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NCT04115228 Informed Consent Form INFORMED CONSENT TO PARTICIPATE IN A CLINICAL FEASIBILITY STUDY Title of Study: CLINICAL FEASIBILITY STUDY OF THE IMPLANTABLE TIBIAL NERVE STIMULATOR Principal Investigator:
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How to fill out informed consent form to

01
Here is a step-by-step guide on how to fill out an informed consent form:
02
Read the form carefully: Start by carefully reading the entire informed consent form to understand the purpose, risks, benefits, and procedures involved.
03
Seek clarification: If you have any questions or concerns about the form, don't hesitate to reach out to the person or institution responsible for providing the form. They should be able to address any uncertainties you may have.
04
Provide accurate personal information: Fill in your personal information accurately, including your name, contact details, and any other required identification information.
05
Understand the purpose: Make sure you understand the purpose of the study or procedure for which the informed consent is required. This will help you make an informed decision.
06
Consent statement: Carefully review the consent statement and ensure that you agree with the terms outlined. If you have any objections or reservations, discuss them with the relevant parties before signing the form.
07
Seek legal advice if necessary: If you have concerns about the legal implications of signing the consent form, consider seeking legal advice from a professional.
08
Signature and date: Sign and date the form to indicate your consent, acknowledging that you have understood the information provided and agree to participate.
09
Keep a copy: It's a good practice to retain a copy of the filled-out form for your records.
10
Remember, it's crucial to fully understand the implications of signing an informed consent form before proceeding with any study or medical procedure.

Who needs informed consent form to?

01
Informed consent forms are generally required by individuals who are participating in research studies, clinical trials, medical procedures, or any situation where their consent is necessary to proceed.
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This includes but is not limited to:
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- Patients undergoing medical treatments or surgeries
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- Participants taking part in scientific research studies
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- Volunteers participating in clinical trials
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- Individuals involved in psychological or behavioral experiments
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- Subjects participating in surveys or interviews
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- Donors of biological samples (blood, tissue, etc.) for research purposes
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In essence, anyone who needs to provide their informed consent in a formal and documented manner would be required to fill out an informed consent form.
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Informed consent form is a document that provides information to a person about a specific procedure, treatment, or research study, and allows them to make an informed decision about participating.
Healthcare providers, researchers, and institutions conducting medical procedures, treatments, or research studies are required to obtain informed consent from participants.
The informed consent form is typically filled out by the individual conducting the procedure or study, and it must include information about the purpose of the procedure or study, risks and benefits, and the participant's rights.
The purpose of the informed consent form is to ensure that participants have all the necessary information to make an informed decision about participating in a procedure or study, and to protect their rights.
The informed consent form must include information about the purpose of the procedure or study, risks and benefits, alternatives, confidentiality, and the participant's rights.
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