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The University of Sheffield Unit of Academic Radiology School of Medicine, Royal Hallamshire Hospital Researcher: Prof Paul Griffiths MERIDIAN Add on study, Ethics reference: 11/OH/0006 Patient Identification
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How to fill out a study consent form:

01
Read the study consent form carefully to understand its purpose and requirements.
02
Provide your personal information such as name, contact details, and any other information requested in the form.
03
Review the information about the study, including its objectives, procedures, potential risks, and benefits.
04
Make sure to ask any questions or seek clarification from the researchers if something is unclear.
05
If you agree to participate in the study, sign and date the consent form.
06
If you do not wish to participate or have any concerns, you can choose not to sign the form and inform the researchers accordingly.
07
Keep a copy of the consent form for your records.

Who needs a study consent form:

01
Individuals who are invited or recruited to participate in research studies.
02
Participants under the legal age may require the consent of their parent or guardian to sign the form.
03
In some cases, individuals with limited mental capacity may have a legal representative authorize their participation by signing the consent form on their behalf.
04
Researchers and institutions conducting the study often require participants to provide informed consent to ensure ethical and legal considerations are met.
05
The study consent form acts as documentation to protect both the participants and the researchers involved in the study.
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The study consent form is a document that explains the research study to the participants and provides them with all the necessary information to make an informed decision on whether to participate.
Researchers conducting a study involving human subjects are required to file a study consent form.
The study consent form can be filled out by providing all the required information about the study, risks, benefits, and participant rights.
The purpose of the study consent form is to ensure that participants have been fully informed about the study, and voluntarily agree to participate.
The study consent form must include information about the study purpose, procedures, risks, benefits, confidentiality, and participant rights.
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