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OUR WORKING RELATIONSHIP INFORMED CONSENT Welcome to Head/Heart Therapy! We are excited to have the opportunity to work with you and hope this handout will help you make an informed decision regarding
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To fill out the introduction to informed consent, follow these steps:
02
Start by providing a clear and concise title for the document, such as 'Introduction to Informed Consent Form'.
03
Include a brief overview of the purpose of the consent form, explaining how it relates to the research or medical procedure.
04
State that the consent form is intended to inform participants about the study or procedure, their involvement, and any potential risks or benefits.
05
Clearly explain the voluntary nature of participation and the right of participants to withdraw their consent at any time without facing any negative consequences.
06
Mention any compensation or benefits that participants may receive for their participation, if applicable.
07
Provide contact information for the researcher or healthcare professional responsible for the study or procedure, so participants can ask questions or seek clarification.
08
Include a space for the participant's signature and date, indicating their informed consent to participate.
09
Finally, ensure that the introduction to informed consent is written in plain language, avoiding jargon or complex terminology that may confuse participants.

Who needs introduction to informed consent?

01
Several groups of people may need introduction to informed consent:
02
- Researchers conducting scientific studies involving human participants.
03
- Healthcare professionals performing medical procedures or treatments that require informed consent.
04
- Clinical trial organizers and sponsors.
05
- Institutional review boards or ethics committees responsible for reviewing and approving research protocols.
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- Individuals participating in research studies or medical procedures, as they need to understand the risks and benefits before giving their informed consent.
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Informed consent is a process through which a participant voluntarily confirms their willingness to participate in a research study after being informed of all aspects that may influence their decision.
Researchers and institutions conducting studies that involve human subjects are required to file an introduction to informed consent.
To fill out an introduction to informed consent, a researcher must provide clear information about the study, its purpose, duration, procedures, risks, benefits, and the right to withdraw without suffering consequences.
The purpose of the introduction to informed consent is to ensure that participants understand the study and their role in it, enabling them to make informed decisions regarding their participation.
The information that must be reported includes the study's purpose, duration, procedures, potential risks and benefits, data confidentiality, and contact information for questions.
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