Final answer:
Electronic informed consent in research studies requires clear outline of risks and benefits, transparent research intentions, and a protocol for participant protection.
Step-by-step explanation:
Electronic informed consent in research studies requires additional components to ensure the safety and rights of participants. These components include:
- Clear outline of risks and benefits: Participants should be fully informed about the potential risks and benefits of the study in order to give appropriate consent.
- Transparent research intentions: Researchers must clearly explain the purpose of the study and how the data will be used in the future.
- Protocol for participant protection: Research plans should specify whether recordings, notes, and data will be archived or destroyed at the end of the project.