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IRB Consent Form Templates
A collection of informed consent, assent, and debriefing templates that can be used for your human participant research study.
General Consent Form Templates
Social and Behavioral Research Projects (last updated 03/16/2023)
Biomedical Research Projects (last updated 07/18/2022)
Consent Form Templates for Specific Biomedical Procedures
MRI and fMRI
Blood Collection by Finger Stick
Blood Collection by Venipuncture
Oral Consent Template
Guidance for Protocols Involving Oral Consent
Debriefing Template
Guidance and Template for Debriefing Participants
Studies Involving Children (Assent/Permission Forms)
Parent-Guardian Permission for Studies Involving Children
Sample Parental Notification Form
Sample Child Assent Form
Performance Release for Minors
Performance Releases
Performance Release for Adults
Sample consent and permission forms
General consent form to participate in research (DOC)
Two stage project consent form (DOC)
Parent permission form for research with child (DOC)
Child assent form (DOC)
Multiple consent form including audio-recording and quotations (DOC)
Photo and video consent form (DOC)
Video-recording consent form (DOC)
Re-contact agreement form (DOC)
Post-debriefing consent form (DOC)
Sample Consent Forms
Consent form templates.
These consent form templates have been posted for your reference. When completing and IRB submission in IRBIS, please fill in the application and use the consent form builder specific to your project. For more information, please find instructions here .
Summary of Changes to the Regulations for Informed Consent: Revised Common Rule Changes to Informed Consent and Waiver Requirements
Summary of Changes to Consent Documents:
- Informed Consent Documents – Version 2.0 Summary of Changes
- Informed Consent Documents – Version 2.1 Summary of Changes
- Informed Consent Documents – 10/26/2020 Summary of Changes
- Informed Consent Documents – 4/10/2023 Summary of Changes
Concise Summary examples can be found here .
Guidance on the use of plain language in consent forms:
- Clinical Research Glossary
- Webinar: The Promise of Plain Language: Launching a Glossary to Support Participant Understanding of Clinical Research – Recording & Slides
There are a few additional forms that are not provided online and may be accessed below. As needed, these should be completed and uploaded to your IRB application.
Foreign Language Consent Forms
COVID-19 Related Forms:
- Spanish-IRB-COVID Information Sheet
- Spanish COVID Consent Letter v2
- Spanish COVID Informational Sheet Translation Certificate
Informed Consent Short Form (for a single subject who may be illiterate, or otherwise unable to read the consent form — used when full consent form has to be read or translated for subject).
- Informed Consent Short Form Guidance
- Simplified Chinese
HIPAA Templates
- Sample HIPAA Authorization Template
- Sample HIPAA Authorization Template in Spanish ( Certification )
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General Consent Form Templates. Social and Behavioral Research Projects (last updated 03/16/2023) Biomedical Research Projects (last updated 07/18/2022) Consent Form Templates for Specific Biomedical Procedures. MRI and fMRI. Blood Collection by Finger Stick. Blood Collection by Venipuncture. Oral Consent Template. Guidance for Protocols ...
permission, adult consent, teacher consent, screening consent, etc.). • In this template, "we" refers to the researchers. If there is only one researcher, edit as appropriate. If the PI is a student, always use "we" to include the faculty advisor. • Submit consent documents in MS Word whenever possible. The iMedRIS comparison tool for
Consent • Your signature below indicates that you have decided to volunteer as a research participant for this study, and that you have read and understood the information provided above. You will be given a signed and dated copy of this form to keep, along with any other printed materials deemed necessary by the study investigators.
Considerations Before Writing the Consent Document. Tips for Developing a New Consent Form. Writing a consent form that uses plain language, and that is brief and clear, requires substantial effort. This effort can be lessened by using the consent template and adding the required information from the consent library (see more information below).
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General consent form to participate in research (DOC) Two stage project consent form (DOC) Parent permission form for research with child (DOC) Child assent form (DOC) Multiple consent form including audio-recording and quotations (DOC) Photo and video consent form (DOC) Video-recording consent form (DOC) Re-contact agreement form (DOC)
Consent Template Exempt Research ... This is an addendum to be used in conjunction with the consent form to allow participants to choose which genetic research results they would like to have returned to them. RoR Addendum: 6-13-2019: Signature Pages for Consent Forms
A research informed consent form is used to inform participants in a research study of how the research will be conducted, presented, and reported. The form also confirms the participants' consent to be part of the study, thus freeing the researchers conducting it of any liability. PDF Word ODT Updated November 15, 2024 4.6 Stars | 141 Ratings ...
When completing and IRB submission in IRBIS, please fill in the application and use the consent form builder specific to your project. For more information, please find instructions here. Summary of Changes to the Regulations for Informed Consent: Revised Common Rule Changes to Informed Consent and Waiver Requirements. Summary of Changes to ...
After the consent form expires or is superseded, iRIS will automatically void the consent document. If you need a copy for your records, please print out the consent form before it is voided. ... In that scenario, research participants will need to be informed about these screening and testing procedures. The following forms may be given to ...