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Blood and Marrow Transplant Clinical Trials Network BMT CTN Protocol #1503 Version 3.0 dated January 16, 2018Informed Consent form for Transplant and Additional Follow Up as Part of a Research Study
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How to fill out informed consent and assent

01
Start by explaining the purpose of the study or research to the participant.
02
Provide the participant with all necessary information about the study, including potential risks and benefits.
03
Make sure the participant understands the information provided.
04
Allow the participant to ask any questions and clarify any doubts.
05
Provide the participant with enough time to consider their decision.
06
If the participant agrees to participate, ask them to sign the informed consent form.
07
If the participant is a minor, obtain assent from both the participant and their legal guardian or parent.
08
Keep a copy of the signed informed consent form for your records.

Who needs informed consent and assent?

01
Informed consent and assent are needed in research or medical studies that involve human participants.
02
This applies to both adult participants who are capable of giving consent and to 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 informed about the study and its potential risks and benefits before agreeing to participate.
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Informed consent is the process of informing individuals about the potential risks and benefits of participating in a study or treatment, while assent is obtaining agreement from individuals who may not be able to give full consent on their own, such as children or individuals with cognitive impairments.
Researchers, medical professionals, or individuals conducting studies or providing treatments that involve human participants are required to file informed consent and assent.
Informed consent and assent forms should be filled out completely and accurately, ensuring that all potential risks, benefits, and required information are clearly explained to the participants.
The purpose of informed consent and assent is to ensure that participants have all the necessary information to make an informed decision about their participation in a study or treatment, and to protect their rights and well-being.
Informed consent and assent forms should include details about the study or treatment, potential risks and benefits, confidentiality agreements, contact information for the researchers, and any other relevant information that participants need to know before agreeing to participate.
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