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Research Protocol Template (source of this template is unknown;modified by the UT HSC IRB)Helpful hints: If you are new to research here, consult the UT HSC IRS webpage Getting Started (http://www.uthsc.edu/research/compliance/irb/researchers/gettingstarted.php)
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How to fill out protection of human subjects

01
Identify the purpose of the research study and determine if it involves human subjects.
02
Obtain informed consent from the participants by providing them with all relevant information about the study, including potential risks and benefits.
03
Protect the privacy and confidentiality of the participants by using appropriate measures to ensure that personal information is kept secure.
04
Minimize any potential harm to the participants by designing the study in a way that reduces risks and ensures the well-being of the participants.
05
Obtain approval from an Institutional Review Board (IRB) or similar ethics committee before conducting the study.
06
Continuously monitor the study to ensure that the rights and welfare of the participants are being protected.
07
Communicate any changes to the study protocol or potential risks to the participants and obtain their consent if necessary.
08
Report any adverse events or violations of ethical guidelines to the appropriate authorities.
09
Keep accurate and detailed records of the study, including participant demographics and any interactions or interventions.
10
Finally, analyze the data collected in an ethical and responsible manner, ensuring that participants' identity and confidentiality are maintained.

Who needs protection of human subjects?

01
Researchers and scientists who conduct studies involving human participants need to ensure the protection of human subjects.
02
Institutions such as universities, research organizations, and medical facilities also have a responsibility to safeguard the rights and welfare of human subjects.
03
Ethics committees and Institutional Review Boards (IRBs) play a crucial role in reviewing and approving research studies to ensure the protection of human subjects.
04
Government agencies and regulatory bodies may also require researchers to follow guidelines and regulations for the protection of human subjects.

What is Protection of Human Subjects in ResearchHomework ... Form?

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Protection of human subjects refers to the ethical and legal measures implemented to safeguard individuals participating in research studies from potential harm, ensuring their rights, welfare, and dignity are respected.
Researchers conducting studies involving human subjects, as well as institutions that receive federal funding for such research, are required to file for protection of human subjects.
To fill out protection of human subjects, researchers must submit a research proposal to an Institutional Review Board (IRB) that includes details about the study's purpose, methodology, participant recruitment, informed consent process, and risks involved.
The purpose of protection of human subjects is to ensure that research conducted involving human participants is ethical, minimizes risk of harm, and respects the autonomy and rights of participants.
Information that must be reported includes the study's objectives, recruitment methods, informed consent procedures, risk assessment, and the measures taken to ensure participant confidentiality and safety.
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