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Trial planning

Trial feasibility assessment

The goal of a clinical trial feasibility assessment is to evaluate the feasibility of a clinical trial and the likelihood of its success. This assessment ensures that a clinical trial can be conducted effectively and efficiently.

Clinical trial feasibility assesses factors such as the availability of suitable participants, the research site's capability, the research team's expertise, regulatory requirements, budget, and timelines. It is essential to ensure the trial can be conducted effectively, efficiently, and successfully, minimising risks and maximising the potential for meaningful results.

Consumer groups/ representatives should be engaged with early in the development of the research proposal and if the project progresses be invited to be part of the research team.

Checklist of items: 

  • identify the elements of how your study will be conducted and consider potential risks, resources, budget and time factors
  • identify consumer groups/representatives to check the feasibility of the trial from the participants’ perspective
  • identify, if required, alternative solutions or approaches
  • evaluate, if required, the alternative solutions and approaches
  • produce a short feasibility report to summarise if the clinical trial is feasible.
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