An effortless way to gain deeper insights
Sensors & Wearables
Collect objective data
Observe real-world behavior
Our integrated wearable/sensor technology provides valuable insights into real-world functioning for a greater understanding of treatment effects.
Drive endpoint accuracy
Data-driven notifications can remind patients failing to wear their device, leading to reductions in missing data, more complete datasets, and more reliable clinical endpoints.
Simplify use for patients & sites
Combined with eCOA, our devices simplify set-up and data collection activities
Integrate with Signant SmartSignals eCOA
BETTER PATIENT OVERSIGHT
This single platform approach simplifies data collection workflows. Investigators and sponsors can review quality-of-life and eCOA data together for an integrated, real-time review of patients’ health status.
DRIVE ENDPOINT QUALITY
It also drives endpoint quality by providing data-driven notifications and reminders to prevent missing data.
Why choose Signant SmartSignals?
Mobile health sensors and wearable devices collect valuable insights into the treatment effects beyond routine clinic visits. Our integrated wearables and mobile sensors collect objective data for endpoint studies without burdening the patients or sites.
Signant SmartSignals Sensors & Wearables will help you remotely monitor patient safety, understand real-world behavior, collect data at more frequent intervals, and conduct a virtual study.
Connected devices integrate with our SmartSignals eCOA:
Respiratory Monitors
Blood Glucose Monitors
Smart Inhalers
Sleep Monitors
Activity Monitors
Finger Pulse Oximeters
FAQs
What is an eCOA clinical trial?
An eCOA clinical trial uses technology to accelerate clinical data collection and ensure proper data quality analyses. More sponsors are choosing eCOA for their clinical trials to gain a better understanding of how patients feel and function in near real-time.
What is the difference between eCOA and ePRO?
The difference between Electronic Clinical Outcome Assessment (eCOA) and Electronic Patient-Reported Outcome (ePRO) is that ePRO systems are a type of eCOA. Clinical trial patients often use eCOA system technologies on mobile devices to remotely send their ePRO symptoms and experience directly to site staff. Other types of COA include Electronic Performance Outcome ePerfO, Electronic Clinician-Reported Outcome (eClinRO), and Electronic Observer-Reported Outcome (eObsRO).
Does Signant have an instrument library?
Signant’s instrument library contains over 50 instruments commonly used in clinical trials. In many cases, we offer pre-approved versions, which means an author review step is not required. Additionally, our library instruments are designed using best practices and are pre-validated, so they do not require additional testing when implemented in a new clinical study, saving you time and ensuring high quality.
Can you provide scientific consulting to support our eCOA approach?
Signant proudly provides expert consulting with our solutions, like eCOA. We believe that combining our advanced technology with scientific and clinical expertise properly sets studies up for success. Our focus on protecting data quality along with our credibility among authors and license holders helps us successfully navigate electronic implementations. With a deep understanding of regulatory needs, our team can help steer clients throughout their clinical trials.
Can Signant implement computerized adaptive tests (CATs)?
Yes. Signant SmartSignals eCOA includes the ability to implement the PROMIS CAT seamlessly alongside conventional PROMS. Choose from more than 20 domains including anxiety, depression, fatigue, sleep disturbance, pain interference, physical function, and social function. For more information, read our PROMIS CAT brochure and white paper.
Want to learn more?
Add eCOA to your study to collect accurate data at a larger scale – contact our team today.