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Study Design Considerations: Consent
How do I design a consent process that promotes trust and inclusion?
Resources
Consent Guidelines for Equity in Research
Best practices for conducting the consent process with diverse populations developed by members of the Community Coalition for Equity in Research.
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.