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Blood and Marrow Transplant Clinical Trials Network BMT CTN Protocol #1503 Version 3.0 dated January 16, 2018Informed Consent to Participate in Research Insert site logo and/or address TITLE: A Study
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How to fill out informed consent and assent

01
Read the informed consent and assent forms thoroughly to understand the purpose, risks, benefits, and procedures involved in the study.
02
Ensure that you have all the necessary information and resources to make an informed decision.
03
Consult with a legal guardian or parent if you are under the age of consent.
04
Complete all the required sections of the forms accurately and truthfully.
05
Sign and date the forms to indicate your consent or assent.
06
Ask any questions you may have before signing the forms.
07
Keep a copy of the forms for your records.

Who needs informed consent and assent?

01
Informed consent and assent are required for individuals who will be participating in research studies, clinical trials, or experiments.
02
This includes both adult participants who can give their own informed consent, as well as minors who may need to provide assent in addition to the consent of their legal guardian or parent.
03
Informed consent and assent ensure that participants are fully aware of the nature of the study, potential risks and benefits, and their rights before agreeing to participate.
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Informed consent is the process of providing all relevant information to a person before they can make a decision about participating in a research study. Assent is similar to informed consent, but is used for individuals who may not be able to provide full consent, such as children.
Research institutions and researchers conducting studies involving human subjects are required to obtain and file informed consent and, when applicable, assent.
Informed consent and assent forms typically include information about the study purpose, risks and benefits, procedures, confidentiality, and participant rights. Participants must sign the form to indicate their understanding and agreement.
The purpose of informed consent and assent is to ensure that individuals have all necessary information to make a voluntary and informed decision about participating in a research study.
Informed consent and assent forms must include details about the study, risks and benefits, procedures, confidentiality, and participant rights. The forms must also be written in a language that participants can understand.
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