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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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How to fill out informed consent form study
01
Read the informed consent form carefully to understand the purpose of the study and what will be expected of you as a participant.
02
Make sure you understand all the risks, benefits, and any potential side effects associated with participating in the study.
03
If you have any questions or concerns, ask the researcher or study coordinator for clarification before signing the form.
04
Provide all the requested personal information accurately and honestly.
05
Sign and date the form to indicate your voluntary participation and agreement to abide by the study procedures.
06
Keep a copy of the signed informed consent form for your records.
Who needs informed consent form study?
01
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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What is informed consent form study?
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.
Who is required to file informed consent form study?
Researchers conducting the study are required to obtain and file the informed consent form from participants.
How to fill out informed consent form study?
The informed consent form should be completed by providing clear and detailed information about the study, risks, benefits, confidentiality, and participant rights.
What is the purpose of informed consent form study?
The purpose of the informed consent form is to ensure that participants are fully informed about the study and voluntarily agree to participate.
What information must be reported on informed consent form study?
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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