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PARTICIPANT INFORMED CONSENT FORM (PICK) Protocol / Study number: Participant identification number for this trial: Title of project Name of Principal Investigator: Tel. No(s). The contents of the
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How to fill out participant informed consent form

01
Step 1: Provide a clear and concise title for the participant informed consent form.
02
Step 2: Include a brief introduction about the purpose of the study and what participation will entail.
03
Step 3: Explain the benefits and potential risks of participating in the study.
04
Step 4: Include a section that clearly states the voluntary nature of participation and that the participant has the right to withdraw at any time without penalty.
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Step 5: Detail the procedures and methods that will be used in the study.
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Step 6: Describe any confidentiality or privacy measures that will be taken to protect the participant's information.
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Step 7: Include contact information for the researcher or organization conducting the study, so participants can ask questions or raise concerns.
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Step 8: Provide space for the participant to sign and date the consent form, indicating their understanding and agreement to participate.
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Step 9: Keep a copy of the signed participant informed consent form for records.

Who needs participant informed consent form?

01
Researchers conducting scientific studies or experiments involving human participants typically need a participant informed consent form.
02
Medical professionals obtaining consent for procedures or treatments that carry potential risks or side effects also require a participant informed consent form.
03
Educational institutions, particularly when conducting research or surveys involving students, may require participant informed consent forms.
04
Any organization or individual conducting a study or experiment that involves human participants and requires their voluntary agreement to participate should use a participant informed consent form.
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Participant informed consent form is a document that provides detailed information to the participant about the research study, including its purpose, procedures, risks, and benefits. It also ensures the participant understands their rights and responsibilities.
Researchers conducting a study involving human participants are required to obtain and file participant informed consent forms.
To fill out a participant informed consent form, researchers must provide the necessary information about the study in clear and understandable language. Participants must then read and sign the form to indicate their understanding and agreement.
The purpose of participant informed consent form is to ensure that participants are fully informed about the research study, its risks and benefits, and their rights as participants. It also serves as documentation of the participant's agreement to participate.
Participant informed consent form must include information about the study's purpose, procedures, risks, benefits, confidentiality measures, voluntary participation, and the participant's rights.
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