Challenges for Data Collection in Clinical Trials for Low-Cost Wearable Health Monitors

Duration: 60 Minutes
Activity monitors, smart watches, patches are just some examples of wearable monitors. Health care is full of them, sleep monitors, EKGs, radiation exposure devices, and respirator devices to name a few. With more and more of these devices becoming common place, it's inevitable that researchers will want to mine this data. Collection and use of some of this data is already occurring as research participants are given the devices to wear and data collection goes into a research record. But, with the commonplace use of these devices for recreational purposes, it's safe to assume that a researcher at some point will ask to access and use data that was not originally generated for research purposes.
Data Collection in Clinical Trials
Instructor: Sarah Fowler Dixon
Product ID: 501882
Objectives of the Presentation
  • Types of devices being used and what is being collected
  • Federal regulations that come into play when wishing to access data
  • Privacy laws protecting data and data sharing
  • Examples of research done using this type of data
  • Technology considerations when collecting and sharing electronically captured data
  • Implications for data collections
Why Should you Attend
As this is an evolving area of research, many questions need to be addressed. Questions such as: What do the regulations have to say about these uses? Are there ethics that come into play? Are there privacy concerns and can the manufactures of these devices just share and use information for research purposes? Does this constitute big data and if so, are there implications? Attendance at this webinar will begin to provide answers and guidance for those wishing to pursue this venue of data collection.

Who will Benefit
This webinar will provide valuable assistance to all personnel in:
  • Human Subjects Research
  • Data management
  • Healthcare interested in exploring the field of Clinical Research
  • Clinical Research Coordinators
  • Principal Investigators/Physicians
  • Administration in charge of Clinical Research
  • Regulatory Compliance
$375
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  • Upon purchase of the recorded session a link will be updated on your OCP Account within 24 hours
  • Please click on the link to access the Recorded Session
  • Presentation handouts in downloadable PDF format will be updated on your OCP Account within 24 hours of the purchase of the product
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account after 48 hours of the product Purchase
  • Please share your valuable Feedback at the end of the session
Instructor Profile:
Sarah Fowler-Dixon, PhD, CIP is an Education Specialist and instructor with Washington University School of Medicine. She has developed a comprehensive education program for human subject research which has served as a model for other institutions. She crafted budgets, policies, procedures, reporting, and training for the new program. She has initiated the planning, development, authorship and implementation of many human subjects research policies, practices, guidelines, submission and reviewer forms often working with state and federal authorities.

She has provided consultation regarding ethical, federal, state, and institutional requirements for faculty and staff both in the design and execution of their projects and teaches research ethics and regulatory affairs and the fundamentals of research management to graduate and undergraduate students. More recently, she led a task force in the development of the Community Engaged Research Program at Washington University. Dr. Fowler-Dixon has simultaneously served as an Independent Consultant, providing expertise and creating supplemental educational materials, including a copyrighted workbook.

Prior to joining Washington University, Dr. Fowler-Dixon was the Educational Development and Learning Specialist for Saint Louis University serving on various committees to improve research, procedures, community outreach, and retention.
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