Platform

Accelerated Clinical Trials are the modern-day singularity of health hope.

We combine a robust, innovative technology platform with highly trained professionals to deliver complete assessment data whenever, wherever, and however the trial and patients require.

Technology that goes beyond brick and mortar.

A comprehensive solution that surpasses the virtual experience — delivering real-time, validated, and highly accurate clinical data from multiple sources.

The ACT™ platform provides four key components to manage the clinical trial journey among researchers, clinicians, and trial participants:

Accelerates enrollment and reaches patients wherever they are by accessing a broad global network of clinical investigators and Hawthorne Heroes to navigate the participants through their study visit journey.

  • Automated recruiting and onboarding
  • Intelligent search and hero matching
  • Full learning management system
  • Qualification tracking for delegation of authority

Enables comprehensive screenings and longitudinal follow-up, increasing a patient’s ability to fully and thoroughly participate. Hawthorne Heroes can administer a range of highly complex in-home assessments and optimize responsiveness to protocol demands.

  • Visit scheduling and orchestration
  • Device integration including, but not limited to, wearables, EKG, Echo
  • Equipment logistics
  • Multi-model assessments: in-home, brick-and-mortar sites, telehealth

Ensures diverse participant populations and supports broader patient access to trials. The Hawthorne Effect ACT™ platform integrates with existing recruiting platforms, facilitates virtual enrollments, and provides both a centralized view of enrollment statistics and a unified patient experience.

  • Management of recruiting campaigns
  • Patient enrollment and screening
  • eConsent and ePRO
  • Recruiting and enrollment statistics

Facilitates data collection, verification, and distribution, providing the highest-quality evidence. In today’s evolving ecosystem of multi-model and highly complex visits, providing a seamless experience for the clinician and patient is key to collecting high-quality clinical evidence and accelerating data delivery for FDA or publication.

  • Virtual site management
  • Part 11-compliant eSource
  • Real-time data verification and query management
  • Seamless data integration

See firsthand how our ACT™ solution can accelerate your trials.