For E-Consent to be valid, consent must always be completed in ‘SURVEY MODE’ as shown below:
To ensure users don’t mistakenly complete in ‘data entry mode’ you may add the below branching logic to each field within your consent document:
[is-survey]
If someone opens the ‘e-consent’ instrument in ‘data entry mode’ it will not display any fields, thus a user will be unable to mistakenly complete the e-consent incorrectly.
If you are working on FDA regulated study, please begin your consent process following: CFR Part 11 Validated Projects
For any NON-FDA studies, best practices are provided, however it may be the case that not all components mentioned are necessary for your specific study
Initial Considerations
Obtaining written consent is a critical step in the clinical research process. The type and extent of a project's e-Consent is driven by the project's IRB and is the responsibility of the Principle Investigator to ensure all IRB criteria are met and enforced. REDCap implements consent forms through an online survey.
How the e-Consent Framework functions
The REDCap e-Consent Framework provides standardized tools to obtain consent and store consent documentation with a certification screen and a storage function which automatically generates a ‘hard-copy' PDF of the signed form found in your projects ‘file repository’ application.
The below process includes steps on how you can setup your consents survey settings to automatically send the particpant a copy of their signed consent upon completion. Otherwise, if you only want to provide the signed consent upon a users request, use the ‘file repository’ to download > then send via email to participant, ensuring your email subject-line is encrypted since the document contains PHI!
Instructions on navigating the ‘file repository’ tool are linked above.
This article reviews the below topics:
e-Consent survey formats & Notes
How to create & build e-Consent survey
How participants use e-Consent
Assent and Parental Permission Forms
Consent Modification Process (only to be used when e-consent needs updated in Production)
e-Consent Survey Formats & Notes
Best practice is to upload each page of your consent document as an ‘in-line' displayed PNG or JPEG image.
WARNING: While the system will technically allow you to upload a single PDF that hosts all consent pages, this should NOT be done as it may cause the signed copy that gets saved to your project and/or sent to the participant to be blank! Example:
You may also create your e-consent by using a ‘in-line’ descriptive text field, however this does leave room for error and may be more difficult to update/version later on.
PNG or JPEG Image uploads
(best practice)
In-line descriptive text
No matter which format you choose, the end of each e-Consent survey should include your IRB Stamp of Approval and the below fields:
Additionally, be sure to include any discrete fields needed for your consent, such as storing images, genetic results, etc:
Consenting in multiple languages:
There are advanced features that can be used to ensure the participant is displayed only the consent images that are in their language using the MLM tool and branching logic. If you have questions on this setup, submit a REDCap help ticket.
How to create & build e-Consent survey:
Don’t want to build your E-Consent from scratch?
‘eConsent REDCap Template' is now available for use when requesting a new project be created:
How Participants Use e-Consent:
Assent and Parental Permission Surveys
Consent Modification Process
Design changes after the Production phase are discouraged but sometimes necessary. If a new version of the consent is needed, it is critical to modify the project in such a way as to not lose existing data nor compromise the audit trail of the REDCap e-Consent.
There are two ways to implement new versions of e-consent:
Creation of new instruments
Branching Logic
View process: Modify E-Consent: (version control)
Additional Considerations Related to e-Consent
Obtaining an eConsent that doesn't require a signature
Sometimes a study subject is unable to complete the signature due to physical handicap. Here are some suggestions which could be implemented to address this issue:
Use attestation form as provided above
Some low risk studies may not need a "wet" signature.
In this case you should still utilize e-consent framework, but the selection of the signature field is not required
These Knowledge Articles have been developed by the University of Utah’s REDCap Analysts using data garnered from the REDCap Consortium Library and other REDCap Affiliate members’ online resources and documents.