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OSU School of Dentistry 20192020 Dental Explorer Program PARTICIPANT CONSENT FORM (Please complete consent form legibly in print.) INTRODUCTORY STATEMENT: Oregon Health & Science University (OSU)
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How to fill out participant consent form

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How to fill out participant consent form

01
Step 1: Start by addressing the participant and introducing yourself or your organization.
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Step 2: Explain the purpose of the consent form and what the participant's participation will involve.
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Step 3: Clearly outline the risks and benefits of participation, ensuring that the participant understands.
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Step 4: Provide a brief overview of the procedures or activities that the participant will be involved in.
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Step 5: Discuss any compensation or incentives that the participant may receive for their participation.
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Step 6: Explain the confidentiality measures and how the participant's data will be protected.
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Step 7: Clearly state that participation is voluntary and that the participant has the right to withdraw at any time without penalty.
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Step 8: Include a space for the participant to provide their signature and date the form.
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Step 9: Provide contact information for any questions or concerns the participant may have.
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Step 10: Ensure that the participant has fully read and understood the consent form before signing.
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Step 11: Make a copy of the signed consent form for your records.
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Step 12: Thank the participant for their time and willingness to participate.

Who needs participant consent form?

01
Any research study, clinical trial, or activity involving human participants requires a participant consent form.
02
This includes medical studies, psychological research, social science surveys, educational research, etc.
03
Consent forms are also needed for activities involving vulnerable populations such as children or individuals with disabilities.
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Informed consent is an ethical and legal requirement to ensure the rights and well-being of participants are protected.
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A participant consent form is a document that outlines the rights and obligations of individuals who are participating in a study, project, or event, seeking their agreement and informed consent to participate.
Typically, researchers, organizations, or entities conducting a study or activity that involves human participants are required to file a participant consent form.
To fill out a participant consent form, participants should read the entire form carefully, provide any required personal information, and sign and date the document to indicate their consent.
The purpose of a participant consent form is to ensure that individuals are fully informed about the scope, risks, and benefits of their participation, and to protect their rights throughout the process.
A participant consent form should report information such as the purpose of the study, procedures involved, risks and benefits, confidentiality assurances, and the participant's rights.
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