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What experience, if any, have you had involving the public or patients in your research?
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Describe your experiences of leading/implementing a study that includes the patients, public or partnering organizations within a research study
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What parts of the research were they involved in?
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What are your opinions or views on how patient engagement works in research?
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Based on your experience, what are the downsides to involving patients in research
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What do you think about the prospect of involving patients in the mySupport study?
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What do you think about involving care partners in the study?
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What do you think about involving partner organizations in this study such as the Alzheimer's Society?
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How prepared do you feel to work with patients and care partners on this project
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What kind of training do you think would be helpful for this?
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Thinking about the mySupport study, do you think there will be barriers related to patient engagement within this project
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What is your opinion related to working with different countries in this project?