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INFORMED CONSENT FOR THE TREATMENT OF TRAUMATIC & DISSOCIATIVE DISORDERS1 This information is offered to give you important information about your treatment and provide you with an informed basis
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Who needs online informed consent for?

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Online informed consent is needed by individuals who are participating in research studies, clinical trials, or any other form of data collection where consent is required.
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It is also necessary for individuals who are accessing online platforms or services that collect personal information and require consent for its use.
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Researchers, healthcare professionals, and institutions designing and conducting studies or collecting data online also need to ensure that participants provide informed consent before proceeding.
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Online informed consent is used to ensure that individuals understand and agree to the terms and conditions of a service or procedure before participation.
Typically, institutions, researchers, or organizations that are conducting studies or services that involve participant data, medical procedures, or experiments are required to file online informed consent.
To fill out online informed consent, individuals usually need to read through the provided information, acknowledge their understanding of the terms, and provide their digital signature or agreement.
The purpose of online informed consent is to protect the rights of participants by ensuring they are fully informed about what they are agreeing to, including any risks involved.
Information that must be reported includes the purpose of the study, procedures involved, potential risks, benefits, confidentiality assurances, and the right to withdraw.
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