Social & Behavioral Research: Forms & Consent Templates

This section contains all of the forms and consent templates that apply to investigators from:  

  • Business 
  • Education 
  • Engineering 
  • Humanities & Sciences 
  • Law

*Please note that when creating a protocol for IRB submission, these investigators need to select the Non-Medical eProtocol Application category.

* Any study that involves the collection and analyses of human biological specimens and/or Protected Health Information (PHI) will need to be submitted on the Medical eProtocol application.

For questions, please contact the Non-Medical IRB Panel Staff.  If you are having trouble accessing these forms, please ask IRB Education (email or call 650-724-7141) to have them sent to you.

The consent/assent form should be in a language that is understandable to someone without a scientific background. Please use the Microsoft Readability Statistics tool as needed when writing your consent form.

Templates:

Consents           See consent template updates for recent changes
Consent	docx 05/2023
Research Information Sheet - Use for Waiver of Documentation	docx 05/2023
Exempt Research Information Sheet	docx  05/2023
Parent or Legally Authorized Representative Permission	docx  05/2023
Video Use Consent	doc  05/2023
Assents, phone screens, scripts           See consent template updates for recent changes
Assent – under 18	doc  05/2023
Telephone Screening of Potential Subjects    • Sample Phone Screen Level 1a    • Sample Phone Screen Level 1b	• Guidance  • Screen1a  • Screen1b
Oral Consent Script	docx  05/2023

Other Forms:

eProtocol Forms: