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Start by outlining the goals and objectives of the study.
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Identify the target population or sample size needed for the study.
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Develop a detailed plan for data collection and analysis.
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Conduct a pilot study to test the feasibility of the study design.
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Evaluate the results of the pilot study and make any necessary revisions to the study protocol.
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Finalize the feasibility and preliminary efficacy sections of the study proposal.

Who needs feasibility and preliminary efficacy?

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Researchers and scientists who are planning to conduct a research study or clinical trial.
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Funding agencies or grant review committees who need to assess the potential impact and feasibility of a proposed study.
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Ethics committees or institutional review boards who need to ensure the safety and ethical conduct of a research study.
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Feasibility refers to the practicality and viability of a project or study, assessing whether it can be successfully carried out. Preliminary efficacy evaluates the initial effectiveness of an intervention based on early data.
Typically, researchers or organizations conducting clinical trials or studies involving new interventions are required to file feasibility and preliminary efficacy.
Filling out feasibility and preliminary efficacy forms involves gathering required data about the study design, methodology, participant recruitment, and initial results, and entering this information into the designated reporting templates or systems.
The purpose of feasibility is to determine whether a study can be conducted as planned, while preliminary efficacy aims to establish initial evidence that the intervention may be effective.
Key information includes study objectives, design, participant demographics, recruitment strategies, preliminary outcome measures, and any challenges faced during the study.
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