Guide to ePRO, clinRO, obsRO, and perfRO in Clinical Trials Info

The Ultimate Guide to ePRO, clinRO, obsRO, and perfRO in Clinical Trials

When we talk about the tools that are revolutionising clinical trials, it's impossible not to bring up ePRO, clinRO, obsRO, and perfRO.

If you’re in the world of clinical trials, you know data accuracy, compliance, and patient engagement are the foundation of reliable research.

Today, we're diving into how these powerful outcome assessment tools are making an impact, and how STK Life stands out as a partner in driving these innovations forward with the best eCOA devices.

Why Are ePRO, clinRO, obsRO, and perfRO Important for Clinical Trials?

Clinical trials rely on solid data.

You need information that’s consistent, real-time, and clear from every angle—whether that’s from the patient, the clinician, or even a caregiver.

Each type of outcome assessment plays a unique role in collecting data, enhancing the quality of your research, and ultimately, improving patient care.

With STK Life’s eCOA devices, you’re equipped to tackle these requirements with tools that are simple, customisable, and efficient.

Let’s break down what each outcome assessment does and how STK Life is transforming the process.

1. What is ePRO, and Why Does It Matter?

ePRO, or Electronic Patient-Reported Outcomes, allows patients to report their own health information in real-time.

In traditional trials, patients might write down their symptoms or experiences on paper.

But with ePRO devices from STK Life, patients can input their information right into an easy-to-use, secure interface on a smartphone or tablet.

This isn’t just convenient—it’s critical for accuracy.

STK Life’s ePRO devices are user-friendly and support compliance with global regulatory standards.

And if you’re managing a decentralised trial, these tools are ready to deploy across various locations without a hitch.

Here’s why STK Life ePRO devices work so well in clinical trials:

  • User-friendly interface: Patients don’t need to be tech experts; it’s all about accessibility.
  • Global compatibility: STK Life’s devices are certified for use in over 80 countries, making them ideal for large-scale, multi-site trials.
  • Reliable performance: With a 5-year warranty and long battery life, you’re assured of minimal interruptions.

2. The Role of clinRO in Clinical Trials

Next up is clinRO or Clinician-Reported Outcomes.

In some trials, clinicians need to assess a patient’s health status directly.

STK Life devices support clinRO by providing tools that make it easy for clinicians to input data during a patient visit.

It’s all digital, it’s all efficient, and it’s completely reliable.

With clinRO on STK Life devices, clinicians can document patient information during visits or even remotely with secure video options, all while staying compliant.

The key benefits?

  • Secure, direct entry: Clinicians can record findings without worrying about data loss or misinterpretation.
  • Real-time data access: Updates are instantly available, meaning faster insights for your research team.
  • Customised MDM support: STK Life customises each device, allowing remote management and updates to meet the specific needs of your trial.

3. Understanding obsRO and its Value in Trials

obsRO stands for Observer-Reported Outcomes.

This is where data comes from someone close to the patient, like a caregiver, rather than the patient or clinician.

For instance, in cases where the patient can’t self-report, such as in paediatric or geriatric trials, obsRO provides crucial insights.

STK Life’s devices make this seamless.

Caregivers can use the customised interfaces to record their observations, giving trial administrators access to honest, real-world data.

With obsRO on an STK Life eCOA device, you get:

  • Effortless data entry for caregivers: A simple, easy-to-use interface means caregivers can quickly document observations.
  • Secure connectivity: With encrypted data transfer and control over device management, you can rest assured that all information is securely stored and managed.
  • Fully compliant tech: obsRO data aligns with regulatory standards, ensuring that each observation contributes directly to the quality of the trial.

4. Why perfRO is the Key to Objective Data

perfRO, or Performance-Based Outcomes, records measurable data directly from patients, like walking distance or cognitive test results.

This is gold for researchers looking to collect objective data.

With STK Life’s robust devices, perfRO data can be captured accurately and efficiently.

Whether you’re using wearables or smartphones, STK Life devices are optimised for gathering performance data that meets rigorous compliance standards.

Here’s why STK Life is ideal for perfRO:

  • Precision in data collection: Customised sensors and software ensure that every performance metric is captured accurately.
  • Multi-functionality: STK Life’s devices are built for more than just one type of data, supporting complex trials with varied data needs.
  • Scalable tech: Ready for both BYOD (Bring Your Own Device) options or STK Life-provided devices, so you’re covered on both fronts.

How STK Life Makes a Difference in ePRO, clinRO, obsRO, and perfRO

When it comes to clinical trials, you need a partner that knows the ins and outs of tech, compliance, and ease of use.

STK Life is that partner.

With over three decades in mobile tech, STK Life has built eCOA devices that can handle everything from patient diaries to complex performance metrics.

STK Life makes devices that aren’t just durable but also globally compatible and fully compliant.

Why Choose STK Life?

  • Global reach: With offices in the UK, EU, China, and Hong Kong, STK Life has the expertise and logistical network to support clinical trials worldwide.
  • Dedicated support: STK Life offers a 5-year warranty on devices and lifetime software support, so you know they’ve got your back.
  • Customisation: From interface adjustments to MDM configuration, STK Life makes sure their devices work exactly how you need them to.
  • Regulatory compliance: Every device meets global standards, making it easier to deploy across borders without hassle.

Simple Steps for Deploying STK Life eCOA Devices in Your Trial

Getting started with STK Life’s eCOA devices is straightforward.

Here’s how:

  1. Select your device: Choose from STK smartphones, tablets, or wearables.
  2. Customise software and MDM: STK Life’s team works with you to customise each device.
  3. Set up the user experience: Tailor the onboarding process to make it easy for participants.
  4. Global testing: Devices are tested for use worldwide, ensuring compliance.
  5. Software and security support: Long-term support is included, ensuring no interruptions.
  6. Certification: STK Life certifies each device under Google’s GMS program.
  7. Full compliance: All devices are fully compliant with international standards.
  8. Logistics support: From setup to delivery, STK Life ensures everything runs smoothly.

FAQs About ePRO, clinRO, obsRO, and perfRO

What is an ePRO device?

ePRO devices let patients report their health information directly, making it easy to gather data in real-time.

Why use clinRO, obsRO, and perfRO in clinical trials?

Each tool collects a unique type of data: clinRO from clinicians, obsRO from caregivers, and perfRO based on patient performance, creating a complete data set for trials.

How does STK Life support clinical trials with these devices?

STK Life provides customisable devices with global compatibility, compliance, and long-term support, making them ideal for clinical data collection.

Are STK Life devices suitable for decentralised clinical trials?

Absolutely. STK Life devices are designed for flexibility and are fully certified for use in multiple countries.

Conclusion

At the end of the day, STK Life is all about enhancing clinical trials with reliable, compliant, and easy-to-use ePRO, clinRO, obsRO, and perfRO devices.

With these tools, you’re not just gathering data—you’re transforming it into insights that drive better patient care.

Ready to elevate your clinical trial?

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