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Protocol 20190182 March 21, 2022 Page 1 of 8Informed ConsentINFORMED CONSENT/AUTHORIZATION FOR PARTICIPATION IN RESEARCH WITH OPTIONAL PROCEDURES Texas State HPV SelfCollection Pilot Study 20190182
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Begin by reading the entire informed consent form carefully to understand its purpose.
02
Fill in any required personal information, such as your name, date of birth, and contact details.
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Review the information provided about the study or procedure, including its risks and benefits.
04
Make sure you understand your rights and the option to withdraw consent at any time without penalty.
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Ask any questions you may have to ensure clarity about the information presented.
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Sign and date the consent form where indicated to confirm your agreement.

Who needs informed consent form form?

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Participants in clinical trials or research studies.
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Patients undergoing medical procedures or treatments.
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Individuals involved in psychological evaluations or interviews.
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Minors, where legal guardians are required to provide consent on their behalf.
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An informed consent form is a document that individuals must sign to indicate they understand the procedures, risks, and benefits of participating in a study or medical treatment.
Researchers, healthcare providers, and institutions conducting studies or medical treatments that involve human participants are required to file an informed consent form.
To fill out an informed consent form, one must provide clear information about the study or treatment, including its purpose, procedures, risks, benefits, and the rights of the participants, along with a space for the participant's signature.
The purpose of an informed consent form is to ensure that participants are fully aware of what they are agreeing to and to protect their rights and autonomy in the decision-making process.
The informed consent form must report information such as the study's objectives, procedures, potential risks, benefits, confidentiality measures, and the participant's right to withdraw at any time.
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