Tailored Patient-centric Solutions to Maximize Clinical Trial Recruitment & Retention

Electronic Clinical Outcome Assessments (eCOA) simplify the collection of patient, clinician, and caregiver data while improving participant convenience, compliance, and data quality. Allucent delivers integrated, secure eCOA solutions that provide reliable, real-time data to support efficient decentralized clinical trial execution.

Telehealth and home health services enable clinical trials to reach participants wherever they are, reducing the burden of participation while maintaining the human connection between patients and care teams. Through trusted strategic partners, we deliver virtual visits and in-home clinical services that make participation easier for patients and their families, improve access to care, and support long-term engagement throughout the study.

Thanks to state-of-the-art technology, data capture is streamlined across sites, remote settings, telehealth visits, and connected devices. Real-time clinical trial performance data, together with predictive insights into enrollment, retention, and study completion, are delivered through an integrated dashboard to support faster, more informed decision-making.

Wearables and medical devices further extend this connected ecosystem by enabling participants to capture data seamlessly from home. Easy-to-use technologies improve the participant experience while supporting robust, high-quality data collection for exploratory, secondary, and even primary endpoints.

Compliant eConsent and integrated patient education provide a secure, convenient, and engaging participant experience. Participants can electronically review and sign consent forms, access study materials and instructional videos, and receive guidance for at-home activities such as IMP administration and sample collection. Integrated eDiary tracking supports protocol compliance while meeting local regulatory requirements.

Manage patient interactions throughout the trial through direct notifications and reminders ensuring participants are well-informed, engaged, and compliant with the trial requirements, which in turn supports the trial’s success. By raising site notifications based upon correct triggers, sites are directed to support those participants that require guidance and ensure all data is collected as required for the trial.

We partner with trusted providers to deliver IMP, test kits, and other clinical supplies directly to participants homes. Direct-to-patient logistics reduce the need for site visits, improve participant convenience, support protocol adherence, and help keep studies on track through coordinated communication with both participants and sites.