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INFORMED CONSENT FORM
PROJECT TITLE: The effectiveness of occupation based, chronic disease self-management
programs on occupational participation
PRINCIPAL INVESTIGATORS: Jess Garvey and Dr Deirdre
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How to fill out informed consent form

How to fill out an informed consent form:
01
Read the form carefully: Begin by thoroughly reading the informed consent form to understand the purpose, risks, benefits, and procedures involved in the activity you are consenting to. Take note of any questions or uncertainties you may have.
02
Seek clarification: If there are any parts or terms of the form that are unclear, do not hesitate to ask questions. It is important to fully understand what you are agreeing to and the implications it may have.
03
Provide accurate personal information: Fill in your personal details accurately, including your full name, address, contact information, and any other requested information. This ensures that the consent form is properly assigned to you.
04
Consent statement: Typically, there will be a section where you need to provide your consent. This may involve checking a box, initialing, or signing. Make sure to indicate your consent in the specified manner as required by the form.
05
Date the form: Include the date of signing on the form. This helps establish when the consent was given and is important for record-keeping purposes.
06
Witness or representative signature (if applicable): In some cases, a witness or representative may be required to sign the form as well. If this is the case, ensure that the appropriate individual is present to witness your consent and signs the form accordingly.
07
Keep a copy: After signing the informed consent form, it is essential to keep a copy for your records. This can serve as your reference in case of any future queries or concerns.
Who needs an informed consent form?
01
Researchers and scientists: In the field of research, informed consent forms are typically necessary to ensure that participants understand the purpose, risks, and benefits of the study before agreeing to participate. This helps protect the rights and well-being of the individuals involved.
02
Healthcare providers and medical procedures: Before undergoing any medical procedure or treatment, healthcare providers are required to obtain informed consent from patients. This allows patients to make informed decisions about their healthcare and understand what to expect during the procedure.
03
Legal and business transactions: In certain legal and business situations, informed consent forms may be necessary. For instance, when entering into a contract or agreement, parties may be required to provide informed consent to indicate their understanding and agreement to the terms and conditions.
Overall, informed consent forms are crucial in ensuring transparency, autonomy, and protection for all parties involved in various activities.
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What is informed consent form?
Informed consent form is a document that provides information about a research study to potential participants, allowing them to make an informed decision about whether to participate.
Who is required to file informed consent form?
Researchers or organizations conducting a research study are required to file an informed consent form.
How to fill out informed consent form?
To fill out an informed consent form, participants must carefully read the information provided, ask any questions they may have, and sign the document to indicate their agreement to participate.
What is the purpose of informed consent form?
The purpose of an informed consent form is to ensure that participants understand the risks and benefits of participating in a research study, and to protect their rights and privacy.
What information must be reported on informed consent form?
An informed consent form must include details about the study purpose, procedures, risks, benefits, confidentiality measures, and contact information for questions and concerns.
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