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PSYCHOTHERAPY INFORMED CONSENT I, by my initials at the bottom of each page, and my signature at the end of this document, attest that I have totally read and fully understand the following document.
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Step 1: Read the informed consent and authorization form carefully.
02
Step 2: Fill out your personal information, such as full name, date of birth, and contact details.
03
Step 3: Understand the purpose and nature of the study or procedure that requires consent.
04
Step 4: Consider the potential risks and benefits involved.
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Step 5: Ask any questions or seek clarifications from the researcher or medical professional.
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Step 6: Sign and date the form to indicate your informed consent and authorization.
07
Step 7: Keep a copy of the signed form for your records.

Who needs informed consent and authorization?

01
Informed consent and authorization is required of individuals who are participating in any research study, clinical trial, medical procedure, or treatment where their voluntary agreement and authorization are essential.
02
This includes patients in hospitals, participants in scientific research studies, individuals involved in experimental treatments, and candidates for certain medical procedures.
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Informed consent and authorization is a process through which a patient or participant is provided with adequate information about a procedure, treatment, or research study, enabling them to make an educated decision regarding their participation or treatment.
Healthcare providers, researchers, and organizations conducting medical procedures or research studies involving human subjects are typically required to file informed consent and authorization.
To fill out informed consent and authorization, the individual must provide their personal information, read the provided details about the procedure or study, indicate their understanding and agreement, and sign and date the form.
The purpose of informed consent and authorization is to ensure that individuals are fully aware of the risks, benefits, and purpose of a procedure or study, allowing them to make voluntary and informed decisions about their participation.
The information that must be reported includes the nature and purpose of the procedure or study, possible risks and benefits, alternatives, confidentiality safeguards, and the participant's rights, including the right to withdraw.
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