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Study Design Considerations: Consent
How do I design a consent process that promotes trust and inclusion?
Resources
Health Literacy in Clinical Research – Consent
Best practices for consenting participants in clinical trial studies developed by the Multi-Regional Clinical Trials Center.
Participant-Centered Informed Consent Training
Office for Human Research Protections (OHRP)
This 95-minute module from the Office of Human Research Protections trains you on how to write informed consent that is inclusive and clear for participants. It is a good resource for those in the research team involved in writing or obtaining informed consent from participants. Certificate available upon completion.
This 95-minute module from the Office of Human Research Protections trains you on how to write informed consent that is inclusive and clear for participants. It is a good resource for those in the research team involved in writing or obtaining informed consent from participants. Certificate available upon completion.
Templates – Consent and Recruitment
Downloadable consent, assent, parent consent, and recruitment templates from Kent State University.