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This informed consent form provides essential information about a research study aimed at evaluating the effectiveness of an online screening tool designed to assist children in recovering from illness or injury. The study involves participants engaging with a gaming application while providing feedback on their feelings and symptoms over a period of 12 weeks.
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How to fill out informed consent form and

01
Read the informed consent form carefully before filling it out.
02
Provide your personal information as required, such as your name, address, and contact details.
03
Understand the purpose of the study or procedure, including potential risks and benefits.
04
Ask any questions regarding the study or the consent form to ensure clarity.
05
Indicate your willingness to participate by signing and dating the form.
06
Keep a copy of the signed form for your records.

Who needs informed consent form and?

01
Participants in medical research studies.
02
Patients undergoing medical procedures or treatments.
03
Individuals involved in psychological or behavioral research.
04
Any setting where informed consent is legally required before participation.
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An informed consent form is a document that provides potential participants of a study with detailed information about the research, ensuring that they understand the purpose, procedures, risks, and benefits before agreeing to participate.
Researchers conducting studies involving human participants are required to file an informed consent form to ensure ethical standards are maintained.
To fill out an informed consent form, researchers must provide clear information about the study, including its purpose, duration, procedures, risks, benefits, and confidentiality terms, followed by obtaining the participant's signature.
The purpose of an informed consent form is to inform potential participants about the study, enabling them to make an educated decision about their involvement and to protect their autonomy and rights.
The informed consent form must include the study's purpose, duration, procedures, potential risks and benefits, confidentiality assurances, and contact information for questions.
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