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RESEARCH CONSENT FORM DO NOT PLACE IN MEDICAL RECORD Protocol Title: Genetics of Epilepsy and Cognitive Disorders Principal Investigator: Christopher Walsh Use Plate or Print: Subject Name: DOB: Gender:
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How to fill out research consent form

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How to fill out a research consent form:

01
Read the form thoroughly: Begin by carefully reviewing the entire research consent form. Make sure you understand all the information and requirements stated in the document.
02
Provide personal information: Fill in your full name, date of birth, and contact information accurately. This information is essential for identification and communication purposes.
03
Understand the purpose of the research: Take your time to comprehend the purpose and objectives of the research project. This will help you make an informed decision about whether to give your consent or not.
04
Review the risks and benefits: Pay attention to the potential risks and benefits associated with participating in the research. This information should be clearly outlined in the form. If you have any concerns or questions, don't hesitate to seek clarification from the researchers.
05
Comprehend the procedures: Familiarize yourself with the procedures involved in the research. Understand what will be expected of you as a participant, including any tests, interviews, or interventions that may be involved.
06
Clarify confidentiality and data handling: Ensure that the consent form outlines how your personal information and data will be handled and kept confidential. It should also mention any data sharing or publication plans. If you have concerns about this, discuss them with the researchers.
07
Ask questions: If anything is unclear or if you have any concerns, it is important to ask questions before signing the consent form. The researchers should be available to address any doubts or provide additional information.
08
Sign and date the consent form: After thoroughly understanding the contents of the research consent form, sign and date it accordingly. By doing so, you are indicating that you have voluntarily agreed to participate in the research project.

Who needs a research consent form:

01
Participants in a research study: Anyone who is being asked to participate in a research study, regardless of age or background, typically needs to sign a research consent form. It ensures that the participants are fully informed about the study and willingly agree to be part of it.
02
Legal guardians or parents: If the research involves minors or individuals who are unable to provide informed consent themselves, their legal guardians or parents are required to sign the research consent form on their behalf.
03
Additional parties involved: In some cases, other parties involved in the research study, such as healthcare providers or data custodians, may be required to sign a research consent form to ensure compliance and transparency. This ensures that all parties involved understand their roles and obligations.
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Research consent form is a document that outlines the purpose of a research study, risks and benefits involved, and ensures that participants voluntarily agree to participate.
Researchers conducting a study that involves human subjects are required to file a research consent form.
Research consent forms are typically filled out by providing information about the study, risks and benefits involved, and obtaining signatures from participants.
The purpose of a research consent form is to ensure that participants have been fully informed about the study and voluntarily agree to participate.
Research consent forms must include information about the study purpose, risks and benefits, confidentiality, and participant rights.
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