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FOR IRB USE ONLY IRB ID #: 201508002 APPROVAL DATE: 07/23/20 RELEASED DATE: 07/23/20 EXPIRATION DATE: 05/25/21INFORMED CONSENT DOCUMENT Project Title:Exercise Training to Improve Brain Health in Older
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Read the informed consent document carefully and understand its purpose.
02
Provide your full name, date of birth, and contact information.
03
Fill in the project details, including the title, description, and objectives.
04
Specify any risks or potential benefits associated with participating in the project.
05
Indicate your willingness to participate and any conditions or restrictions.
06
Date and sign the consent document to indicate your understanding and agreement.
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Keep a copy of the signed document for your records.
08
Submit the completed informed consent document to the appropriate authority or project coordinator.

Who needs informed consent document project?

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Anyone participating in a research project or study that requires informed consent.
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The informed consent document project is a formal process through which participants are provided with essential information about a study, allowing them to make an informed decision about their participation.
Researchers and institutions conducting clinical trials or studies involving human participants are required to file informed consent documents.
To fill out the informed consent document, include details such as study purpose, procedures, risks, benefits, confidentiality, and participants' rights, ensuring clarity and understanding.
The purpose of the informed consent document is to ensure that participants are fully aware of the study's nature, risks, and benefits before agreeing to participate.
The informed consent document must report information including the study's purpose, procedures, potential risks and benefits, alternatives, confidentiality measures, and the participant's right to withdraw.
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