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INFORMED CONSENT FORM PARTICIPANT Study Title: A Study of Cognitive Adaptation Training in Inpatient Forensic Environments Responsible Investigators: Sean Kidd 4165358501 ext. 6295, Center for Addiction
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How to fill out informed consent form participant
01
Read the informed consent form carefully to understand the purpose, procedures, risks, and benefits of the study.
02
Fill out your personal information accurately, such as your name, contact information, and any relevant medical history.
03
Understand any potential risks or side effects mentioned in the form and indicate your consent or preference regarding them.
04
Provide your signature, indicating that you have understood the information provided and consent to participate in the study.
05
Make sure to ask any questions or seek clarification from the research team before signing the form.
06
Keep a copy of the informed consent form for your reference.
Who needs informed consent form participant?
01
Any individual who is being invited or considering participating in a research study or clinical trial needs to fill out an informed consent form. This includes potential participants of medical studies, psychological studies, social science research, drug trials, etc.
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What is informed consent form participant?
An informed consent form participant is a document that outlines the details of a research study or medical procedure, ensuring that participants understand the purpose, risks, and benefits before agreeing to partake.
Who is required to file informed consent form participant?
Researchers or institutions conducting studies involving human subjects are required to file informed consent forms for their participants.
How to fill out informed consent form participant?
To fill out an informed consent form, participants should read the document carefully, ask questions if needed, and provide their signature to indicate their understanding and agreement to participate.
What is the purpose of informed consent form participant?
The purpose of an informed consent form is to protect participant rights by ensuring they are fully informed about the study and agree to participate without coercion.
What information must be reported on informed consent form participant?
The informed consent form must include information about the study's purpose, procedures, risks, benefits, confidentiality, and the right to withdraw at any time.
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