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BMT CLINICAL TRIALS NETWORK RICH Protocol 1204 Version 4.0 dated June 16, 2015, Informed Consent to Participate in Research Your Name: Study Title: ReducedIntensity Conditioning for Children and Adults

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What is informed consent and assent?

Informed consent is a process for obtaining permission from a patient or research participant before conducting a healthcare intervention. Assent is similar to informed consent but is used when the participant is a minor.

Who is required to file informed consent and assent?

Researchers, healthcare providers, and organizations conducting studies or interventions involving human subjects are required to file informed consent and assent.

How to fill out informed consent and assent?

Informed consent and assent forms typically include information about the study or intervention, potential risks and benefits, voluntary participation, confidentiality, and the rights of the participant. These forms must be carefully reviewed and signed by the participant or their legally authorized representative.

What is the purpose of informed consent and assent?

The purpose is to ensure that participants are fully informed about the research or intervention, understand the potential risks and benefits, and freely choose to participate.

What information must be reported on informed consent and assent?

The forms must include details about the study or intervention, risks and benefits, voluntary participation, confidentiality, and participant rights.

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