An informed consent document is a formal written agreement that gives prospective research participants the information needed to decide whether to participate. It protects participants by explaining the research, potential risks and benefits, and participant rights. section 8.1.2
A clear document typically includes:
- The research title and objectives, stated in language that readers can easily understand. section 8.1.2
- A precise project description covering participant steps and a realistic estimate of participation time. section 8.1.2
- Potential physical, emotional, and psychological risks, including discomfort or side effects. section 8.1.2
Survey participation summary
A survey may begin with a concise summary of its expected length, topics, and research-team contact information, helping respondents make an informed participation decision. section 8.1.2
Figure 8.2 An informed consent document for a survey conducted by a product analytics team
A product analytics survey consent document provides a concrete visual example of the format. section 8.1.2
