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How can trials make better use of routine clinical care and/or existing data collection to improve retention?
- “How can we encourage trialists to use routine data linkage more in measuring outcomes so as to reduce patient burden during follow up?” (Frontline staff or other staff involved or invested in trial retention (e.g. Research Nurse, Trial Manager, regulatory or oversight role such as Sponsor or Research Director))
- “Integrate into routine care as much as possible. I am running a trial with close to 2000 patients and no data is collected additional to that in routine care.” (Investigator (e.g. Chief Investigator, Principal Investigator, Co-investigator))
