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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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01
Read the form thoroughly: Start by carefully reading the research consent form. Make sure you understand all the information provided and any terms or conditions mentioned.
02
Enter personal information: Fill out the required personal information accurately. This typically includes your name, contact details, age, gender, and any other relevant details as requested.
03
Understand the purpose of the research: Familiarize yourself with the purpose and objectives of the research study. This will help you comprehend the significance and potential impact of your participation in the study.
04
Consent statement: Carefully read the consent statement, which outlines the purpose of the study, potential risks or benefits, procedures involved, and the voluntary nature of your participation. Ensure that you understand all the details mentioned.
05
Seek clarification: If you have any questions or concerns regarding the research study or the consent form, don't hesitate to seek clarification from the researchers or study coordinator. It is crucial to have a clear understanding before providing your consent.
06
Make an informed decision: Based on the information provided in the research consent form, assess whether you are comfortable participating in the study. Consider the potential risks, benefits, and any possible impact on your privacy or confidentiality. Make an informed decision that aligns with your values and preferences.
07
Provide consent: If you are willing to participate and have understood all the information presented, sign the consent form indicating your agreement to participate voluntarily. Some forms may also require a witness signature if applicable.
08
Keep a copy: Before submitting the consent form, make sure to keep a copy for your own records. This will ensure that you have a reference of the details you agreed to in case you need to review them later.

Who needs research consent form?

01
Individuals participating in the research study: Research consent forms are required for individuals who are going to be involved in the research study. This could include participants, subjects, or patients who are being recruited for the study.
02
Researchers and study coordinators: Researchers and study coordinators also play a crucial role in the research process. They need to ensure that participants provide informed consent before commencing any research activities.
03
Institutional review boards (IRBs): IRBs, ethics committees, or similar regulatory bodies are responsible for reviewing and approving research studies. They require researchers to obtain valid consent from participants and ensure the ethical conduct of the research.
04
Legal and ethical standards: In many countries, obtaining informed consent from participants is legally mandated to protect individual rights and welfare. Ethically, it ensures that participants are aware of the study's objectives, procedures, risks, and potential benefits, allowing them to make an autonomous decision on participating or withdrawing from the study.
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Research consent form is a document that outlines the details of a research study, including its purpose, procedures, risks, benefits, and the rights of participants.
Researchers conducting studies involving human subjects are required to obtain and file research consent forms from participants.
Research consent forms can be filled out by providing personal information, acknowledging understanding of the study details, and signing the form to indicate consent.
The purpose of research consent form is to ensure that participants are fully informed about the study and voluntarily agree to take part in it.
Research consent forms must include details about the study's purpose, procedures, risks, benefits, confidentiality measures, and the rights of participants.
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