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VA RESEARCH CONSENT FORM Subject Name:Date:Subject Initials: Principal Investigator:HARVARD YELLAPRAGADAVAMC:H50009 FEASIBILITY OF A TELEGAMEBASED EXERCISE (TELEEXERGAME) PROGRAM TO PREVENT DECONDITIONING
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Any individual who is participating in a research study or medical procedure that requires informed consent.
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The informed consent form is a document that outlines the details of a study or procedure, ensuring that participants understand the risks, benefits, and their rights before agreeing to participate.
Researchers and institutions conducting research involving human participants are required to file informed consent forms.
To fill out an informed consent form, provide clear information about the study, including its purpose, procedures, risks, benefits, confidentiality measures, and a contact for questions, followed by a space for participant signatures.
The purpose of the informed consent form is to ensure that participants voluntarily agree to participate in a study, fully understanding what it entails.
The informed consent form must report information such as study purpose, procedures involved, potential risks and benefits, confidentiality assurances, and the right to withdraw from the study.
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