Do we have to Include HCI Issues in Clinical Trials of Medical Devices?: – A Discussion
- ,
- ,
- Anne Sabers
- University of Copenhagen,
- Copenhagen University Hospital
Research Output:
Conference Article in Proceeding or Book/Report chapter
Article in proceedings
Peer-reviewOpen access
Publication Information
Output type
Research Output:
Conference Article in Proceeding or Book/Report chapter
Article in proceedings
Peer-reviewHost publication Subtitle
November 28-December 1, 2017, Brisbane, QLD, AustraliaOriginal language
EnglishPages from-to (Number of pages)
Pages 352-355 (4 pages)Publication milestones
- Published - 28/11/2017
Publication status
Published - 28/11/2017
Place of publication
BrisbanePublisher
Association for Computing Machinery, United StatesISBN (Electronic)
978-1-4503-5379-3 Publication IDs
- Scopus: 85044224245
Host publication title
OzCHI '17, Proceedings of the 29th Australian Conference on Computer-Human InteractionAbstract
Digital devices play an important role in medical treatment and will in the future play a larger role in connection to cures of health-related issues.
Traditionally medicine has been tested by clinical double blind, randomized trials to document the efficacy and safety profile. When it comes to the use of digital devices in treatments the protocols from the field of medicine is adopted. The question is whether or not this evidence based approach is useful when dealing with digital devices and whether the understanding of the efficiency of a treatment can be obtained without also looking at usability and lifestyle issues.
Based on a case study of epilepsy, a literature study of protocols for investigating treatments using digital medical devices, the set-up of studies, the design of a current protocol for clinical trials, and finally preliminary results, we discuss if clinical trials have to include usability studies to determine if a treatment is effective.
Traditionally medicine has been tested by clinical double blind, randomized trials to document the efficacy and safety profile. When it comes to the use of digital devices in treatments the protocols from the field of medicine is adopted. The question is whether or not this evidence based approach is useful when dealing with digital devices and whether the understanding of the efficiency of a treatment can be obtained without also looking at usability and lifestyle issues.
Based on a case study of epilepsy, a literature study of protocols for investigating treatments using digital medical devices, the set-up of studies, the design of a current protocol for clinical trials, and finally preliminary results, we discuss if clinical trials have to include usability studies to determine if a treatment is effective.
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Final published version, 284.03 KB
Related Event
Title
OZCHI17: Human-Nature
Event type
ConferenceDegree of recognition
International eventDate
28/11/2017 - 01/12/2017Location
Brisbane Brisbane, QLD, Australia
