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INFORMED CONSENT TO PARTICIPATE IN A RESEARCH STUDY Full Study Title: Recovery Improved in covert Stroke with Exercise (RISE2) Principal Investigator: Investigator: Sponsor: Bradley Macintosh, PhD

How to fill out informed consent to participate

How to fill out informed consent to participate:

1. Begin by carefully reading the informed consent form provided by the research institution or organization. Understand the purpose, procedures, potential risks and benefits, and any other relevant details involved in the study.
2. If you have any questions or concerns, reach out to the research team or the appropriate contact person listed on the form. It is essential to have a clear understanding of what you are consenting to before signing the document.
3. Take your time to review each section of the form thoroughly. Pay attention to any checkboxes, fields, or signatures that may be required.
4. Provide accurate and honest information when filling out personal details such as your name, address, and contact information. It is crucial for the research team to be able to reach you if needed.
5. Make sure to highlight any specific sections that require your agreement or consent. These may include agreeing to participate voluntarily, understanding the potential risks and benefits, or granting permission for the use of your data.
6. If the form includes any optional sections, carefully consider whether you want to participate in those specific components of the study. You have the right to decline or choose which aspects you are comfortable with.
7. If the research involves minors or individuals who are unable to provide consent themselves, ensure that the appropriate legal guardian or representative signs and completes the necessary sections on their behalf.
8. Once you have completed filling out the form, review it again to ensure that you have provided all the required information and that your consent is clearly indicated.
9. Finally, sign and date the informed consent form as instructed. By doing so, you acknowledge that you have read and understood the information provided and are willingly participating in the study.

Who needs informed consent to participate?

1. Any individual who wants to participate in a research study, clinical trial, or any other form of research or data collection typically needs to provide informed consent.
2. Informed consent is especially crucial when the research involves human subjects and has the potential to impact their well-being, rights, or privacy.
3. Informed consent is required not only from adults capable of providing consent but also from parents or legal guardians if the research involves minors or individuals who are legally incapable of providing consent themselves.
4. Researchers and institutions are responsible for ensuring that informed consent is obtained before involving participants in their studies, as mandated by ethical guidelines and regulatory requirements.
5. Informed consent serves to protect the rights and welfare of participants, ensuring that they have an opportunity to understand the purpose and risks of the study before deciding to participate.

Overall, understanding how to fill out informed consent and who needs it is essential for anyone considering participating in a research study. By following the specified steps and guidelines, individuals can make informed decisions and protect their rights during the research process.

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What is informed consent to participate?

Informed consent to participate is the process of providing participants with information about a research study or project, including the risks and benefits involved, so they can make an informed decision about whether or not to participate.

Who is required to file informed consent to participate?

Researchers or project organizers are required to obtain and file informed consent to participate from all participants before they can take part in the study or project.

How to fill out informed consent to participate?

Informed consent forms typically include information about the study, risks and benefits, confidentiality, voluntary participation, and contact information for questions. Participants must read and sign the form to indicate their agreement.

What is the purpose of informed consent to participate?

The purpose of informed consent to participate is to ensure that participants are fully informed about the study or project before they agree to take part, and to protect their rights and well-being.

What information must be reported on informed consent to participate?

Informed consent forms should include details about the study or project, potential risks and benefits, confidentiality measures, voluntary participation, and contact information for questions or concerns.