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Approval Date: July 10, 2019,
Expiration Date: December 12, 2019RESEARCH CONSENT FORM
Title of Study: Online and Mobile Mindfulness
Principal Investigator: Jason Owen, Intervention to
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How to fill out research consent form
How to fill out research consent form
01
Read the research consent form carefully to understand its purpose and what it entails.
02
Provide all necessary personal information, such as your name, age, address, contact number, and email.
03
Ensure that you understand the purpose of the research project and its potential risks and benefits.
04
Take your time to comprehend the informed consent statement and ask any questions before signing the form.
05
If you have any concerns or doubts, consult with the research team or seek advice from a trusted professional.
06
Once you are satisfied with the information provided and have no further questions, sign and date the consent form.
07
Keep a copy of the signed consent form for your own records.
08
Remember that you have the right to withdraw your consent at any time during the research study.
Who needs research consent form?
01
Research consent forms are essential for anyone participating in a research study, whether as a participant, subject, or research subject.
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What is research consent form?
Research consent form is a document that provides detailed information about a research study to participants and outlines their rights and responsibilities.
Who is required to file research consent form?
Researchers conducting a study involving human subjects are required to file a research consent form.
How to fill out research consent form?
Research consent form can be filled out by providing accurate and complete information about the study, risks, benefits, and participant rights.
What is the purpose of research consent form?
The purpose of research consent form is to ensure that participants fully understand the study before agreeing to participate, and to protect their rights.
What information must be reported on research consent form?
Research consent form must include details about the study purpose, procedures, risks, benefits, confidentiality, voluntary participation, and contact information for questions.
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