Informed consent is a critical part of participating in any clinical study. It ensures that you understand the key facts about the research before deciding whether or not to participate. If you’re interested in joining a study, the research team will provide you with an informed consent document. This includes important information such as:
- The purpose and goals of the study
- Duration and number of visits
- Required procedures and tests
- Potential risks and benefits
- Your rights as a participant
- Contact information for questions or concerns
It’s the responsibility of the research team to explain this information clearly and answer any questions you may have. You’ll be given time to consider your options, speak with loved ones if needed, and make a decision that’s right for you.