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Appendix. Consent Form (English Version) INFORMED CONSENT FORM This Informed Consent Form is for women 18 years of age and above whom attend Irene District Hospital and receive cesarean section surgery.
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Read the sample informed consent form carefully.
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Fill in your personal information accurately, such as name, age, and contact details.
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Understand the purpose and scope of the study or procedure mentioned in the form.
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Ask any questions you have about the study or procedure before signing the form.
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If you agree to participate or give consent, sign the form.
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Who needs sample informed consent form?

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Researchers conducting studies involving human participants.
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Medical professionals obtaining consent for medical procedures.
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Any individual or organization involved in research or experiments requiring informed consent.
04
Institutions and organizations that follow ethical guidelines and protocols.
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A sample informed consent form is a document used to inform participants about the details of a study or procedure, ensuring they understand the risks, benefits, and their rights before agreeing to participate.
Researchers, institutions, or organizations conducting studies involving human participants are required to file a sample informed consent form to ensure ethical standards are met.
To fill out a sample informed consent form, provide clear information about the study's purpose, procedures, risks, benefits, confidentiality, and participant rights. Ensure participants read and understand the information before signing.
The purpose of a sample informed consent form is to obtain voluntary participation from individuals in research, ensuring they are fully aware of what participation entails and protecting their rights.
The sample informed consent form must report information such as the study's purpose, procedures, potential risks and benefits, confidentiality measures, and how to withdraw from the study.
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