"This graft-vs.-host disease determines my life. That's it."-A qualitative analysis of the experiences and needs of allogenic hematopoietic stem cells transplantation survivors in Germany
A discrete choice experiment to assess cancer patients' preferences for when and how to make treatment decisions
A qualitative study on patients' and their support persons' preferences for receiving one longer consultation or two shorter consultations when being informed about allogeneic hematopoietic stem cell transplantation
Australian GPs' perceptions of barriers and enablers to best practice palliative care: a qualitative study
Exploring health literacy and preferences for risk communication among medical oncology patients
Exploring women's experiences with a decision aid for neoadjuvant systemic therapy for operable breast cancer
General practitioners' perceptions of best practice care at the end of life: a qualitative study.
Not asking cancer patients about their preferences does make a difference. A cross-sectional study examining cancer patients' preferred and perceived role in decision-making regarding their last important cancer treatment
Not having adequate time to make a treatment decision can impact on cancer patients' care experience: results of a cross-sectional study
Support persons' preferences for the type of consultation and the format of information provided when making a cancer treatment decision
Systematic review of barriers and enablers to the delivery of palliative care by primary care practitioners
Wilfully out of sight? A literature review on the effectiveness of cancer-related decision aids and implementation strategies
Women's experiences with deciding on neoadjuvant systemic therapy for operable breast cancer: a qualitative study
Working towards patient-centred decision making in cancer care
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