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EC# 134001302 Treatment for Multidisciplinary Professionals October 23, 2012, STATEMENT OF INFORMED CONSENT The Great Lakes ATC is interested in determining the impact of this program on participants'
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Start by reading the statement of informed consent thoroughly. Make sure you understand the purpose and implications of the document.
02
Provide your personal information accurately. This may include your full name, contact details, date of birth, and any other required identifying information.
03
Review the purpose and nature of the study or procedure. Understand what is being asked of you and any potential risks or benefits involved.
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Carefully read through each section of the statement of informed consent. It may cover topics such as the purpose of the study or procedure, potential risks and side effects, confidentiality and privacy considerations, and your rights as a participant.
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If you have any questions or concerns, don't hesitate to ask the person administering the document. It's important to have a clear understanding before signing.
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Once you are satisfied with the information provided, sign and date the statement of informed consent. By doing so, you are confirming that you understand the details outlined in the document and you willingly agree to participate or undergo the procedure.

Who needs a statement of informed consent:

01
Researchers conducting studies that involve human subjects require participants to sign a statement of informed consent. This ensures that participants are fully aware of the details and potential risks involved in the research.
02
Medical professionals may require patients to sign a statement of informed consent before performing certain procedures or treatments. This helps ensure that patients have a complete understanding of the procedure, possible risks, and alternative options before giving their consent.
03
Informed consent is also necessary in various other fields, such as psychology, education, and legal research, where individuals may be asked to participate in studies or interventions that impact their rights or well-being.
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The statement of informed consent is a document that outlines the details of a study or research project and ensures that participants are fully informed of the risks and benefits before they agree to participate.
Researchers or individuals conducting a study that involves human participants are required to file a statement of informed consent.
The statement of informed consent should be filled out by providing all necessary information about the study, risks, benefits, confidentiality, and contact information for questions.
The purpose of the statement of informed consent is to protect the rights and wellbeing of participants in research studies by ensuring they have all relevant information before agreeing to participate.
The statement of informed consent must include details about the study, risks and benefits, confidentiality measures, contact information for questions, and the participant's rights.
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2012 Illinois ATTC ATTCs UIC Bennett Multidisciplinary identifier questionnaires Institutional populations EC surveys digit participants determining abusing completion responses

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