Clinical trials employ a variety of approaches to measure the health status of patients and changes in their health due to treatment. In many therapy areas, subjective ratings based on observations made by a clinician are used to measure status and changes over time.
There are a large number of validated subjective measurement scales are used in clinical trials to assess aspects of movement such as balance, specific movements, walking and mobility based on observation of the patient conducting a specified movement or activity.
Being subjective, these scales may not be very sensitive to detecting small improvements, and different investigators may rate patients differently based upon their interpretation of the scale requirements. For this reason it is sometimes difficult to find measurements that are sensitive enough to detect treatment-related changes and are able to conclusively show treatment effects when they exist. In addition, using investigator observation it is less likely that detailed or subtle aspects of movement and mobility can be recorded.
Within ICON’s Innovation lab, we have begun to develop prototype solutions that could be easily used in clinic to make objective assessments of aspects of movement and mobility. One approach leverages components of the Microsoft Xbox gaming platform. This motion-based gaming platform has brought with it the opportunity to use the same technology using in the gaming industry to assess motion and mobility in patients across a variety of conditions and application areas.
The Microsoft Kinect sensor, a component of the Xbox gaming system used to detect movement, has been particularly successful in enabling the development of health applications due to the ability of the Kinect to operate on a PC platform and the utility of its associated Software Development Kit (SDK) to facilitate the development of applications that track body movements.
A skeletal tracking module within the Kinect SDK enables the 3D position of 26 body joints to be tracked over time without the need for the patient to wear sensors, special clothing or special markers. Leveraging this has been the basis of our work to develop applications to assess movement.
In our proof of concept system, we convert the 3D coordinates of body joints provided by the Microsoft Kinect into vectors to enable us to calculate simple range of motion angles whilst the subject performs a number of shoulder movements:
A. Abduction
B. Adduction
C. Forward Flexion
D. Rotation
E. Internal and External rotation in abduction
While more testing is needed to assess the accuracy and utility of the application we have developed to measure shoulder range of motion, it is clear that the Microsoft Kinect platform offers a versatile and low-cost approach to measure novel health outcomes.
This may add significant value and utility to clinical drug development, in particular in replacing conventional subjective measures and enabling sophisticated measures of movement outside specialist laboratory settings.
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Digital Disruption
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Clinical trial data anonymisation and data sharing
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Clinical Trial Tokenisation
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Closing the evidence gap: The value of digital health technologies in supporting drug reimbursement decisions
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Digital disruption in biopharma
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Disruptive Innovation
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Personalising Digital Health
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The triad of trust: Navigating real-world healthcare data integration
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Patient Centricity
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Agile Clinical Monitoring
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Capturing the voice of the patient in clinical trials
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Charting the Managed Access Program Landscape
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Developing Nurse-Centric Medical Communications
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Exploring the patient perspective from different angles
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Patient safety and pharmacovigilance
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A guide to safety data migrations
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Taking safety reporting to the next level with automation
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Outsourced Pharmacovigilance Affiliate Solution
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The evolution of the Pharmacovigilance System Master File: Benefits, challenges, and opportunities
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Sponsor and CRO pharmacovigilance and safety alliances
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Understanding the Periodic Benefit-Risk Evaluation Report
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A guide to safety data migrations
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Patient Voice Survey - Decentralised and Hybrid Trials
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Reimagining Patient-Centricity with the Internet of Medical Things (IoMT)
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Using longitudinal qualitative research to capture the patient voice
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Agile Clinical Monitoring
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Regulatory Intelligence
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An innovative approach to rare disease clinical development
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Using innovative tools and lean writing processes to accelerate regulatory document writing
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Current overview of data sharing within clinical trial transparency
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Global Agency Meetings: A collaborative approach to drug development
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Keeping the end in mind: key considerations for creating plain language summaries
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Navigating orphan drug development from early phase to marketing authorisation
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Procedural and regulatory know-how for China biotechs in the EU
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RACE for Children Act
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Early engagement and regulatory considerations for biotech
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Requirements & strategy considerations within clinical trial transparency
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Spotlight on regulatory reforms in China
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Demystifying EU CTR, MDR and IVDR
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Transfer of marketing authorisation
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An innovative approach to rare disease clinical development
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Crossing the finish line: Why effective participation support strategy is critical to trial efficiency and success in rare diseases
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Diversity, equity and inclusion in rare disease clinical trials
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Identify and mitigate risks to rare disease clinical programmes
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Leveraging historical data for use in rare disease trials
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Natural history studies to improve drug development in rare diseases
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Patient Centricity in Orphan Drug Development
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The key to remarkable rare disease registries
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Therapeutic spotlight: Precision medicine considerations in rare diseases
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Advanced therapies for rare diseases
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Transforming Trials
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Ensuring the validity of clinical outcomes assessment (COA) data: The value of rater training
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Best practices to increase engagement with medical and scientific poster content
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Decentralised clinical trials
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Biopharma perspective: the promise of decentralised models and diversity in clinical trials
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Decentralised and Hybrid clinical trials
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Practical considerations in transitioning to hybrid or decentralised clinical trials
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Navigating the regulatory labyrinth of technology in decentralised clinical trials
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Biopharma perspective: the promise of decentralised models and diversity in clinical trials
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Implications of COVID-19 on statistical design and analyses of clinical studies
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Increasing Complexity and Declining ROI in Drug Development
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Payers Perspectives on Digital Therapeutics
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RWE Generation Cross Sectional Studies and Medical Chart Review
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Survey results: How to engage healthcare decision-makers
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