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Saint Joseph's University: Human Subjects Research Protocol Application INSTITUTIONAL REVIEW BOARD FOR THE PROTECTION OF HUMAN SUBJECTS IN RESEARCH All questions must be answered and typed. All attachments

How to fill out human subjects research protocol

How to fill out a human subjects research protocol:

1. Begin by clearly defining the research question or objective of your study. This will serve as the foundation for the protocol.
2. Identify the target population or participants for your research. Specify any inclusion or exclusion criteria to ensure the selection process is appropriate.
3. Determine the sample size needed for your study and justify your decision based on statistical considerations.
4. Develop a detailed plan for data collection. Outline the methods, instruments, and procedures you will employ to gather information from human subjects.
5. Describe the potential risks and benefits associated with participating in your research. Assess and mitigate any potential harm to the participants.
6. Provide informed consent forms and processes that ensure participants fully understand the nature and purpose of the study, as well as any potential risks or benefits involved.
7. Include a section addressing the confidentiality and privacy of participants' data. Outline how you will protect their information and ensure their anonymity.
8. Discuss any potential conflicts of interest or ethical considerations related to your research. Be transparent and address any biases that could affect the integrity of the study.
9. Create a timeline for the research project, including key milestones and deadlines for data collection, analysis, and reporting.
10. Finally, submit the completed human subjects research protocol to the relevant institutional review board (IRB) or ethical committee for review and approval.

Who needs a human subjects research protocol?

1. Researchers in various fields such as medicine, psychology, sociology, and others who conduct studies involving human participants.
2. Academic institutions, universities, and research organizations that require adherence to ethical guidelines and regulations.
3. Funding agencies and grants providers that necessitate the submission of a research protocol to evaluate the scientific merit and ethical aspects of the proposed study.

For pdfFiller’s FAQs

What is human subjects research protocol?

A human subjects research protocol is a detailed plan that outlines the methodology and objectives of a research study involving human participants.

Who is required to file human subjects research protocol?

Researchers or institutions conducting research involving human subjects are required to file a human subjects research protocol.

How to fill out human subjects research protocol?

To fill out a human subjects research protocol, one must provide information on the study design, participant recruitment, informed consent process, data collection procedures, and potential risks and benefits associated with the research.

What is the purpose of human subjects research protocol?

The purpose of a human subjects research protocol is to ensure the protection of human participants involved in the research study and to maintain ethical standards.

What information must be reported on human subjects research protocol?

A human subjects research protocol should include details about the study objectives, methodology, participant demographics, informed consent process, data collection and analysis methods, and any potential risks or benefits to the participants.

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