Simplified consent for non-interventional research focused on data collection and privacy. Ideal for surveys, registry studies, and natural history studies with minimal risk to participants.
The Observational Study consent template is designed for research that involves data collection without experimental interventions. This streamlined format focuses on what participants will do, how their data will be protected, and their rights during participation.
With eight focused sections, this template covers the essentials: introduction, purpose, activities, minimal risks, benefits, privacy protections, voluntary participation, and contact information. The language is accessible and straightforward, recognizing that observational studies typically pose fewer risks than interventional trials.
This template works well for survey-based research, patient registries, natural history studies, and quality-of-life assessments. It emphasizes data privacy and protection while maintaining a clear explanation of how participant information will be used and stored.
The simplified structure reduces participant burden while still meeting ethical requirements for informed consent in human subjects research.
This is a preview of the complete consent form experience participants will see.
Please provide your contact details
Please confirm you understand the following
Please sign below using your mouse or finger
Signature Area
Participants draw their signature here
Simplified format appropriate for minimal-risk observational research and data collection studies.