Skip navigation links
Home
Contact OHRPPExpand Contact OHRPP
For ResearchersExpand For Researchers
Consent TemplatesExpand Consent Templates
Relying on Other IRBsExpand Relying on Other IRBs
Policies and GuidanceExpand Policies and Guidance
Education and TrainingExpand Education and Training
Post Approval Reporting
Quality ImprovementExpand Quality Improvement
For and About the IRBExpand For and About the IRB
For Research ParticipantsExpand For Research Participants
Other ResourcesExpand Other Resources
About the OHRPPExpand About the OHRPP
webIRB Home

Consent, Assent, and Screening Templates

 

Rather than dividing the templates into biomedical and behavioral templates, they are divided into the templates used for minimal risk studies, greater than minimal risk studies or for both. In addition, please see guidance and references at the bottom of this page. If you are unsure which template to use, please contact the OHRPP office.

 

IMPORTANT NOTE: Effective February 1, 2012 all new applications that require written consent forms must use one of the consent form templates below. Previous versions of the UCLA consent form templates are outdated and should not be used. With rare exceptions, new consent forms should include all applicable standards language and follow the layout of the new consent form templates.

 

Minimal Risk Research Informed Consent Templates (Expedited or Exempt)

 

back to top

Greater than Minimal Risk Research Informed Consent Templates (Full Committee Review)

 

back to top

Child and Adolescent Assent Templates

 

back to top

Addendum Consent Templates

 

back to top

Screening Scripts

 

back to top

Consent Standards and Sample Language

 

back to top

Comprehension Tools

 

back to top

Other References

 

back to top

Feedback

 

We appreciate your suggestions for improving templates and/or adding sample language to the standards documents. Please email OHRPPEQI@research.ucla.edu to provide your feedback.

back to top

 

Page Last Updated: October 23, 2013