505 results on '"JURASKOVA, ILONA"'
Search Results
2. An online intervention to improve oncology health professional self-efficacy in communicating with carers: Hybrid effectiveness-implementation evaluation of the eTRIO program
3. Stakeholder perspectives on the impact of COVID-19 on oncology services: a qualitative study
4. Preferences for return of germline genome sequencing results for cancer patients and their genetic relatives in a research setting
5. Empowering family carers of people with multimorbidity as partners in chronic health care: Insights from health professionals
6. Psychometric assessment of the Concerns about Late Effects in Oncology Questionnaire (CLEO) among female breast cancer survivors
7. Stakeholder perspectives of system-related errors: Types, contributing factors, and consequences
8. Psychological impact of comprehensive tumor genomic profiling results for advanced cancer patients
9. Psychological predictors of cancer patients' and their relatives’ attitudes towards the return of genomic sequencing results
10. Measuring female breast cancer survivors’ concerns about late effects of treatment: initial development of the Concerns about Late Effects in Oncology Questionnaire (CLEO)
11. Cancer patient knowledge about and behavioral intentions after germline genome sequencing
12. Fear of cancer recurrence in patients undergoing germline genome sequencing
13. The emotional impact of COVID-19 on Australian cancer patients, their caregivers, and oncology health professionals over time: a longitudinal qualitative study
14. Improving breast cancer nurses’ management of challenging situations involving family carers: Pilot evaluation of a brief targeted online education module (TRIO-Conflict)
15. The impact of management option on out-of-pocket costs and perceived financial burden among men with localised prostate cancer in Australia within 6 months of diagnosis
16. Fifteen year quality of life outcomes in men with localised prostate cancer : population based Australian prospective study
17. Considering the type and timing of breast reconstruction after mastectomy: Qualitative insights into women's decision-making
18. Medication errors related to computerized provider order entry systems in hospitals and how they change over time: A narrative review
19. Family communication about genomic sequencing: A qualitative study with cancer patients and relatives
20. Co-designing an online treatment decision aid for men with low-risk prostate cancer: Navigate
21. Online resources for family caregivers of cognitively competent patients: A review of user-driven reputable health website content on caregiver communication with health professionals
22. Improving the wellbeing of people with advanced cancer and their family carers: protocol for an effectiveness-implementation trial of a dyadic digital health intervention (FOCUSau) (Preprint)
23. Correction to: Navigate: a study protocol for a randomised controlled trial of an online treatment decision aid for men with low-risk prostate cancer and their partners
24. Navigate: a study protocol for a randomised controlled trial of an online treatment decision aid for men with low-risk prostate cancer and their partners
25. Phase II Randomised Controlled Trial of a patient decision-aid website to improve treatment decision-making for young adults with bipolar II disorder: A feasibility study protocol
26. An Analysis of Incident Reports Related to Electronic Medication Management: How They Change Over Time.
27. Co‐designing an online treatment decision aid for men with low‐risk prostate cancer: Navigate
28. Principles of Treatment of Sexual Dysfunction
29. Managing challenging interactions with family caregivers in the cancer setting: Guidelines for clinicians (TRIO Guidelines-2)
30. Facilitating collaborative and effective family involvement in the cancer setting: Guidelines for clinicians (TRIO Guidelines-1)
31. A systematic review of women’s satisfaction and regret following risk-reducing mastectomy
32. The TRIO Framework: Conceptual insights into family caregiver involvement and influence throughout cancer treatment decision-making
33. Development of online education modules to improve carer engagement in cancer care: Design and user experience evaluation of the eTRIO modules for clinicians, patients and carers (Preprint)
34. A randomised controlled trial evaluating the utility of a patient Decision Aid to improve clinical trial (RAVES 08.03) related decision-making
35. An exploration of Australian psychologists' role in assessing women considering risk-reducing or contralateral prophylactic mastectomy
36. Improving treatment decision-making in bipolar II disorder: a phase II randomised controlled trial of an online patient decision-aid
37. A new grounded theory model of sexual adjustment to HIV: facilitators of sexual adjustment and recommendations for clinical practice
38. Stakeholder perspectives on the impact of Covid-19 on Oncology services: A qualitative study
39. What is the optimal tool for measuring abortion stigma? A systematic review
40. Communication and decision-making in mental health: A systematic review focusing on Bipolar disorder
41. Family involvement in cancer treatment decision-making: A qualitative study of patient, family, and clinician attitudes and experiences
42. Knowledge, attitudes and decision-making preferences of men considering participation in the TROG RAVES Prostate Cancer Trial (TROG 08.03)
43. Adjustment and Coping Mechanisms for Individuals with Genetic Aortic Disorders
44. Positive relations between sexual quality of life and satisfaction with healthcare in women living with HIV and/or HCV: Results from a multicountry study
45. Psychological Distress Mediates the Relationship Between Pain and Disability in Hand or Wrist Fractures
46. A Qualitative Exploration of Clinician Views and Experiences of Treatment Decision-Making in Bipolar II Disorder
47. Women with gynaecological cancer awaiting radiotherapy: Self-reported wellbeing, general psychological distress, symptom distress, sexual function, and supportive care needs
48. The PiGeOn project: protocol of a longitudinal study examining psychosocial and ethical issues and outcomes in germline genomic sequencing for cancer
49. The PiGeOn project: protocol for a longitudinal study examining psychosocial, behavioural and ethical issues and outcomes in cancer tumour genomic profiling
50. Attitudes and experiences of family involvement in cancer consultations: a qualitative exploration of patient and family member perspectives
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