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Table 2 Delay information for Window trials location in consent compared to patient preference

From: Improving oncology first-in-human and Window of opportunity informed consent forms through participant feedback

 

Key concepts

Purpose

Trial schedule

Beginning of risks section

End of risks section

Location of delay information in consent forms (n = 5)

20% (1)

40% (2)

0

0

40% (2)

Participant preferences for location of delay information (n = 17)

18% (3)

29% (5)

6% (1)

18% (3)

24% (4)

  1. One Windows participant had no preference