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EA1141 NCT02933489INFORMED CONSENT FOR PARTICIPATION IN A CLINICAL TRIAL Connecting Hope and Medical ScienceStudy Title for Study Participants: Comparison of Mammography to a Fast MRI in Breast Cancer
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How to fill out informed consent for participation

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How to fill out informed consent for participation

01
Read the informed consent document thoroughly to understand the purpose, risks, benefits, and procedures of the study.
02
Consult with the research team or experts if you have any questions or concerns about the study.
03
Fill out the participant information section accurately, providing your name, contact details, and other requested information.
04
Review the study requirements and make sure you meet the criteria for participation.
05
Understand and acknowledge any potential risks or side effects associated with the study.
06
Sign and date the consent form to indicate your agreement to participate voluntarily.
07
If applicable, ensure that a parent or guardian also signs the consent form for participants who are minors.
08
Keep a copy of the informed consent form for your records.
09
Stay informed throughout the study and ask for updates or clarification whenever necessary.
10
Remember that participation is entirely voluntary, and you can withdraw from the study at any time without penalty.

Who needs informed consent for participation?

01
Informed consent for participation is needed for any individual who wishes to take part in a research study or medical trial.
02
This can include patients, healthy individuals, volunteers, or minors, depending on the specific study and its requirements.
03
Informed consent ensures that participants understand the purpose, risks, benefits, and procedures of the study, and allows them to make an informed decision about their involvement.
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Informed consent for participation is a process where individuals are provided with information about a study or project and voluntarily agree to participate based on that information.
Researchers or study organizers are required to obtain and file informed consent for participation from potential participants.
Informed consent forms are typically filled out by including information about the study, risks and benefits, confidentiality, and participant rights, and obtaining signatures from participants.
The purpose of informed consent for participation is to ensure that participants are aware of what they are agreeing to, understand the risks and benefits of participation, and are able to make an informed decision about joining the study or project.
Informed consent for participation should include details about the study, potential risks and benefits, confidentiality measures, contact information for questions, and participant rights.
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