Get the free Participant Informed Consent Form - Three Trusts

Project: Trust and Transcendence Page 1 Participant Informed Consent Form Please read this consent agreement carefully before you decide to participate in the study. Purpose of the research study:

How to fill out participant informed consent form

How to fill out a participant informed consent form:

1. Read and understand the form: Take the time to carefully read through the participant informed consent form. Familiarize yourself with all the sections and statements.
2. Provide personal information: Fill in your personal details such as name, age, address, contact information, and any other information required.
3. Understand the purpose: Ensure you understand the purpose of the study or research that you will be participating in. If you have any questions or concerns, discuss them with the researcher or study coordinator.
4. Review risks and benefits: Thoroughly read through the section that outlines the potential risks and benefits of participating in the study. Take note of any uncertainties or potential side effects.
5. Consent statement: Carefully read the consent statement and make sure you comprehend its content. By signing the form, you are indicating your voluntary agreement to participate in the study.
6. Clarify doubts: If there are any sections or terms that you are unsure about, do not hesitate to seek clarification. The researcher or study coordinator should be able to address any concerns or questions.
7. Seek additional information: If you feel the need to obtain more information about the study, request supplementary materials or contact the researcher for further details.
8. Ask for a copy: Request a copy of the fully completed consent form for your personal records. It is important to have a copy for reference.

Who needs a participant informed consent form:

1. Researchers: Researchers conducting studies or experiments that involve human participants are required to have a participant informed consent form. It ensures that participants are fully aware of the nature of the study, its purpose, potential risks, and benefits.
2. Institutional review boards (IRBs) or ethics committees: IRBs or ethics committees, responsible for reviewing research proposals, also require researchers to submit a participant informed consent form. This helps ensure that participants' rights and welfare are protected.
3. Participants: Individuals who are invited to take part in a research study or experiment will need to sign a participant informed consent form. This form allows them to make an informed decision about their participation and provides legal documentation of their consent.

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