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This document serves as a consent form regarding the processing of personal data by the National Research University Higher School of Economics (HSE). It outlines the types of personal data collected,
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How to fill out informed consent

How to fill out informed consent
01
Begin by clearly stating the purpose of the consent form.
02
Provide a detailed description of the procedure or treatment being consented to.
03
Explain the potential risks and benefits involved.
04
Include information about alternatives to participation or treatment.
05
Outline the rights of the participant, including the right to withdraw at any time.
06
Ensure the participant understands the information provided; encourage questions.
07
Provide space for the participant's signature and date.
Who needs informed consent?
01
Participants in clinical trials or research studies.
02
Patients undergoing medical treatments or procedures.
03
Individuals involved in psychological assessments or interventions.
04
Subjects in educational or behavioral research.
05
Minors, typically requiring parental or guardian consent.
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What is informed consent?
Informed consent is a process by which a person voluntarily confirms their willingness to participate in a particular treatment or research study after being informed of all relevant aspects, including potential risks, benefits, and alternatives.
Who is required to file informed consent?
Researchers, healthcare providers, and institutions conducting clinical trials or medical procedures are generally required to obtain and file informed consent from participants or patients.
How to fill out informed consent?
To fill out informed consent, individuals should carefully read the consent form, ask any questions they have, ensure they understand the information provided, and then sign the form to indicate their agreement to participate.
What is the purpose of informed consent?
The purpose of informed consent is to ensure that individuals are fully aware of what they are agreeing to, enabling them to make informed decisions regarding their participation in research or treatment.
What information must be reported on informed consent?
Informed consent must include information about the purpose of the study, procedures involved, risks and benefits, alternatives to participation, confidentiality, and a statement that participation is voluntary.
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