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INFORMED CONSENT FOR PARTICIPATION AT CAMPUS ACTIVITIES On 22/09/2015 St. JohnsRavenscourt School has arranged the following activity: Grade 11 Canadian History Historical Thinking Walking Tour THIS
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Start by reading the informed consent form thoroughly to understand the purpose and expectations of the study or activity you will be participating in.
02
Fill out your personal information accurately and completely, including your full name, contact details, and any relevant medical history or conditions that may affect your participation.
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Review the risks and benefits section carefully, ensuring that you understand all potential drawbacks and advantages of taking part in the study or activity. If you have any concerns or questions, seek clarification from the researcher or organizer.
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Consider the confidentiality and data protection measures outlined in the consent form. Ensure that you are comfortable with the level of privacy and security provided for your personal information.
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Read and comprehend any terms of compensation or reimbursement mentioned in the form. Make sure you are aware of what you are entitled to receive, if applicable.
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If the consent form includes a section for voluntary participation, carefully consider whether you are comfortable participating without any external pressure or coercion.
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Sign and date the informed consent form, indicating your agreement to participate voluntarily. Some forms may require a witness, so ensure that all necessary signatures are provided.

Who needs informed consent for participation?

Informed consent should be obtained from anyone who will be participating in a study, research project, clinical trial, or any activity that involves the collection of data, observation, or experimentation on human subjects. This includes individuals of all age groups, regardless of their demographic or personal characteristics. Informed consent serves to protect the rights and well-being of participants by ensuring they have a clear understanding of the study's purpose, procedures, potential risks, and benefits before they agree to participate.
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Informed consent for participation is a process in which a participant in a study or activity is provided with all relevant information about the risks and benefits involved, and voluntarily agrees to take part.
Researchers or organizers are required to obtain and file informed consent for participation from all participants before they can take part in the study or activity.
Informed consent forms are typically filled out by the participant or their legal guardian, after reading and understanding all the information provided in the form.
The purpose of informed consent for participation is to ensure that participants are fully informed about the risks and benefits of taking part in a study or activity, so they can make an informed decision about whether to participate or not.
Informed consent forms typically include information about the purpose of the study or activity, potential risks and benefits, procedures involved, confidentiality measures, and the right to withdraw from participation at any time.
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