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Informed Consent Fertile: Cluster Randomized Controlled Trial: Efficacy of Gravid Opposition Sticky Trap (GO) and Dengue NS1 Antigen Rapid Diagnostic Test for Early Surveillance of Dengue Among Adult
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Start by reading through the informed consent form carefully.
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Make sure you understand all the information provided in the form.
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Fill out your personal details such as your name, address, date of birth, and contact information.
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Write down the purpose of the study or research that the informed consent is for.
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Indicate whether you agree to participate in the study or research by checking the appropriate box.
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If there are any risks or potential side effects mentioned in the form, make note of them.
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Sign and date the informed consent form to acknowledge that you have read and understood it.
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If needed, you may also have to have a witness sign the form to validate the consent.
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Anyone who is planning to participate in a study or research that requires informed consent needs an informed consent form.
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The title of the informed consent form typically includes the name of the study or research project.
Researchers, healthcare providers, or individuals conducting a study or research project are required to file the informed consent form.
The informed consent form title can be filled out by providing the name of the study or research project in the designated space.
The purpose of including a title on the informed consent form is to clearly identify the study or research project to participants.
The informed consent form title should include the name of the study or research project, and any relevant identifying information.
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