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NCT04187989 Official Title: Social Media Intervention for Cannabis Use in Emerging Adults Date of IRB Approval: 8/22/2019UNIVERSITY OF MICHIGAN CONSENT TO BE PART OF A RESEARCH STUDY 1. KEY INFORMATION
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How to fill out informed consent form template
How to fill out informed consent form template
01
Read through the entire informed consent form thoroughly to understand the information you are agreeing to.
02
Fill out personal information accurately, such as your name, date of birth, and contact details.
03
Acknowledge any risks or potential side effects associated with the research or procedure.
04
Sign and date the form to indicate your understanding and agreement to participate.
05
Make a copy of the completed informed consent form for your records.
Who needs informed consent form template?
01
Individuals participating in research studies
02
Patients undergoing medical procedures
03
Participants in clinical trials or experimental treatments
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What is informed consent form template?
The informed consent form template is a document that outlines all the relevant information regarding a study or medical procedure and ensures that participants are aware of the risks and benefits before giving their consent.
Who is required to file informed consent form template?
Researchers, doctors, and other medical professionals conducting studies or procedures that involve human subjects are required to file informed consent form templates.
How to fill out informed consent form template?
To fill out an informed consent form template, the individual must carefully read and understand all the information provided, then sign the document to indicate their consent.
What is the purpose of informed consent form template?
The purpose of the informed consent form template is to protect participants by ensuring they have all the necessary information to make an informed decision about participating in a study or procedure.
What information must be reported on informed consent form template?
The informed consent form template must include details about the study or procedure, potential risks and benefits, participant rights, confidentiality, and contact information for questions or concerns.
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