CuePath smart stickers for blister packs enable clinical researchers to conduct large, distributed, placebo-controlled drug trials with high accuracy and timely reporting.
Ideal for controlled substance or high-value pill-based drug trials, CueStickers are currently being used in a major methamphetamine use disorder drug treatment trial across Canada to reach and retain a vulnerable, marginalized and highly-mobile study population.
CueStickers connect easily to common Clinical Trials Management Software including RedCap. No identifying patient information passes through CuePath servers to ensure study data security and integrity.
Our Core Values
Safety
Communicates our commitment to protecting users
Adherence
Implies reliability and consistency in our approach
Dignity
Conveys respect and personalized care for every individual
Recovery
Focus on the ultimate goal: substance use disorder recovery
Revolutionizing Drug Trial Management
Precision Tools for Complex Clinical Trials
CueStickers replace the need for study participant self-reporting by providing date and time stamp collection for blister pack drugs.
Designed initially for addiction and pain management studies, these printed electronic stickers integrate seamlessly into clinical trial protocols requiring accurate medication adherence and tracking.
By providing real-time insights into participant behavior, CuePath empowers researchers to manage trial complexities effectively, ensuring the reliability of outcomes and regulatory compliance.
Key features include
Enhanced Adherence Monitoring
Automatically records when each blister is opened, delivering precise data on medication usage
Improve Recruitment & Retention
No behavior change for blister pack users, reduces clinic visits.
Scalable for Large Trials
Capable of managing trials with hundreds of distributed participants without compromising data accuracy
Streamlined Connection to Clinical Trial Management Systems
CuePath’s smart sticker technology is designed for effortless integration with existing clinical trial management software, offering unmatched customization and ease of use. Whether you’re working with proprietary systems or widely used platforms, CuePath ensures a seamless flow of critical data between devices and software.
Advantages include:
User Friendly
Tailored to meet the unique needs of your trial, providing data in formats compatible with your analysis tools.
Real-Time Data Integration
Automatically syncs medication adherence data with your trial software for immediate insights.
Simplified Implementation
Easy setup and support ensure minimal disruption to ongoing or planned trials.
Why Choose CuePath?
The Solutions We Offer
Building a reliable software application is not a one-off assignment. It requires grit and resilience.
Safety
Better adverse event monitoring, measure and manage diversion.
Retention
Significantly reduces need for in-clinic visits better for dignity and retention.
Acceptability
Rugged enough to handle any study population and easy to use
CuePath Innovation: Smart stickers for clinical trial blister packs
CuePath Innovation is a Vancouver-based provider of technology for monitoring and improving medication adherence. Our flagship product, the CuePack™, connects commonly available blister packs to the cloud and integrates seamlessly with Contract Research Organization (CRO) clinical trials management software.
CuePath addresses four key challenges in the clinical trial industry:
- Improve safety and dosage accuracy
- Reduce study burden without Daily Witnessed Ingestion
- Enhance reliability of efficacy analysis
- Prevent diversion of controlled substances
Our Impact
CuePath is proud to support the Canadian ASCME trial for methamphetamine use disorder treatment in partnership with ChangeMark Research + Evaluation. Our goal for 2025 is to expand partnerships within North America’s mental health and substance use clinical trials research communities.
How It Works
Revolutionizing Medication Adherence Monitoring
- CuePack™ Stickers
Our proprietary sticker technology attaches to standard blister packs and monitors medication intake in real time. - Cloud Connectivity
Data from the CuePack™ is transmitted to our secure cloud gateway and synced directly with CRO software. - Customization & Data Integration
CuePath offers fully customizable data exports to suit your study’s specific requirements. Whether integrating with systems like REDCap or adapting to unique workflows, we deliver meaningful, accurate data tailored to your needs. - Real-Time Insights
Researchers gain unparalleled visibility into participant medication compliance, allowing for swift interventions and accurate efficacy analysis.
What Clients Say
“We never really know if the patient has taken the drugs in our study. CuePath is the only company we know that gives us visibility into participants’ compliance in real-time.”
— Jill Fikowsky, CEO, ChangeMark Research + Evaluation
Our Projects
Current Trial
We are actively supporting the ASCME clinical trial for methamphetamine use disorder treatment. This pan-Canadian, multisite study, funded by Health Canada, is led by the University of Montreal Hospital Research Centre (CRCHUM).
Partnerships for the Future
Working closely with our BC-based CRO partner, ChangeMark, we aim to identify new opportunities in mental health and substance use clinical trials across North America in 2025.
Customization & Data Integration
Flexible Data Export & Workflow Integration
CuePath offers the capability to customize our system’s data exports and integrate seamlessly with a variety of clinical trial data platforms, including REDCap, and other third-party systems. Our services include:
- Tailored data formats to meet specific study requirements.
- Conversion and integration into different systems and workflows.
- Streamlining data management for improved efficiency and reliability.
Let us help you enhance your study’s data accuracy and compatibility while maintaining workflow flexibility.
Contact Us
Partner With CuePath
Interested in integrating CuePath’s innovative medication adherence solutions into your clinical trial? Let’s discuss how we can help enhance the safety, accuracy, and reliability of your studies.