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Online ICF Version 1.6 29Sep20IRAS number: 27844CONSENT FORM FOR PARTICIPANTS IN RESEARCH STUDIES Online Screening Please complete this form after you have read the Information Sheet. Title of Study:
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How to fill out consent and assent form
How to fill out consent and assent form
01
Read the instructions and guidelines provided with the consent and assent form.
02
Fill out the personal information section, including the participant's name, age, and contact details.
03
Understand the purpose of the study or research project and the implications of participating.
04
Review the risks and benefits associated with participation.
05
Provide consent or assent by signing and dating the form.
06
If necessary, have a witness sign the form as well.
07
Return the completed form to the designated person or organization.
Who needs consent and assent form?
01
Consent and assent forms are needed for individuals who are participating in a study, research project, clinical trial, or any activity that involves data collection or human subjects.
02
This includes participants of all ages, including adults, minors, and vulnerable populations.
03
Consent is typically required from adults or legal guardians of minors, while assent is obtained from minors themselves to ensure their understanding and agreement to participate.
04
The forms are necessary to protect the rights and well-being of participants, establish voluntary participation, and ensure informed decision-making.
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What is consent and assent form?
Consent and assent form is a document that ensures an individual voluntarily agrees to participate in a research study.
Who is required to file consent and assent form?
Researchers conducting studies involving human subjects are required to file consent and assent forms.
How to fill out consent and assent form?
The form must be filled out by clearly explaining the purpose of the study, potential risks, benefits, and ensuring the individual understands their rights.
What is the purpose of consent and assent form?
The purpose of the form is to protect the rights and well-being of research participants by ensuring informed consent is obtained.
What information must be reported on consent and assent form?
The form must include study details, risks and benefits, participant rights, contact information, and signature lines.
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