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Appendix I Informed Consent Form Study name Comparison of Laparoscopic With Open Distal Gastrectomy in Advanced Gastric Cancer After Neoadjuvant Chemotherapy Protocol version2.0, 2015 February 26 Informed

How to fill out appendix i informed consent

How to fill out appendix i informed consent

1. Begin by reading and understanding the purpose and the content of the informed consent form.
2. Gather all necessary information, documents, and materials that are required to complete the appendix I informed consent form.
3. Start by filling out the basic personal details of the participant, such as their name, age, gender, and contact information.
4. Clearly explain the nature of the research study or medical procedure for which the informed consent is being obtained.
5. Provide a detailed description of the potential risks, benefits, and alternatives involved in participating in the study or procedure.
6. Include any additional information or disclosures that are necessary for the participant to make an informed decision.
7. Make sure to emphasize the voluntary nature of participation and the participant's right to withdraw their consent at any time.
8. Include a section for the participant to indicate their agreement or disagreement with the informed consent by signing and dating the form.
9. Review the completed form to ensure accuracy and completeness.
10. Provide a copy of the signed informed consent form to the participant and retain a copy for your records.

Who needs appendix i informed consent?

1. Appendix I informed consent is needed by researchers, medical professionals, and institutions conducting research studies or medical procedures involving human participants. It is necessary to obtain informed consent from individuals who are being recruited or participating in these activities to ensure they are aware of the purpose, risks, benefits, and alternatives involved and can make an informed decision about their participation.

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What is appendix i informed consent?

Appendix I informed consent is a document that outlines the information provided to participants in a research study, including the risks and benefits, and the procedures involved in the study.

Who is required to file appendix i informed consent?

Researchers conducting a research study involving human participants are required to file appendix I informed consent.

How to fill out appendix i informed consent?

Appendix I informed consent is typically filled out by researchers with the help of an institutional review board (IRB) or ethics committee.

What is the purpose of appendix i informed consent?

The purpose of appendix I informed consent is to ensure that participants are fully informed about the research study and can make an informed decision about participating.

What information must be reported on appendix i informed consent?

Information such as the purpose of the study, procedures involved, risks and benefits, confidentiality, voluntary participation, and contact information must be reported on appendix I informed consent.