Project Launch: May 2022
This project aims to develop our understanding of information and shared decision making in myeloma. The project will examine, from a patient perspective: What do health care professionals need to know? How do patients with myeloma and their families want to be involved in treatment decision making? What would help? What is working? Are there any examples of good practice which could be modelled and disseminated across Europe?
This study will work over two phases:
Phase one: qualitative interviews with patients and caregivers to examine positive and best practice experiences in decision making. Findings from this phase will inform a qualitative survey on decision making.
Phase two: short quantitative survey on shared decision making. Survey questions will be developed as themes emerge from the first phase qualitative data.
The outputs of this project will advance and expand our understanding of shared decision-making in practice and provide a set of recommendations for best practices in shared decision-making from a patient perspective.
This project will be managed by MPE and conducted by KU Leuven and Amen.
Recruitment status: Predicted to begin July-August
If you would like to participate in this research, please email firstname.lastname@example.org and we will be in touch on whether you meet the eligibility criteria.