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Developing Standards to Support the Use of Wearables and Sensors for Objective Data Collection During Clinical Trials
Session Chair(s)
Jennifer Goldsack, MA, MBA, MS
Chief Executive Officer
Digital Medicine Society (DiMe), United States
Seating is limited.
The DIA Study Endpoints Community has convened a working group to drive the science around the use of wearable technology and the development of study endpoints from wearables data. Broad adoption of wearables and sensors for objective data capture in pivotal studies is being impeded by the absence of standards. In this discussion, participants will evaluate and provide feedback on proposed solutions intended to address this challenge.
Learning Objective : Review and discuss the current work of Study Endpoint Community’s Wearables Work Group, and the Standards Work Stream; Evaluate the the adoption of wearables and sensors for objective data capture in clinical trials.
Speaker(s)
Facilitator
Susan Vallow, MBA, RPH
Worldwide Clinical Trials, United States
Executive Director, Patient-Centered Outcomes Research
Facilitator
Marie McCarthy, MSC
Novartis, Ireland
Digital Endpoint Lead
Facilitator
Paul O'Donohoe, MS, MSC
Medidata Solutions, United States
Senior Director, eCOA Product and Science