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Early phase requirements assessment of a teletreatment trial
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Symposium on Applied Computing archive
Proceedings of the 2009 ACM symposium on Applied Computing table of contents
Honolulu, Hawaii
POSTER SESSION: Poster papers table of contents
Pages 395-396  
Year of Publication: 2009
ISBN:978-1-60558-166-8
Authors
I. Widya  University of Twente, The Netherlands
B. J. F. van Beijnum  University of Twente, The Netherlands
R. Bults  University of Twente, The Netherlands
V. Jones  University of Twente, The Netherlands
H. Hermens  University of Twente, The Netherlands
L. Sandsjö  University of Gothenburg, Sweden
L. Schaake  Roessingh Research and Development, The Netherlands
M. H. A. Huis in't Veld  Roessingh Research and Development, The Netherlands
Sponsor
SIGAPP: ACM Special Interest Group on Applied Computing
Publisher
ACM  New York, NY, USA
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ABSTRACT

This paper presents the early phase requirements elicitation of a teletreatment trial and the assessment of the requirements in respect of their importance to the trial and the feasibility of the corresponding adaptations of the telemedicine system within the trial project constraints. The elicitation approach and techniques adopt the particulars of the telemedicine working practices. The proposed approach not only uses the treatment description and scenario, it also utilizes the trial design. A trial design defines the settings of a trial and develops the treatment protocols such that treatment efficacy can be evaluated based on evidence. Such a design has to be a priori approved by a medical ethical committee, which may impose additional constraints that influence the elicited requirements. The approach therefore involves stakeholders who are not necessarily the users of the system to be. In line with the telemedicine working practices, the approach is moreover based on the identification and analysis of the tasks and task objectives associated to the responsibilities of the involved stakeholders. Furthermore, the elicitation is cyclic and applies a collection of known techniques and informal specification styles (e.g. tables and mock-ups). Results of the cycles converge to a set of requirements understood and agreed upon by the trial designers, who are medical professionals, typically unaware of the methods and techniques applied by engineers, but who co-shape the telemedicine system to be. This way of working manages expectations better, necessary in a telemedicine collaboration.


REFERENCES

Note: OCR errors may be found in this Reference List extracted from the full text article. ACM has opted to expose the complete List rather than only correct and linked references.

 
1
Chow, S-C., and Liu, J-P. 2004. Design and Analysis of Clinical Trials: Concepts and Methodologies, Wiley-Intersc.
 
2
Conway, B. J. NWP SAF: 1st User-Requirements Survey. EUMETSAT. http://www.metoffice.gov.uk, visited 8-1-'08.
 
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Collaborative Colleagues:
I. Widya: colleagues
B. J. F. van Beijnum: colleagues
R. Bults: colleagues
V. Jones: colleagues
H. Hermens: colleagues
L. Sandsjö: colleagues
L. Schaake: colleagues
M. H. A. Huis in't Veld: colleagues