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Informed Consent Longer Version2016 American Society of Plastic Surgeons. Purchasers of the Informed Consent Resource are given a limited license to modify documents contained herein and reproduce
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How to fill out simplified informed consent resources

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Begin by providing the necessary background information about the study or procedure.
02
Clearly explain the purpose of the study and what it entails.
03
Describe all the risks and benefits associated with participating in the study.
04
Include details about any alternatives to participation and their potential consequences.
05
Use clear and concise language to ensure easy understanding by the participants.
06
Provide contact information for any questions or concerns that the participants may have.
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Ensure that the consent form includes a signature line for both the participant and the researcher.
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Review the filled-out consent form with the participant to address any doubts or questions.
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Keep a copy of the consent form on file for future reference and documentation purposes.

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Simplified informed consent resources ensure that individuals with various limitations can fully comprehend the information and make an informed decision.
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Simplified informed consent resources are tools or documents designed to help participants understand the nature of a study or procedure, ensuring they can make informed decisions about their participation with clearer and more accessible information.
Researchers and institutions conducting studies involving human participants are typically required to file simplified informed consent resources to adhere to ethical standards and regulatory guidelines.
To fill out simplified informed consent resources, you should provide clear, concise information about the study's purpose, duration, procedures involved, potential risks and benefits, and the rights of participants. Use straightforward language and avoid jargon.
The purpose of simplified informed consent resources is to ensure that participants are adequately informed about a study, enabling them to make knowledgeable decisions about their involvement and promoting ethical research practices.
Information reported must include the study's purpose, procedures, potential risks and benefits, confidentiality assurances, contact information for questions, and the voluntary nature of participation.
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