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POSITION STATEMENT INFORMED CONSENT ADULTS WITH CAPACITY, ADULTS WITH IMPAIRED CAPACITY OR LACKING CAPACITY AND MINOR/MATURE MINORS Position Alberta Health Services created and approved Consent to
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How to fill out informed consent - adults?

01
Begin by reading through the informed consent document carefully. Make sure you understand all the information and requirements outlined in the document.
02
Provide your full name and any other personal information required, such as your date of birth and contact details. This is important for identification purposes.
03
If applicable, indicate whether you have any pre-existing medical conditions or allergies that could affect the study or procedure outlined in the informed consent form.
04
Take note of any potential risks and benefits associated with participating in the study or procedure. Ensure that you fully understand these risks and benefits before proceeding.
05
Review any alternative options available to you and make an informed decision about whether or not to consent to the study or procedure.
06
If you have any questions or concerns about the information provided in the informed consent form, seek clarification from the relevant healthcare professional or researcher.
07
Once you have carefully read and understood the informed consent form, sign and date it to indicate your informed consent.

Who needs informed consent - adults?

01
Informed consent is required for any adult individual who is participating in a research study or medical procedure that involves potential risks or benefits.
02
It is essential for adults to provide their informed consent as it ensures that they have been adequately informed about the study or procedure, understand the potential risks and benefits, and have the autonomy to make their own decision regarding participation.
03
Informed consent protects the rights and well-being of adults, ensuring that they are fully aware of what they are agreeing to and have the opportunity to ask questions or express any concerns before making a decision.
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Informed consent for adults refers to the process by which a competent adult willingly agrees to participate in a research study or medical treatment after being informed of all relevant aspects.
Researchers, healthcare providers, or institutions conducting the study or providing the treatment are required to obtain informed consent from adults participating.
To fill out informed consent for adults, the document should include information about the study or treatment, risks and benefits, confidentiality, voluntariness, and contact information for questions or concerns.
The purpose of informed consent for adults is to ensure that individuals have all the necessary information to make an informed decision about participating in a study or treatment.
Informed consent for adults must include details about the study or treatment, risks and benefits, confidentiality measures, voluntariness, contact information, and the right to withdraw consent at any time.
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