iRubric: Clinical Trial Simulation Video rubric

-The informed consent form includes all information relevant to the topic in an organized fashion:
Purpose of study, risks to the individual, benefits, confidentiality protection, compensation plan, contact information, and the participants’ rights during the study.

-Informed consent form includes all relevant information; however, it is not well-organized:
Purpose of study, risks to the individual, benefits, confidentiality protection, compensation plan, contact information, and the participants’ rights during the study.

-Does not have all of the relevant information of the informed consent form. Information is presented in an unorganized fashion: Purpose of study, risks to the individual, benefits, confidentiality protection, compensation plan, contact information, and the participants’ rights during the study.

-The informed consent form is lacking in elements required. There are many gaps in information presented. Missing many of these components: Purpose of study, risks to the individual, benefits, confidentiality protection, compensation plan, contact information, and the participants’ rights during the study.

The participants speak clearly and effectively. They efficiently shared information. It is evident that the student prepared what will be said.

The participants speak clearly and presents a good amount of the information expected.

There are several confusing moments and the information presented is not completely shared during the presentation. The student has not practiced what is to be said.

No preparation was done for the presentation and the information that is presented lacks many elements of what is expected.

Individual student displayed effort above and beyond expectations.

Individual student displayed effort that met the criteria for this project.

Individual student displayed some effort throughout this project.

Individual student was lacking in effort throughout this project.