Feasibility Studies

Patient recruitment feasibility studies are conducted based on the protocol and area of sites by experienced PRCs and CRCs. High-accuracy recruitment simulation is performed based on over 10,000 per year enrollment performance data and the patient volunteer database that we hold. In addition, database patient research and protocol design support can be implemented. Research on patients is performed to define the ideal subject profile for the protocol.

Collecting the voices of patients and their family members in order to clarify the target patient profile. This is done by conducting questionnaires and interviews (quantitative/qualitative research) to volunteer database members. A better patient recruitment strategy can be formed by using this data. In addition, conducting this research while designing the protocol will help protocol development by incorporating patient insight.

Our patient recruitment planning includes not only site selection and recruitment methods, but also other aspects such as promoting patient understanding of clinical trials and improving their motivations (preventing them from dropping out from the study). Understanding the patient is one of the most important aspects to a clinical trial. We propose high accuracy recruitment strategies that best fit the protocol based on patient insight research and past achievement.