64 results on '"Hogden, Anne"'
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2. Enablers and barriers to delivering a motor neurone disease multidisciplinary clinic in regional New South Wales, Australia
3. Public Policy in MND Care: The Australian Perspective
4. The complexity of multidisciplinary respiratory care in amyotrophic lateral sclerosis
5. Public health agencies’ use of social media for communication during pandemics: a scoping review of the literature
6. Looking Back, Looking Forward: A Study Protocol for a Mixed-Methods Multiple-Case Study to Examine Improvement Sustainability of Large-Scale Initiatives in Tertiary Hospitals
7. Schema Analysis of Qualitative Data: A Team-Based Approach
8. 20 Co-production and pilot testing a web-based decision aid to support people with motor neurone disease considering a gastrostomy tube (DiAMoND Study)
9. Implementing health system improvement: resources and strategies for interprofessional teams
10. Schema Analysis of Qualitative Data: A Team-Based Approach
11. Disseminating from the Centre to the Frontline: The Diffusion and Local Ownership of a National Health Policy Through the Use of Icons
12. How Does an Accreditation Programme in Residential Aged Care Inform the Way Residents Manage Their Healthcare and Lifestyle?
13. Sustaining improvement of hospital-wide initiative for patient safety and quality: a systematic scoping review
14. Exploring the impact of employee engagement and patient safety
15. Motivational Interviewing to Promote Self-Management
16. MiNDAUS partnership: a roadmap for the cure and management of motor Neurone disease
17. Dimensions of safety culture: a systematic review of quantitative, qualitative and mixed methods for assessing safety culture in hospitals
18. Ward rounds: opportunities for integrating person-centred care.
19. What supports interdisciplinary teamwork during ward rounds to deliver person-centred care?
20. Why and how the work of Motor Neurone Disease Associations matters before and during bereavement: a consumer perspective
21. Who cares for the bereaved? A national survey of family caregivers of people with motor neurone disease
22. Improving knowledge translation for increased engagement and impact in healthcare
23. Grief, depression, and anxiety in bereaved caregivers of people with motor neurone disease: a population-based national study
24. Exploring interdisciplinary teamwork to support effective ward rounds
25. How can we improve patient-centered care of motor neuron disease?
26. Gastrostomy uptake in motor neurone disease: a mixed-methods study of patients’ decision making
27. How Do Interprofessional Healthcare Teams Perceive the Benefits and Challenges of Interdisciplinary Ward Rounds
28. Developing a web-based patient decision aid for gastrostomy in motor neuron disease: a study protocol
29. Clinicians' perceptions of rounding processes and effectiveness of clinical communication
30. Patients, health professionals, and the health system: influencers on patients’ participation in ward rounds
31. Advancing interprofessional theory: Deliberative democracy as a participatory research antidote to power differentials in aged care
32. Appraising risk in active surveillance of localized prostate cancer
33. Fit for purpose? OrganisationaL prOdUctivity and woRkforce wellbeIng in workSpaces in Hospital (FLOURISH): a multimethod qualitative study protocol
34. Comprehensive Researcher Achievement Model (CRAM): a framework for measuring researcher achievement, impact and influence derived from a systematic literature review of metrics and models
35. Relational autonomy in breast diseases care: a qualitative study of contextual and social conditions of patients’ capacity for decision-making
36. The burden of apathy for caregivers of patients with amyotrophic lateral sclerosis
37. Patients’ perspectives of multidisciplinary home-based e-Health service delivery for motor neurone disease
38. Palliative Care in Neurology: Integrating a Palliative Approach to Amyotrophic Lateral Sclerosis Care
39. “Until there is a cure, there is care”: A person-centered approach to supporting the wellbeing of people with Motor Neurone Disease and their family carers
40. Patient-centered decision making in amyotrophic lateral sclerosis: where are we?
41. Communicating risk in active surveillance of localised prostate cancer: a protocol for a qualitative study
42. Women’s Perceptions of Journeying Toward an Unknown Future With Breast Cancer: The “Lives at Risk Study”
43. Understanding stakeholders’ perspectives and experiences of general practice accreditation
44. How does accreditation influence staff perceptions of quality in residential aged care?
45. Faculty Opinions recommendation of From isolation and dependence to autonomy - expectations before and experiences after cochlear implantation in adult cochlear implant users and their significant others.
46. Amyotrophic lateral sclerosis: improving care with a multidisciplinary approach
47. The struggle of translating science into action: Foundational concepts of implementation science
48. Faculty Opinions recommendation of A patient in the clinic; a person in the world. Why shared decision making needs to center on the person rather than the medical encounter.
49. Faculty Opinions recommendation of Six 'biases' against patients and carers in evidence-based medicine.
50. Faculty Opinions recommendation of Hindsight is 20/20: Lessons learned after implementing experience based design.
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