Sponsors can rely on Real World Evidence (RWE) to understand the target patient base and patient behavior to prepare the Patient Persona Document. This document should include demographics such as age, gender, location, education level, and occupation followed by relevant psychographic details like interests, preferences, values, attitudes, behaviors, and idea of their healthcare journey challenges and obstacles. This document also covers the patient’s medical history, previous symptoms, experience with treatments, and other relevant background information that is required to understand the patient’s needs, values, and motivations. Along with this, ensure to train each member of your team on patient personas and develop a comprehensive training document which contains all the insights.
Interview or survey potential patients, utilizing online patient forums and communities, social listening, and other reputable sources. Additionally, consult with Healthcare Providers (HCPs) and gather data from reputable online sources, advocacy groups, and investigators in the therapeutic area. Patient registries managed by advocacy groups are also a rich database of participants when looking for clinical trials as they have already reported their disease conditions, which reduces the time required to determine the inclusion criteria.
Develop clear and patient-friendly content across the channels that comply with the local and international regulations for patient recruitment for clinical trials. Leverage the expertise of patient advocacy groups and HCPs to prepare patient-friendly material in multiple languages to improve balanced representation of participants.