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Page 1 Return to TABLE OF CONTENTSDepartment of Counselor Education & Counseling Psychology College of Education Marquette UniversityCounseling Psychology Ph.D. Program Handbook 20192020Page 2 Return
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How to fill out informed consent requirement

01
Provide clear and detailed information about the study or procedure to the participant.
02
Explain the purpose, risks, benefits, and alternatives to participation.
03
Ensure the participant's understanding by giving them an opportunity to ask questions.
04
Use simple and non-technical language, especially when dealing with participants who may have limited literacy or comprehension skills.
05
Obtain the participant's voluntary and informed consent in writing.
06
Include all necessary elements such as the purpose of the study, procedures involved, potential risks and benefits, confidentiality measures, and contact information for any further questions or concerns.
07
Provide a copy of the informed consent document to the participant for their records.
08
Regularly check for participant comprehension and address any concerns or misconceptions.
09
Document the informed consent process thoroughly.

Who needs informed consent requirement?

01
Medical researchers conducting clinical trials
02
Healthcare professionals performing medical procedures
03
Psychologists conducting research on human subjects
04
Academics conducting social science experiments involving human participants
05
Researchers in any field involving human subjects
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Informed consent requirement refers to the process by which a participant must be fully informed about the potential risks, benefits, and purpose of a study or procedure before agreeing to participate.
Researchers, institutions, and organizations conducting studies involving human subjects are required to file informed consent requirements.
To fill out the informed consent requirement, one must provide detailed information about the study, including the purpose, procedures, risks, benefits, confidentiality measures, and the participant's rights, and obtain a signature from the participant.
The purpose of the informed consent requirement is to ensure that participants are fully aware of what participation entails, to respect their autonomy, and to protect their rights and welfare.
The informed consent requirement must report information such as the study's purpose, procedures, potential risks and benefits, alternatives to participation, confidentiality assurances, and the participant's right to withdraw.
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