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PARTICIPANT INFORMED CONSENT FORM (PICF) (English) Protocol / Study number :___ Participant identification number for this trial: ___ Title of project: Reliability of ultrasonographic skeletal muscle
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How to fill out participant informed consent form

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How to fill out participant informed consent form

01
Provide clear and detailed information about the study to the participant.
02
Explain the purpose of the study and the procedures involved.
03
Describe any potential risks or benefits to the participant.
04
Ensure that the participant understands that their participation is voluntary.
05
Answer any questions the participant may have about the study.
06
Have the participant sign and date the form to indicate their informed consent.

Who needs participant informed consent form?

01
Researchers conducting studies involving human participants.
02
Medical professionals obtaining consent for treatment or procedures.
03
Organizations conducting surveys or interviews with participants.
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A participant informed consent form is a document that provides potential participants with detailed information about a study or research project, allowing them to make an informed decision about their participation.
The research team or organization conducting the study is required to file a participant informed consent form.
To fill out a participant informed consent form, one must provide clear information about the study, the purpose, procedures, potential risks, benefits, and contact information for inquiries, ensuring that participants understand what they are agreeing to.
The purpose of the participant informed consent form is to ensure that participants are fully aware of the nature of the study and their rights, which helps protect them and uphold ethical standards in research.
The participant informed consent form must report information such as the study's purpose, procedures, risks, benefits, confidentiality measures, and the voluntariness of participation.
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