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PARTICIPANT CONSENT FORM FOR SECONDARY DRIVER ONE YEAR VEHICLE DRIVING BEHAVIOR AND CRASH RISK STUDY (The SHIP 2 Naturalistic Driving Study) SPONSORS: National Academies of Science, Transportation
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How to fill out a participant consent form:

01
Start by reading through the entire form to understand the information and requirements it asks for.
02
Begin filling out the form by providing your personal information such as your name, address, date of birth, and contact details.
03
Next, carefully review the purpose of the study or event that the participant consent form is for. Make sure you understand what you are consenting to participate in.
04
If there are any risks or benefits associated with the study or event, carefully read and understand the section explaining them. It is important to be fully informed before giving your consent.
05
If you have any questions or concerns about the study or event, reach out to the responsible party or organization for clarification before proceeding with the form.
06
Once you have understood all the information on the form and are willing to participate, sign and date the consent form. Your signature indicates that you have willingly given your consent to participate.

Who needs a participant consent form:

01
Researchers: Researchers conducting studies or experiments that involve human participants need to obtain consent from those individuals. This is to ensure that participants are aware of the study's purpose, associated risks and benefits, and voluntarily agree to take part.
02
Event Organizers: Organizers of events or activities that involve participants, such as workshops, conferences, or sports tournaments, may require participants to sign a consent form. This form ensures that participants understand the nature of the event, any potential risks involved, and their agreement to participate.
03
Medical Practitioners: In certain medical procedures or treatments, especially those that involve experimental treatments or clinical trials, participants may be required to sign a consent form. This form ensures that patients understand the procedure, the associated risks, and provide their consent to proceed with the treatment.
In general, participant consent forms are necessary whenever an individual's participation is required in any study, event, or medical procedure, to protect their rights and ensure a clear understanding of the expectations and potential risks involved.
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The participant consent form is used to obtain permission from individuals before involving them in a research study or project.
Researchers and organizations conducting research studies or projects involving human participants are required to file participant consent forms.
To fill out a participant consent form, the researcher must provide detailed information about the study, risks and benefits involved, confidentiality measures, and obtain the signature of the participant.
The purpose of the participant consent form is to ensure that individuals are fully informed about the research study or project before agreeing to participate.
The participant consent form must include information on the study objectives, procedures involved, risks and benefits, confidentiality measures, and contact information for questions.
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