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Name and Clinic NumberApproval Date: Not to be used after:June 3, 2020, June 2, 2021RESEARCH PARTICIPANT CONSENT AND PRIVACY AUTHORIZATION FORM Study Title: Pilot Study of the Effect of on Weight
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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
Clearly explain the purpose of the study to the participant.
02
Provide all necessary information about the study procedures, risks, benefits, and confidentiality.
03
Allow the participant to ask any questions and address any concerns they may have.
04
Have the participant read and understand the consent form before signing it.
05
Ensure that the participant receives a copy of the signed consent form for their records.

Who needs participant informed consent form?

01
Researchers conducting studies involving human participants.
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A participant informed consent form is a document that provides potential research participants with detailed information about a study, allowing them to understand what participation involves and to voluntarily agree to take part.
Researchers and institutions conducting studies that involve human participants are required to file a participant informed consent form.
To fill out a participant informed consent form, researchers should provide clear information about the study's purpose, procedures, potential risks and benefits, confidentiality measures, and participants' rights. Participants must sign the form to indicate their consent.
The purpose of a participant informed consent form is to ensure that participants are fully aware of what their involvement in a study entails, thus protecting their autonomy and rights.
The form must report information such as the study's purpose, procedures, duration, any risks or discomforts, potential benefits, confidentiality details, and contact information for questions or concerns.
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