User Experience Registry for Generalizable Usability Assessment

Usability assessment is a crucial component in human-centered design (HCD) throughout the systems development lifecycle (SDLC). Sound usability assessment ensures users to operate the system effectively, efficiently, and with satisfaction. However, in the reality of frequent releases and tight development schedules, formative testing is often reduced and summative testing eliminated. To address these challenges, this position paper proposes a framework for a user experience registry as a solution to aggregating data collected from formative testing, with the goal of improving the robustness and generalizability of the findings based on such data.

Content

Author and article information

Contributors

Lin Wang

Conference

Publication date: July 2018

Publication date (Print): July 2018

Pages: 1-4

Affiliations

[0001]U.S. Census Bureau

Washington D.C., USA

Article

DOI: 10.14236/ewic/HCI2018.66

SO-VID: b9b4838a-fa0a-41a4-98e8-74c7524ff7b4

License:

This work is licensed under a Creative Commons Attribution 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

Conference name: Proceedings of the 32nd International BCS Human Computer Interaction Conference

Conference acronym: HCI

Conference number: 32

Conference location: Belfast, UK

Conference date: 4 - 6 July 2018

Conference sponsor: Electronic Workshops in Computing (eWiC)

Conference theme: Human Computer Interaction Conference

History

Product

1477-9358 BCS Learning & Development

Self URI (article page): https://www.scienceopen.com/hosted-document?doi=10.14236/ewic/HCI2018.66

Self URI (journal page): https://ewic.bcs.org/

References

RE GliklichNA Dreyer 2010 Registries for Evaluating Patient Outcomes: A User’s Guide 2nd Agency for Healthcare Research and Quality Rockville, MD
National Quality Registry Network 2014 What is a Clinical Data Registry? American Medical Association
Workman TA 2013 Engaging Patients in Information Sharing and Data Collection: The Role of Patient-Powered Registries and Research Networks AHRQ Community Forum White Paper AHRQ Publication No. 13-EHC124-EF Rockville, MD Agency for Healthcare Research and Quality
ISO 9241-11 2015 Ergonomics of human-system interaction — Part 11: Usability: Def-initions and concepts International Organization for Standardization Geneva
RM GrovesFJ FowlerMP Couper, JM LepkowsckiE SingerR. Tourangeau 2009 Survey Methodology Wiley, New Jersey

Comments

Comment on this article

[1] RE GliklichNA Dreyer 2010 Registries for Evaluating Patient Outcomes: A User’s Guide 2nd Agency for Healthcare Research and Quality Rockville, MD

[2] National Quality Registry Network 2014 What is a Clinical Data Registry? American Medical Association

[3] Workman TA 2013 Engaging Patients in Information Sharing and Data Collection: The Role of Patient-Powered Registries and Research Networks AHRQ Community Forum White Paper AHRQ Publication No. 13-EHC124-EF Rockville, MD Agency for Healthcare Research and Quality

[4] ISO 9241-11 2015 Ergonomics of human-system interaction — Part 11: Usability: Def-initions and concepts International Organization for Standardization Geneva

[5] RM GrovesFJ FowlerMP Couper, JM LepkowsckiE SingerR. Tourangeau 2009 Survey Methodology Wiley, New Jersey

Celebrating 65 years of The Computer Journal - free-to-read perspectives - bcs.org/tcj65