Patient perspectives on re-consenting for each new study. Likert scale responses of leukemia patients’ perceptions on re-consent was quantified. Question: How would you feel if you had to give permission to use your stored biological sample and health information before each new study? (a) I would feel it was a waste of time and money. (b) I would feel bothered. (c) I would feel I have control. (d) I would feel more trust in the study. (e) I would feel respected and involved. * indicates the questions to which patient responses were statistically significant. Due to rounding, totals may not equal 100%.
Master et al. BMC Medical Genomics 2013 6:8 doi:10.1186/1755-8794-6-8