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INFORMED CONSENT FORM STUDY TITLE: ISCHEMIC CONDITIONING IMPROVES WALKING FUNCTION POST STROKE DATE OF DOCUMENT: 7/26/2019INSTITUTIONAL REVIEW BOARD Informed Consent for Research Protocol Number:
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Read the informed consent form carefully to understand the purpose of the study and what will be expected of you as a participant.
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Make sure you understand all the risks, benefits, and any potential side effects associated with participating in the study.
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Sign and date the form to indicate your voluntary participation and agreement to abide by the study procedures.
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Who needs informed consent form study?

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Anyone who will be participating in a research study or clinical trial needs to fill out an informed consent form. This includes individuals who have been invited to participate as subjects in a study.
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Informed consent form in study is a document where participants voluntarily agree to participate after being informed about the study's purpose, procedures, risks, and benefits.
Researchers conducting the study are required to obtain and file the informed consent form from participants.
The informed consent form should be completed by providing clear and detailed information about the study, risks, benefits, confidentiality, and participant rights.
The purpose of the informed consent form is to ensure that participants are fully informed about the study and voluntarily agree to participate.
The informed consent form should include details about the study's purpose, procedures, risks, benefits, confidentiality, voluntariness, and contact information for researchers.
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