Search results
Results from the WOW.Com Content Network
A collection of informed consent, assent, and debriefing templates that can be used for your human participant research study.
• Use a file name(s) that clearly identify each consent document (e.g. online consent, parental permission, adult consent, teacher consent, screening consent, etc.). • In this template, “we” refers to the researchers.
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).
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.
These new templates should be used for any new consent form being submitted to the IRB. Required which contains all required elements of consent and HIPAA authorization. This is a special template that is required for use with iRIS. This form is referred to as the Personal Data Disclosure Form for Research Participants.
See IRB guidance on Children and Minors in Research for information about the documentation needed for consenting children and parents, and use the Sample Consent and Assent Forms for examples of how to write age-appropriate forms.
This consent form is designed specifically for obtaining either verbal or written consent to screen potential subjects in order to determine whether or not they are eligible to participate in a research study.