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Consent for Returning to Unperson Psychological Services This Consent is a supplement to the general informed consent that we agreed to at the outset of our clinical work together. Please read this
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How to fill out informed consent for in-person

01
Ensure that the informed consent form is provided to the participant before any data collection or intervention takes place.
02
Clearly explain to the participant the purpose of the study, the procedures involved, any risks or benefits, and their rights as a participant.
03
Allow the participant ample time to read and understand the informed consent form, and encourage them to ask any questions they may have.
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Once the participant has fully understood the information provided, have them sign and date the informed consent form.
05
Provide a copy of the signed informed consent form to the participant for their records.

Who needs informed consent for in-person?

01
Anyone who is participating in an in-person research study or clinical trial will need to fill out an informed consent form.
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Informed consent for in-person is a process where individuals are provided with information and details about a specific activity or procedure, and they voluntarily agree to participate or proceed.
Individuals who are participating in the in-person activity or procedure are required to file informed consent.
To fill out informed consent for in-person, individuals need to carefully read the provided information, understand the risks and benefits, and then sign the consent form.
The purpose of informed consent for in-person is to ensure that individuals are fully informed about the activity or procedure they are agreeing to, and that their choice to participate is voluntary.
The informed consent for in-person must include details about the activity or procedure, any risks involved, benefits, alternative options, confidentiality, and the right to withdraw consent.
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