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A-3 INSTITUTIONAL REVIEW BOARD PART I APPLICATION FOR APPROVAL TO USE HUMAN SUBJECTS IN RESEARCH Return the original and one electronic copy of the application to: Jim Belcher, IRB Chair Stark State
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Point by point guide on how to fill out IRB application - Stark:

01
Start by carefully reading the instructions: Before filling out the IRB application, it is essential to thoroughly read and understand the instructions provided. This will ensure that you provide accurate and relevant information.
02
Provide relevant project details: Begin by providing necessary project details such as the project title, research objectives, and a concise description of the study. This will help the IRB understand the purpose and scope of your research.
03
Identify the target population: Clearly specify the demographic characteristics of the participants you intend to involve in your study. This includes age range, gender, ethnicity, and any other relevant factors. It is crucial to ensure that your research is inclusive and does not discriminate against any specific group.
04
Describe the study procedures: Explain in detail the steps you will take to collect data and conduct your research. This includes information on data collection methods, the duration of the study, any potential risks or discomfort that participants may experience, and how you plan to address any ethical concerns.
05
Outline informed consent process: Describe how you will obtain informed consent from participants. This should include details on how you will inform participants about the purpose, procedures, and potential risks associated with the research. You should also provide information on how you will maintain confidentiality and protect the privacy of participants.
06
Include supporting documents: Make sure to attach any required supporting documents, such as research protocols, survey questionnaires, interview scripts, or consent forms. These documents should align with the information provided in the application and should be properly formatted for review.

Who needs an IRB application - Stark?

Researchers involved in human subjects research need an IRB (Institutional Review Board) application. The IRB ensures that research involving human participants is conducted ethically and in compliance with regulations. Therefore, any researcher planning to engage with human subjects to collect data or study human behaviors, experiences, or preferences must submit an IRB application for review and approval before commencing their research. The IRB application ensures the safety and protection of research participants, promotes ethical standards, and maintains the integrity of research outcomes.
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IRB application - STARK (Strengthening Transparency in Assessement of Risk) is a tool used to assess and manage research risk.
Researchers conducting studies involving human subjects are required to file an IRB application - STARK.
To fill out an IRB application - STARK, researchers need to provide detailed information about their study design, potential risks to participants, and how they plan to mitigate those risks.
The purpose of the IRB application - STARK is to ensure that research involving human subjects is conducted ethically and with proper risk management in place.
Information such as study objectives, participant demographics, informed consent procedures, and risk assessment must be reported on an IRB application - STARK.
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