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Research Consent Form General Title of Research Project: Healthy Infants and Children Clinical Research Program (HICCUP) Investigators: Dr. Adam Kirkton (403) 9557424 Dr. David Johnson (403) 9557507
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How to fill out research consent form
How to fill out a research consent form:
01
Read the form carefully: Begin by thoroughly reading the research consent form. Make sure you understand all the information and sections included in the document.
02
Personal information: Fill in your personal information accurately. This usually includes your name, age, contact information, and any other relevant details requested. Be sure to provide up-to-date and correct information.
03
Understand the purpose of the research: Familiarize yourself with the purpose of the research study. This will help you make an informed decision before giving your consent to participate.
04
Informed consent section: Here, you will be provided with detailed information about the study, including its goals, procedures, potential risks and benefits, confidentiality agreements, and any compensation or incentives involved. Carefully review and understand this section before proceeding.
05
Ask questions: If you have any concerns or questions regarding the research study or the consent form itself, don't hesitate to ask the researchers. They should be available to provide clarifications and address any doubts you may have.
06
Sign and date: Once you have read and understood the consent form, you can sign and date it. This signature confirms that you voluntarily agree to participate in the research study and that you have been adequately informed about your rights and responsibilities.
Who needs a research consent form?
01
Researchers: Research consent forms are essential for researchers conducting studies involving human participants. These forms serve as legal documents that verify a participant's informed consent to participate in the study.
02
Institutional review boards (IRBs) and ethics committees: IRBs and ethics committees, which oversee research studies, require researchers to obtain consent forms from participants. These boards aim to ensure that studies are conducted ethically, protect participants' rights, and minimize potential harm.
03
Participants: Research consent forms are essential for participants as they provide crucial information about the study, its objectives, potential risks, and benefits. These forms inform participants of their rights and allow them to make an informed decision about whether or not to participate.
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What is research consent form?
Research consent form is a document that outlines the process of obtaining permission from individuals to participate in a research study.
Who is required to file research consent form?
Researchers conducting a study involving human subjects are required to file a research consent form.
How to fill out research consent form?
Research consent form can be filled out by providing detailed information about the study, risks and benefits, confidentiality, and participant rights.
What is the purpose of research consent form?
The purpose of research consent form is to ensure that participants are fully informed about the study and voluntarily agree to participate.
What information must be reported on research consent form?
Research consent form must include information about the study objectives, procedures, risks, benefits, confidentiality, and participant rights.
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