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Patient Label HereUNIVERSITY MEDICAL CENTER Lubbock, TexasDISCLOSURE AND CONSENT MEDICAL AND SURGICAL PROCEDURES TO THE PATIENT: You have the right as a patient to be informed about your condition
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Provide clear and detailed information about the study or treatment to the participant.
02
Explain the purpose of the study or treatment, as well as the potential risks and benefits involved.
03
Give the participant the opportunity to ask questions and seek clarification.
04
Ensure that the participant fully understands the information provided before proceeding.
05
Have the participant sign the consent form to indicate their agreement to participate voluntarily.

Who needs obtaining informed consent from?

01
Obtaining informed consent is necessary for all research studies involving human participants.
02
It is also required for medical treatments or procedures where the patient's consent is essential.
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Obtaining informed consent refers to the process of ensuring that participants in a study or procedure understand the risks and benefits before agreeing to take part.
Researchers, healthcare providers, and organizations conducting studies or medical procedures involving human subjects are required to file obtaining informed consent.
To fill out an informed consent form, provide clear information about the study or procedure, including objectives, risks, benefits, and participant rights, and ensure the participant signs it voluntarily.
The purpose of obtaining informed consent is to respect the autonomy of participants and ensure they are fully aware of what participation entails.
The form must include details such as the purpose of the study, procedures involved, risks and benefits, confidentiality assurances, and the right to withdraw at any time.
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