Step 5:
Un ensayo clínico es tan valioso como la fiabilidad de sus resultados. Los expertos en DCT de ObvioHealth saben cómo diseñar un ensayo para reclutar y capacitar a la cohorte óptima y eliminar el «ruido» estadístico, de modo que puedas obtener las pruebas sólidas que necesitas.
All captured data—whether from participants, devices, or caregivers—flows directly into ObvioGo for centralized monitoring, faster analysis, and stronger compliance. Live dashboards and automated alerts enable study teams to monitor safety, track protocol adherence, and intervene quickly when needed.
Traditional, site-based data collection is often slowed by “white coat bias,” delayed entries, and missed moments. ObvioGo overcomes these challenges by empowering participants to capture data in real time—from home or on the go—ensuring richer, more accurate datasets without added burden.
ObvioGo doesn’t just collect clinical trial data—it actively monitors it, detecting risks and triggering alerts before issues escalate. Our intelligent platform empowers study teams with real-time oversight and rapid responsiveness to keep participants safe and trials compliant.
ObvioGo’s platform integrates with medical-grade and consumer wearables, while our ecosystem of clinical and technical experts can help ensure the right device fit for your protocol.
Proper device selection is essential to ensuring consistent data capture. So, choosing the right device for your protocol should be a priority.
Capturing a range of symptoms in real time.