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VCU IRB PROTOCOL NUMBER: [HM20013532]RESEARCH PARTICIPANT INFORMATION AND CONSENT FORM STUDY TITLE: Stress and Feeding: A Pilot Intervention for Mothers and Their Preterm Infants VCU INVESTIGATOR:
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01
Begin by reviewing the guidelines provided by the relevant ethics committee or institutional review board.
02
Collect all necessary information about the research project including objectives, methodology, and participant details.
03
Outline the recruitment process for participants, ensuring fairness and clarity.
04
Detail the steps for obtaining informed consent, including how and when it will be obtained.
05
Describe the measures in place to protect the privacy and confidentiality of participants' data.
06
Specify the potential risks and benefits associated with the participation in the research.
07
Include any monitoring plans for ongoing review of the study's conduct and participant well-being.
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Submit the completed conduct of human subjects form to the appropriate review body.

Who needs conduct of human subjects?

01
Researchers conducting studies involving human participants.
02
Institutional review boards (IRBs) that oversee ethical standards in research.
03
Organizations requiring compliance with federal regulations on human subject research.
04
Anyone seeking funding for research that involves human subjects.
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Conduct of human subjects refers to the ethical and regulatory framework guiding the involvement of human participants in research. It ensures the safety, rights, and welfare of participants are protected throughout the research process.
Researchers and institutions conducting studies involving human participants are required to file conduct of human subjects. This includes academic researchers, medical professionals, and organizations involved in clinical trials.
To fill out conduct of human subjects, researchers must provide detailed information about the study protocol, participant recruitment methods, informed consent processes, and measures taken to protect participant confidentiality and safety.
The purpose of conduct of human subjects is to ensure ethical standards are upheld in research involving human participants, safeguarding their rights and welfare, and ensuring that research contributes positively to knowledge and public health.
Information that must be reported includes study objectives, methodology, participant demographics, informed consent procedures, any potential risks, and how confidentiality will be maintained.
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