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GREP Version 4 28.9.22Participant Information and Consent Form for online survey & physical function Research Project Title: dancing Care Evaluation NICE 3735 Background, aims of project You are invited
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How to fill out participant information and consent

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How to fill out participant information and consent

01
Provide the participant with a consent form to read and sign.
02
Make sure the participant understands the purpose of the study and their rights.
03
Request necessary personal information from the participant (name, age, contact details, etc.)
04
Record the participant's consent by having them sign the form.
05
Keep the participant information and consent form in a secure location.

Who needs participant information and consent?

01
Researchers conducting a study that involves human subjects
02
Institutional Review Boards (IRBs) overseeing research protocols
03
Government agencies or organizations requiring documentation for research purposes
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Participant information and consent includes details about an individual participating in a research study, along with their agreement to participate.
Researchers conducting a study are required to file participant information and consent.
Participant information and consent forms are typically filled out by the researcher and the participant, outlining details of the study and the participant's agreement to participate.
The purpose of participant information and consent is to ensure that individuals are fully informed about the research study and voluntarily agree to participate.
Participant information and consent should include details such as the nature of the study, risks and benefits, confidentiality agreements, and the participant's rights.
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