Adding Informed Consent to Other Parts of Your Study

ProofPilot requires all studies to include an Initial Informed Consent immediately after a user is deemed eligible for the study, and prior to any other tasks (including any potential arm assignment).

However, there are many situations in which you may want to add other Informed Consent tasks that a user must agree to at other parts of the study.

ProofPilot considers Informed Consent to be an Intervention, though it is unlikely to have much of an effect on study outcomes. Only in rare situations would it be an intervention worthy of testing.

To add an a Consent task at any other point in the study, create an intervention, and choose the consent template.