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SAMPLE INFORMED CONSENT FORM INSTRUCTIONS TO THE STUDENT RESEARCHER: An informed consent/assent/permission form like the version below should be developed in consultation with the student researchers
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How to fill out sample informed consent form

01
Start by reading the entire sample informed consent form to familiarize yourself with its contents.
02
Fill in the header section with the necessary information such as the title of the study, the name of the researcher, and the date.
03
Next, provide a clear and concise description of the study, including its purpose, procedures, risks, and benefits.
04
On the participant information section, ask for the participant's name, contact information, and any relevant demographic information.
05
Include a section that clearly explains the rights and responsibilities of the participant, such as their ability to withdraw from the study at any time.
06
Provide a space for the participant to indicate their consent by signing and dating the form.
07
Finally, include contact information for the researcher in case the participant has any questions or concerns.
08
Proofread the form for any errors or omissions before finalizing it.
09
Make copies of the form for the participant and the researcher's records.

Who needs sample informed consent form?

01
Researchers who are conducting studies that involve human participants need a sample informed consent form.
02
Institutional review boards (IRBs) or ethics committees responsible for reviewing and approving research studies may also need a sample informed consent form to ensure that the rights and well-being of participants are protected.
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A sample informed consent form is a document that outlines the details of a research study, including the risks and benefits involved, and obtains permission from participants to participate.
Researchers conducting a study requiring informed consent from participants are required to file a sample informed consent form.
To fill out a sample informed consent form, researchers must provide detailed information about the study, risks and benefits, and obtain signatures from participants.
The purpose of a sample informed consent form is to ensure that participants have all necessary information about a study before deciding to participate, and to protect their rights.
A sample informed consent form must include details about the study, risks and benefits, confidentiality measures, contact information, and participants' rights.
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