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INFORMED CONSENT TO RECEIVE PSILOCYBIN SERVICESIntroduction:In the State of Oregon, psilocybin services are delivered during three different sessions: preparatory, administration, and integration.
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How to fill out draft informed consent form

01
Step 1: Read the entire draft informed consent form carefully to understand its content and purpose.
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Step 2: Fill in the personal and contact information accurately.
03
Step 3: Understand the purpose of the study or research being conducted and make sure it is clearly mentioned in the form.
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Step 4: Provide your signature, indicating that you have understood the content and voluntarily give your informed consent.
05
Step 5: If there are any sections or terms that you do not understand, seek clarification from the researcher or study coordinator before signing.
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Step 6: Review the risks and benefits associated with participating in the study, and make an informed decision about whether to give consent.
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Step 7: If you have any reservations or concerns, discuss them with the study team before signing the form.
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Step 8: Keep a copy of the filled consent form for your records.

Who needs draft informed consent form?

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Anyone who is going to participate in a research study or a medical procedure that requires informed consent needs a draft informed consent form. This includes individuals who are volunteering for clinical trials, participating in surveys, undergoing surgical procedures, or taking part in any type of experimental treatment or research.

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A draft informed consent form is a document that outlines the information given to participants about a study or clinical trial, ensuring that they understand the purpose, procedures, risks, and benefits before agreeing to participate.
Researchers and institutions conducting studies involving human participants are required to file a draft informed consent form with the relevant regulatory bodies before commencing the study.
To fill out a draft informed consent form, include details such as the study title, purpose, expected duration, procedures, potential risks, benefits, confidentiality measures, and contact information for inquiries.
The purpose of a draft informed consent form is to ensure that participants are fully informed about a study, can ask questions, and provide consent voluntarily, thereby protecting their rights and well-being.
Information that must be reported includes the study's aims, procedures, duration, risks and benefits, confidentiality assurances, contact details for researchers, and a statement of voluntary participation.
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