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Document Name:Informed Consent to Participate in Research, version 1.0Study Title:Clinical TransplantRelated Long term Outcomes of Alternative Donor Allergenic TransplantationProtocol:BMT CTN #1702NCT
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Read the informed consent form thoroughly to understand the purpose, procedures, and risks involved in the study.
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Who needs informed consent to participate?

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Informed consent to participate is required from any individual who wishes to take part in a research study or any medical procedure involving potential risks or unknown outcomes. This includes both adults and minors, although minors may require the consent of a parent or guardian depending on local regulations and the nature of the study.
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Informed consent to participate is a process through which a participant voluntarily confirms their willingness to participate in a study, after being informed of all relevant aspects that may affect their decision.
Researchers, institutions, or organizations conducting studies involving human participants are required to file informed consent to participate.
To fill out informed consent to participate, the researcher should provide clear and comprehensive information about the study, including its purpose, procedures, risks, benefits, and confidentiality measures, followed by obtaining the participant's signature.
The purpose of informed consent to participate is to ensure that participants are fully aware of what they are agreeing to and to protect their autonomy and rights within the research process.
Informed consent must report information such as the study's purpose, procedures, expected duration, potential risks and benefits, confidentiality measures, and contact information for questions.
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