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FOR IRB USE ONLY APPROVED BY: IRB01 IRB ID #: 201802800 APPROVAL DATE: 09/01/18 EXPIRATION DATE: 05/10/19INFORMED CONSENT DOCUMENT Project Title: A Phase II Trial of plus Highest Acerbate in Locally
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To fill out protecting human participants in, follow these steps:
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Start by providing a descriptive title for your research project.
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Indicate the type of review being conducted (e.g., exempt, expedited, full review).
04
Provide background information on the purpose of your research and the potential benefits it may offer.
05
Describe the methods and procedures you will use to ensure the safety and well-being of participants.
06
Outline any potential risks or discomfort that participants may experience and explain how you will minimize these risks.
07
Include a section on informed consent, detailing how you will obtain informed consent from participants and ensure their understanding of the study.
08
Describe the qualifications and experience of the researchers involved in the study.
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Include any additional documents or materials that support your application, such as questionnaires or consent forms.
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Review your application carefully before submitting it to ensure all necessary information is included.
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Submit your completed application to the appropriate institution or review board for consideration.
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Remember to always prioritize the well-being and rights of human participants throughout your research.

Who needs protecting human participants in?

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Anyone conducting research involving human participants needs to adhere to guidelines for protecting their rights and well-being.
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This includes researchers in various fields such as psychology, sociology, medicine, and social sciences.
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Academic institutions, hospitals, and research organizations typically have ethical review boards or institutional review boards (IRBs) that oversee and approve research involving human participants.
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These boards ensure that the research is conducted ethically, with proper informed consent, and with necessary safeguards to protect the participants.
05
Compliance with regulations for protecting human participants is a crucial aspect of any research project involving human subjects.
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Protecting human participants is in research studies.
Researchers conducting the study are required to file protecting human participants in.
Protecting human participants can be filled out by providing information on the study protocol, risk assessment, and informed consent process.
The purpose of protecting human participants is to ensure ethical treatment and safety of individuals participating in research studies.
Information on study design, risk assessment, informed consent process, and safety monitoring must be reported on protecting human participants.
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