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Social & Behavioral Research: Forms & Consent Templates

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Non-Medical Investigators can find their relevant forms and consent templates in this section:

Protocol Submission Guidelines

  • When preparing a protocol for IRB submission, select the Non-Medical eProtocol Application category.
  • If your study involves collecting and analyzing human biological specimens or Protected Health Information (PHI), you must use the Medical eProtocol application.

Need Assistance?

Writing Consent/Assent Forms

  • Ensure that the language used is clear and 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

Template nameDocument type
Consent
doc [10/2025]
Research Information Sheet - Use for Waiver of Documentation
doc [10/2025]

Exempt Research Information Sheet

doc  [10/2025]
Parent or Legally Authorized Representative Permission
doc  [10/2025]
Video Use Consent
doc  [05/2023]

Assents, phone screens, scripts          

See consent template updates for recent changes

Template nameDocument type

Assent – under 18

doc [08/2025]
Telephone Screening of Potential Subjects  doc [05/2023]
 Sample Phone Screen Level 1a   Guidance 
Sample Phone Screen Level 1bScreen1a 
Oral Consent Scriptdoc [10/2025]
Research Payment Update Information Sheetdoc [02/2026]

Other Forms:

NHSR Determination; Other
Not Human Subject Research (NHSR) Determination Form
Letter of Agreement - for research in cooperation with other organizations
Social Behavioral Initial Submission Checklist
Scientific Review
Review of Scientific and Scholarly Validity, and Oversight (by Academic Sponsor)
Review of Scientific and Scholarly Validity (by Dept Chair or School Dean)

eProtocol Forms:

Required Attachments
International Research Supplemental Questions – research outside the US
DOE-supported research: Protection of Personally Identifiable Information (PII)    [Form APP-14]
Blank eProtocol Application Forms

      New, Modification, Continuing Review 

  (These are for informational purposes only)

eProtocol is used to submit: 
  • New Protocol applications - see examples above. 
      - Complete and attach supplemental required attachments as needed (see above) 
  • Modifications to approved protocols (need prior IRB approval to implement). 
  • Continuing Review applications. 
  • Reports unanticipated problems, events/information requiring prompt reporting. 
  • Final Reports (not required for Exempt research).