Final answer:
General consent forms typically include informed consent with outlined risks and benefits, the preservation of confidentiality, and the protection of the participant from personal harm.
Step-by-step explanation:
General consent forms typically address a variety of issues to ensure that a person’s participation in a study or procedure is fully informed and voluntary. These consent forms often include the following:
- Seeking informed consent, which implies that all aspects of the study, including risks and benefits, are clearly outlined to the participant.
- Preserving confidentiality, assuring participants that their responses or health records will be kept private and protected.
- Protecting the subject from personal harm by ensuring that they are aware of potential risks and that measures to minimize them are in place.
By covering these aspects, consent forms respect the subject's privacy and dignity while guaranteeing that they are making a knowledgeable decision to participate.