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This document provides guidelines for preparing research proposals to be submitted to the Neumann University Institutional Review Board (IRB), outlining required sections, the submission process,
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How to fill out Guidelines for the Preparation of Research Proposals for IRB Review

01
Read the IRB guidelines thoroughly to understand the requirements.
02
Identify the type of research you are proposing and ensure it falls under IRB oversight.
03
Prepare a clear and concise research proposal including objectives, methods, and expected outcomes.
04
Include information on participant recruitment, informed consent process, and data collection methods.
05
Address potential risks to participants and how you plan to mitigate them.
06
Clearly state how you will protect participant confidentiality and data security.
07
Outline the timeline and budget for your research project.
08
Review your proposal to ensure it is complete and adheres to the IRB's formatting guidelines.
09
Submit the completed proposal along with any required supplementary documents to the IRB for review.

Who needs Guidelines for the Preparation of Research Proposals for IRB Review?

01
Researchers conducting studies involving human participants.
02
Students preparing research projects for academic purposes.
03
Institutional staff involved in the review of research proposals.
04
Any individual or organization seeking ethical approval for research activities.
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What should it include? Project title. Your title should clearly indicate what your proposed research is about. Research supervisor. Proposed mode of research. Aims and objectives. Synopsis. Background. Expected research contribution. Proposed methodology.
IRB review and approval is required for projects that: Meet the definition of research. Involve human subjects and. Include any interaction or intervention with human subjects or involve access to identifiable private information.
All proposals submitted for either expedited or full review must contain four primary sections: Purpose of investigation and procedures. Anticipated risk and potential benefits to participants. Steps taken to protect the participants. Manner of obtaining participants.
Follow these steps to write an effective research proposal: Include a title page. Develop an abstract. Write an introduction. Include background information. Develop research questions. Compose a problem statement. Develop a literature review. Describe your research methodologies.
The quick list: Complete CITI training if you are not up to date. Prepare all your documents (consent, stimuli & materials, surveys, recruitment) beforehand. Go to your institution's IRB app site. Read carefully. Follow the instructions. Answer clearly. Don't be wordy. Whenever possible, give yourself wiggle room.
Checklists are used by the IRB staff and reviewers to document required IRB determinations. Investigators may consult the checklists to understand the regulatory requirements related to research, however, Investigators are not required to complete the checklists: HRP-410 - Waiver or Alteration of the Consent Process.
If your study is more than minimal risk, it will be harder for you to get IRB approval. You will need to justify why you are running the study. Less common types of risk for psychology studies are social, physical, and financial.
IRB – Principles Respect for Persons. Acknowledgement of the autonomy of the individual and the responsibility to provide special protection for individuals with reduced autonomy. Beneficence. A responsibility to do no harm, to maximize possible benefits, and to minimize possible harm. Justice.

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The Guidelines for the Preparation of Research Proposals for IRB Review are a set of protocols and instructions that researchers must follow to ensure that their research involving human subjects adheres to ethical standards and legal requirements.
All researchers and faculty members who plan to conduct research involving human subjects at institutions with an Institutional Review Board (IRB) are required to file these guidelines.
Researchers must complete the guidelines by providing detailed information about the study design, methodology, recruitment processes, informed consent procedures, and data handling, ensuring all ethical considerations are addressed.
The purpose is to protect the rights and welfare of human subjects by ensuring that all research proposals are evaluated for ethical compliance, methodological soundness, and potential risks.
Researchers must report information including the study's objectives, participant demographics, recruitment methods, informed consent processes, potential risks and benefits, and data confidentiality measures.
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