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Attachment 1: Sample Informed Consent Form PARTICIPANT CONSENT FORM IN-VEHICLE DRIVING BEHAVIOR AND CRASH RISK STUDY (The SHRP2 Driving Behavior Stu y”) SPONSOR: National Academies, Transportation

How to fill out sample informed consent form

How to fill out a sample informed consent form:

1. Read the form thoroughly: Take the time to carefully review the entire consent form. Understand each section and the information it requires.
2. Provide personal information: Enter your full legal name, contact information, and any other requested personal details accurately. Make sure to include your current address, phone number, and email address.
3. Understand the purpose of the study or procedure: Familiarize yourself with the purpose of the study or procedure that requires your consent. It's important to grasp the potential risks, benefits, and alternatives involved.
4. Seek clarifications if needed: If there are any sections or terms in the consent form that you don't understand, don't hesitate to ask questions. Contact the appropriate person, such as a healthcare professional or researcher, for clarification.
5. Sign and date the form: Once you have comprehended the form and filled out all the required information accurately, sign and date it accordingly. This signifies your voluntary consent and acknowledges that you have read and understood the information provided.

Who needs a sample informed consent form?

1. Research participants: Individuals who are involved in research studies or clinical trials often need to provide their informed consent by signing a consent form. This ensures they have understood the nature of the study, its potential risks, and any benefits or alternatives.
2. Patients undergoing medical procedures: Informed consent forms are typically required for certain medical procedures, surgeries, or treatments. Patients are provided with information about the procedure and its potential risks and benefits. They then need to provide consent by signing the form.
3. Legal guardians or parents: In some cases, a sample informed consent form may be needed for minors or individuals who are unable to provide consent themselves. Legal guardians or parents may be required to sign the form on behalf of such individuals, ensuring they understand and agree to the procedure or study.

Overall, the purpose of a sample informed consent form is to ensure that individuals fully understand the nature of their involvement in a study or medical procedure. It serves as a legal document that signifies their voluntary consent based on access to relevant information.

For pdfFiller’s FAQs

What is sample informed consent form?

A sample informed consent form is a document that provides information to an individual about a research study, including the purpose of the study, potential risks and benefits, and the individual's rights and responsibilities if they choose to participate.

Who is required to file sample informed consent form?

Researchers conducting a study that involves human subjects typically need to obtain and file an informed consent form from each participant. The participants themselves are not required to file the form.

How to fill out sample informed consent form?

To fill out a sample informed consent form, you should read it thoroughly and understand the information provided. Then, you need to provide your personal information, indicate your consent to participate, and sign the form. It is important to ask any questions you may have and seek clarification before signing.

What is the purpose of sample informed consent form?

The purpose of a sample informed consent form is to ensure that individuals have been fully informed about a research study before they decide to participate. It aims to protect their rights and welfare by providing all necessary information and allowing them to make an informed decision.

What information must be reported on sample informed consent form?

A sample informed consent form typically includes information about the study's purpose, procedures, potential risks and benefits, confidentiality measures, compensation (if any), and the participant's rights and responsibilities. It may also include contact information for the research team in case of questions or concerns.

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