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RESEARCH IN PROGRESS P E E R R E V I E W E DDesign of a randomized trial of a multidisciplinary intervention for knee osteoarthritis: Pharmacist Initiated Intervention Trial in Osteoarthritis (Photo)
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How to fill out feasibility of a randomised

01
Define the research question or hypothesis for the randomised study.
02
Determine the target population or sample size for the study.
03
Assess the availability of resources such as funding, personnel, and data for the study.
04
Consider ethical and regulatory considerations for conducting a randomised study.
05
Evaluate the potential risks and benefits of the study for participants and stakeholders.

Who needs feasibility of a randomised?

01
Researchers who are planning to conduct a randomised study to evaluate the effectiveness of an intervention or treatment.
02
Funding agencies or grant providers who require evidence of feasibility before committing resources to a randomised study.
03
Institutional review boards or ethics committees responsible for ensuring the ethical conduct of research studies involving human subjects.
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Feasibility of a randomised refers to the likelihood or possibility of conducting a randomized study successfully.
Researchers or organizations planning to conduct a randomized study are required to file feasibility of a randomised.
Feasibility of a randomised can be filled out by providing detailed information on the study design, sample size, recruitment methods, and data analysis plan.
The purpose of feasibility of a randomised is to assess the practicality and potential success of conducting a randomized study.
Information such as study objectives, study population, inclusion/exclusion criteria, potential challenges, and resources needed must be reported on feasibility of a randomised.
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