.1177_02692163231175990 – Supplemental material for ‘That just doesn’t feel right at times’ – lone working practices, support and educational needs of newly employed Healthcare Assistants providing 24/7 palliative care in the community: A qualitative interview study
28. Shared decision-making at the end of life: A focus group study exploring the perceptions and experiences of multi-disciplinary healthcare professionals working in the home setting
29. Research Priorities for the Therapy Professions in Northern Ireland and the Republic of Ireland : A Comparison of Findings from a Delphi Consultation
30. Examining palliative and end of life care research in Ireland within a global context: a systematic mapping review of the evidence
31. Evaluating a partnership model of hospice enabled dementia care: A three-phased monitoring, focus group and interview study
32. Roles and responsibilities of the community palliative care key worker: a scoping review
33. A qualitative study exploring the impact of student nurses working part time as a health care assistant
34. Delegating and supervising unregistered professionals: The student nurse experience
35. What Do Social Workers Think about the Palliative Care Needs of People with Parkinson's Disease?
36. Nursing home managerʼs knowledge, attitudes and beliefs about advance care planning for people with dementia in long‐term care settings: a cross‐sectional survey
37. An exploration of the views of staff on cultural aspects of end-of-life care in Japanese long-term care facilities: a qualitative study
38. sj-pdf-2-pmj-10.1177_02692163221116763 – Supplemental material for Evaluating a partnership model of hospice enabled dementia care: A three-phased monitoring, focus group and interview study
39. sj-pdf-1-pmj-10.1177_02692163221116763 – Supplemental material for Evaluating a partnership model of hospice enabled dementia care: A three-phased monitoring, focus group and interview study
40. Additional file 1 of The impact of covid-19 on out-of-hours adult hospice care: an online survey
41. Additional file 2 of The impact of covid-19 on out-of-hours adult hospice care: an online survey
42. Additional file 3 of The impact of covid-19 on out-of-hours adult hospice care: an online survey
43. Enhancing rigour in the Delphi technique research
44. Palliative care in Japanese long-term care facilities
45. Development and Psychometric Test of the ‘Empathy and Understanding in the Dementia Index’ for Health Professionals
46. Initiation of Paediatric Advance Care Planning Questionnaire
47. 4 Healthcare assistant role in advance care planning discussion: a qualitative study informed by the theory of planned behaviour
48. Pre-loss grief experiences of adults when someone important to them is at end-of-life: A qualitative systematic review.
49. Initiation of Paediatric Advance Care Planning: Cross Sectional Survey of Health professionals reported behaviour
50. Parents’ experiences of initiation of paediatric advance care planning discussions: a qualitative study
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