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Step 5:

Data Capture & Monitoring

Smarter Data. Safer Studies. Stronger Evidence.

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.

Real-Time, Real-World Data Collection

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.

91%

ePRO Compliance

89%

Retention
Average rates for ObvioHealth completed studies.
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Selección y validación de instrumentos

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.

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Seleccione los instrumentos óptimos

Identificamos los instrumentos, dispositivos y dispositivos portátiles que son más apropiados para la población, la afección y el tratamiento en estudio.
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Augmented ePRO

Captures outcomes in real-world settings—enhancing traditional ePRO with features like automatic image optimization, acoustic data capture (e.g., cries, coughs, speech), and AI-enabled flagging to improve accuracy and reliability.
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Evalúe las ventajas y desventajas

Arbitramos entre la reducción de la carga de los pacientes y la calidad de los resultados, teniendo en cuenta la fatiga, la usabilidad y la granularidad de los datos.
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Multimedia Capture

AI-assisted image, video, and audio capture capabilities make it easier for participants or their caregivers to record and submit the required outcome with just a couple of taps on their mobile devices.
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Sensors & Wearables

Break down geographic and access barriers. ObvioGo supports seamless integration with medical-grade devices, enabling passive data capture from more diverse and representative populations in real-world settings.
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Unified, Intelligent Platform

All data streams—ePRO, eCOA, multimedia, wearables—flow directly into the ObvioGo platform for live monitoring, automated alerts, and rapid decision-making.

Monitoring that Mitigates Risk

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.

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Real-Time Dashboards

Dynamic, AI-powered dashboards give sponsors and sites real-time visibility into trial progress, safety, and protocol adherence—all at a glance.
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Automated Alerts

Automated alerts are triggered by missed activities, outlier data, or potential adverse events, allowing teams to intervene proactively.
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Rapid AE Identification & Response

ObvioGo enables near-instantaneous AE and SAE recognition through built-in monitoring and virtual team response—minimizing risk and supporting regulatory compliance.
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Remote Oversight

Virtual oversight tools reduce the need for in-person visits, while keeping project managers and investigators informed in near real time—enhancing both safety and operational efficiency.
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Device Integration to Support Your Endpoints

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.

Device Selection

Evaluated by experts and designed for your trial.

Seamless Integration

Our product team ensures that all device data flows directly to the EDC, patient app screen, or other appropriate destination.

Data Management

Real-time data transfer enables more rapid and informed decision-making.

Careful Device Selection for More Meaningful Outcomes

Proper device selection is essential to ensuring consistent data capture. So, choosing the right device for your protocol should be a priority.

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Relevance

Appropriateness for protocol and disease state.
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Usability

Comfort, ease of use, and frequency of capture.
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Reliability

Reproducibility of the measurement.
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Validity

Proper measurement of the underlying trait of interest.
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Safety

Ability of the measurement to rapidly signal any health risks.
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Privacy

Encryption of data.

Integrate with Consumer Wearables and Medical-Grade Sensors

Capturing a range of symptoms in real time.

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Respiratory rate at rest

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Heart rate

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Heart rhythm

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6-Lead EKG

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Blood oxygen level

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Pulse rate

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Perfusion index

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Blood pressure

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Skin temperature

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Steps and activity level

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Body position

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Sleep status

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Fall detection

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Gait analysis

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Cough episodes

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Weight/BMI

Key Benefits of Wearables and Sensors Integration

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Early Detection of AE's

Symptoms can fluctuate from week to week or even hour to hour. Sensors and wearables enable more frequent measurement, so study teams can quickly identify AEs or SAEs that otherwise might be missed.
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More Inclusive Trials

In cohorts that include vulnerable populations such as the elderly or those with chronic disease, reduced mobility, or stigmatized diseases, user-friendly devices can increase the likelihood of participation.
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Increased Patient Compliance

When patients share their data from home—either actively or passively—their participation in a trial is less fatiguing. This ease makes it more likely that patients will remain in the study until the end.
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Faster Insights

Access real-time data streams and centralized dashboards that accelerate decision-making and keep your trial on track from day one.
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Improved Accuracy

Sensors and wearables can complement or replace certain ePRO elements, delivering more and richer real-time data points. They also provide better objectivity, reducing bias.
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Stronger Retention

Participant-friendly tools improve the trial experience, making it easier for patients to stay engaged and complete the study.
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Making Real Impact