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INFORMED CONSENT FORM FOR PARTICIPATION IN A QUESTIONNAIRE BASED STUDY DEPARTMENT OF BIOMOLECULAR AND SPORT SCIENCES COVENTRY UNIVERSITY STUDY LEADER: Dr Pat Land, Senior lecturer, Coventry University
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How to fill out an informed consent form:

01
Read the form carefully: Begin by thoroughly reading the informed consent form to understand its purpose and requirements. Pay attention to any specific instructions or sections that need to be completed.
02
Provide personal information: The form will typically ask for your personal details such as your full name, contact information, date of birth, and any relevant identification numbers.
03
Understand the purpose: The informed consent form will outline the nature of the activity or procedure for which consent is required. Familiarize yourself with the details provided to ensure you fully comprehend what you are giving consent for.
04
Verify comprehension: Some informed consent forms will include a section where you need to confirm that you have had the opportunity to have any questions answered and that you fully understand the nature, risks, and benefits of the activity or procedure.
05
Consider risks and benefits: The form may require you to acknowledge that you have been informed about the potential risks and benefits associated with the activity or procedure. Take time to consider these factors before providing your consent.
06
Consultation and questions: If you have any doubts or concerns, it is essential to consult with the relevant professionals or experts who can address these questions before proceeding. Don't hesitate to clarify anything that is unclear.
07
Signature and date: Once you have carefully reviewed and understood the informed consent form, sign and date it as required. Your signature indicates that you voluntarily provide consent after understanding the relevant information.

Who needs an informed consent form:

01
Patients undergoing medical procedures: Individuals who are scheduled for surgery, medical treatments, or experimental therapies usually need to complete an informed consent form. This ensures they understand the risks, benefits, and alternatives associated with the procedure.
02
Participants in research studies: Individuals volunteering to participate in research studies are typically required to complete an informed consent form. This ensures they have a clear understanding of the purpose, procedures, potential risks, and possible benefits of the study.
03
Minors and their legal guardians: When medical procedures or research studies involve minors, their legal guardians must provide informed consent on their behalf. This ensures that the legal representatives are fully informed and making decisions in the best interest of the minor.
04
Activities involving potential risks: Any activity involving potential risks, such as extreme sports or adventure activities, may require participants to complete an informed consent form. This is to ensure individuals are aware of the inherent dangers and willingly assume the associated risks.
05
Miscellaneous situations: Informed consent forms may be necessary in various other scenarios, such as photography or videography releases, participation in counseling sessions, or even obtaining personal information for administrative purposes. The need for informed consent forms can vary depending on the specific circumstances and regulations in place.
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The informed consent form is used to ensure that a person understands the risks and benefits of a medical procedure or treatment before giving consent.
The individual receiving the medical procedure or treatment is required to file the informed consent form.
The informed consent form can be filled out by providing accurate information about the procedure, risks, benefits, and alternative options.
The purpose of the informed consent form is to protect the rights of patients by ensuring they have all the necessary information to make an informed decision about their medical care.
The informed consent form must include information about the procedure or treatment being performed, potential risks and benefits, alternative options, and the patient's right to refuse treatment.
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