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APPENDIX 14: INFORMED CONSENT Former Madam/Sir, RE: REQUESTING CONSENT FROM PARTICIPANTS IN A SURVEY: THE IMPACT OF THE IMPLEMENTATION OF ARTIFICIAL INTELLIGENCE IN THE CONSTRUCTION INDUSTRY I am
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Read the informed consent form thoroughly to understand the purpose and details of the study or procedure.
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Provide accurate and truthful information about yourself, including any relevant medical history or conditions.
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Ask any questions you may have about the form or the study before signing.
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Individuals who are participating in a research study or medical procedure that involves potential risks or benefits.
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Minors or individuals who may not have the capacity to provide informed consent on their own behalf.
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Informed consent form is a document that individuals are asked to sign to confirm that they are fully aware of the risks and benefits of a certain treatment or procedure before agreeing to it.
Healthcare providers, researchers, and medical facilities are required to have patients or participants sign informed consent forms.
Informed consent forms are typically filled out by providing the patient or participant with all necessary information about the treatment or procedure, allowing them to ask questions, and obtaining their signature to indicate understanding and agreement.
The purpose of informed consent form is to ensure that individuals are fully informed about the risks and benefits of a treatment or procedure before making a decision to proceed.
Informed consent forms must include details about the treatment or procedure, potential risks, benefits, alternative options, and the patient's right to refuse or withdraw consent.
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