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INFORMED CONSENT FOR TELEPSYCHOLOGY This Informed Consent for Telepsychology contains important information focusing on doing psychotherapy using the phone or the Internet. Please read this carefully,
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Read the informed consent form carefully to understand the purpose, risks, benefits, and alternative options of the procedure or study.
02
Gather all necessary information and documents required to complete the form, such as personal identification details, medical history, and any relevant supporting documents.
03
Fill out the patient's personal information section accurately, including their full name, contact details, and date of birth.
04
Review and understand the statements and clauses mentioned in the form, including the nature of the procedure or study, the potential risks involved, and any potential side effects or complications.
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Who needs this informed consent for?

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The informed consent form is required for individuals who are participating in medical procedures, clinical trials, research studies, or any healthcare-related activities that involve potential risks or impacts on the participant's health or privacy.
02
It is also necessary for healthcare providers to obtain informed consent from patients before performing any procedures or treatments to ensure that the patient is fully aware and has given their consent based on understanding the relevant information.
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This informed consent is for obtaining permission from individuals before conducting a specific procedure or research study involving human participation.
Researchers or institutions conducting studies involving human subjects are required to file this informed consent.
To fill out this informed consent, provide clear information about the study, any risks involved, the purpose of the study, and ensure that consent is given voluntarily by the participant.
The purpose of this informed consent is to protect the rights and welfare of participants by ensuring they are fully informed about the study before agreeing to take part.
The informed consent must include details about the study's purpose, procedures, risks, benefits, confidentiality, and the right to withdraw at any time.
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