262 results on '"van Uden-Kraan, Cornelia F."'
Search Results
2. The use of outcome data in patient consultations from the healthcare professionals’ and patients’ perspectives: A mixed methods study
3. Barriers and facilitators of meaningful patient participation at the collective level in healthcare organizations: A systematic review
4. Shared Decision Making in Health Care Visits for CKD: Patients’ Decisional Role Preferences and Experiences
5. Real-world palbociclib effectiveness in patients with metastatic breast cancer: Focus on neutropenia-related treatment modification strategies and clinical outcomes
6. Development of an online patient decision aid for kidney failure treatment modality decisions
7. Web-based self-help intervention for partners of cancer patients based on acceptance and commitment therapy and self-compassion training: a randomized controlled trial with automated versus personal feedback
8. Cost-utility and cost-effectiveness of a guided self-help head and neck exercise program for patients treated with total laryngectomy: Results of a multi-center randomized controlled trial
9. Evaluation of the Implementation of the Dutch Breast Cancer Surveillance Decision Aid including Personalized Risk Estimates in the SHOUT-BC Study: A Mixed Methods Approach.
10. A nurse-led self-management support intervention for patients and informal caregivers facing incurable cancer: A feasibility study from the perspective of nurses
11. Effectiveness of a guided self-help exercise program tailored to patients treated with total laryngectomy: Results of a multi-center randomized controlled trial
12. Role of eHealth application Oncokompas in supporting self-management of symptoms and health-related quality of life in cancer survivors: a randomised, controlled trial
13. Santeon’s Lessons from a Decade of Implementing Value-Based Health Care
14. The use of outcome data in patient consultations from the healthcare professionals’ and patients’ perspectives: a mixed methods study
15. Introducing Decision Aids into Routine Prostate Cancer Care in The Netherlands: Implementation and Patient Evaluations from the Multi-regional JIPPA Initiative
16. Health-related and cancer-related Internet use by patients treated with total laryngectomy
17. Body changes after cancer: female cancer patients’ perceived social support and their perspective on care
18. Evaluating patient participation in value‐based healthcare: Current state and lessons learned.
19. Patients’ experiences of life review therapy combined with memory specificity training (LRT-MST) targeting cancer patients in palliative care
20. Adoption and implementation of a web-based self-management application “Oncokompas” in routine cancer care: a national pilot study
21. Measuring health-related quality of life in colorectal cancer patients: systematic review of measurement properties of the EORTC QLQ-CR29
22. Development and Evaluation of a Real-World Outcomes-Based Tool to Support Informed Clinical Decision Making in the Palliative Treatment of Patients With Metastatic NSCLC
23. Relations between recurrence risk perceptions and cancer worries in breast cancer survivors.
24. A systematic review of the measurement properties of the Body Image Scale (BIS) in cancer patients
25. Patient-reported physical activity and the association with health-related quality of life in head and neck cancer survivors
26. Supporting Shared Decision-making About Surveillance After Breast Cancer With Personalized Recurrence Risk Calculations: Development of a Patient Decision Aid Using the International Patient Decision AIDS Standards Development Process in Combination With a Mixed Methods Design
27. Neuro-oncology family caregivers’ view on keeping track of care issues using eHealth systems: it’s a question of time
28. Prophylactic exercises among head and neck cancer patients during and after swallowing sparing intensity modulated radiation: adherence and exercise performance levels of a 12-week guided home-based program
29. A guided self-help intervention targeting psychological distress among head and neck cancer and lung cancer patients: motivation to start, experiences and perceived outcomes
30. The need for supportive care among head and neck cancer patients: psychometric assessment of the Dutch version of the Supportive Care Needs Survey Short-Form (SCNS-SF34) and the newly developed head and neck cancer module (SCNS-HNC)
31. Effectiveness and implementation of SHared decision-making supported by OUTcome information among patients with breast cancer, stroke and advanced kidney disease: SHOUT study protocol of multiple interrupted time series
32. Attitudes and preferences toward monitoring symptoms, distress, and quality of life in glioma patients and their informal caregivers
33. An online self-care education program to support patients after total laryngectomy: feasibility and satisfaction
34. Additional file 1 of Development of an online patient decision aid for kidney failure treatment modality decisions
35. Cancer survivors’ perceived need for supportive care and their attitude towards self-management and eHealth
36. A mixed-method study on the generic and ostomy-specific quality of life of cancer and non-cancer ostomy patients
37. Supporting shared decision making about personalised surveillance after breast cancer: the development of a patient decision aid integrating personalised recurrence risk calculations (Preprint)
38. Abstract P4-11-31: Health care professionals’ perspectives on less intensive post-treatment surveillance after breast cancer for women with low risks for recurrences
39. Development of a patient decision aid for the treatment of localised prostate cancer: a participatory design approach
40. Improving access to supportive cancer care through an eHealth application: a qualitative needs assessment among cancer survivors
41. Multimodal Guided Self-Help Exercise Program to Prevent Speech, Swallowing, and Shoulder Problems Among Head and Neck Cancer Patients: A Feasibility Study
42. Health care professionals' perspectives on shared decision making supported by personalised‐risk‐for‐recurrences‐calculations regarding surveillance after breast cancer.
43. Experiences and attitudes of Dutch rheumatologists and oncologists with regard to their patients’ health-related Internet use
44. Meaning-centered group psychotherapy in cancer survivors: a feasibility study
45. O.31.1 - Relations between recurrence risk perceptions and cancer worries in breast cancer survivors.: Presenter(s): Jet Ankersmid, Santeon / University of Twente, Netherlands
46. Determinants of Engagement in Face-to-Face and Online Patient Support Groups
47. Self-Reported Differences in Empowerment Between Lurkers and Posters in Online Patient Support Groups
48. Follow‐up after breast cancer: Variations, best practices, and opportunities for improvement according to health care professionals.
49. Implementation of a decision aid for localized prostate cancer in routine care: A successful implementation strategy
50. Translation of the eHealth Impact Questionnaire for a Population of Dutch Electronic Health Users: Validation Study
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