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IRISH # 19661: A descriptive observational pilot study comparing regional distribution of ventilation during lung expansion therapy in healthy human subjectsIRBHSR PROTOCOL Investigator Agreement BY
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How to fill out irb-hsr protocol

01
To fill out the IRB-HSR protocol, follow these steps:
02
Begin with the title of the study and provide a brief description.
03
Include the research objectives and aims.
04
Provide a background and rationale for the study.
05
Clearly describe the methodology and study design.
06
Identify the study population and include inclusion and exclusion criteria.
07
Outline the procedures and interventions that will be implemented.
08
Detail the data collection and analysis methods.
09
Discuss any potential risks and benefits for participants.
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Include information on informed consent procedures.
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Provide a plan for participant recruitment and retention.
12
Address confidentiality and privacy concerns.
13
Mention any conflicts of interest.
14
Include a timeline for the study.
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Provide information on funding sources, if applicable.
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Finally, review and revise the protocol before submission to the IRB.

Who needs irb-hsr protocol?

01
The IRB-HSR protocol is needed by researchers and institutions conducting human subjects research.
02
This protocol ensures that the rights and welfare of research participants are protected.
03
Institutional Review Boards (IRBs) require researchers to submit a protocol for review and approval before conducting the study.
04
The protocol is necessary to demonstrate that the research methodology is ethical and compliant with regulatory guidelines.
05
Researchers conducting biomedical, behavioral, or social science research involving human participants need to complete an IRB-HSR protocol.
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The IRB-HSR protocol refers to the Institutional Review Board - Human Subjects Research protocol, which is a document outlining the details of a research study involving human subjects.
Researchers conducting studies involving human subjects are required to file an IRB-HSR protocol.
The IRB-HSR protocol can be filled out by providing detailed information about the research study, including the study aims, methodology, recruitment methods, risks and benefits, and informed consent procedures.
The purpose of the IRB-HSR protocol is to ensure that research involving human subjects is conducted ethically and in compliance with regulations to protect the rights and welfare of participants.
The IRB-HSR protocol must include details such as the study objectives, methodology, participant recruitment methods, risks and benefits, informed consent procedures, and plans for data management and confidentiality.
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