From: Personalized and long-term electronic informed consent in clinical research: stakeholder views
Recruitment | Dropout | Understanding |
---|---|---|
Positive impact | Positive impact | Positive impact |
Would be facilitated, especially for rare diseases | Frequent updates could keep participants interested | Interactive tools could facilitate comprehension and retention of knowledge |
More diverse population | Participants could have a better understanding of what to expect | Implementation of metrics could support physicians when explaining the research study |
Negative impact | Negative impact | Negative impact |
---|---|---|
Could widen the digital gap | Electronic systems could be too complicated | Information overload |
Would be difficult to establish a relationship of trust | Participants may stop participating due to less personal contact | Â |