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Published in: The Patient - Patient-Centered Outcomes Research 5/2016

Open Access 01-10-2016 | Original Research Article

Cognitive Testing of an Electronic Version of the Faces Pain Scale-Revised with Pediatric and Adolescent Sickle Cell Patients

Authors: Neehar Gupta, April N. Naegeli, Diane M. Turner-Bowker, Emuella M. Flood, Lori Ellen Heath, Shelley M. Mays, Carlton Dampier

Published in: The Patient - Patient-Centered Outcomes Research | Issue 5/2016

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Abstract

Background

Patient diaries and pain scales can capture the course and complications of pain managed at home in children. The Faces Pain Scale-Revised (FPS-R) is a validated scale showing reliability in children, but it has not been validated in children with sickle cell disease (SCD).

Objective

The purpose of this study was to evaluate comprehension and usability of an electronic modified version of the FPS-R among pediatric patients with SCD.

Methods

This was a cross-sectional, qualitative study involving in-person interviews with children/adolescents from the USA and their parents/legal guardians. Interviews involved cognitive debriefing and usability testing of the FPS-R.

Results

In total, 22 children with SCD aged 4–17 years participated. Children aged 4–6 were generally unable to demonstrate clear understanding of the FPS-R and its response scale. Overall, children aged ≥7 years understood the instrument and could complete it on the electronic device, although children aged 7–8 often needed assistance from the parent. Children aged 9–17 years were able to read and complete the instrument independently. Most participants considered the electronic device easy to use.

Conclusions

The FPS-R was shown to be a comprehensible and usable pain measure for children aged 7–17 with SCD and to be beneficial for future clinical studies.
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Metadata
Title
Cognitive Testing of an Electronic Version of the Faces Pain Scale-Revised with Pediatric and Adolescent Sickle Cell Patients
Authors
Neehar Gupta
April N. Naegeli
Diane M. Turner-Bowker
Emuella M. Flood
Lori Ellen Heath
Shelley M. Mays
Carlton Dampier
Publication date
01-10-2016
Publisher
Springer International Publishing
Published in
The Patient - Patient-Centered Outcomes Research / Issue 5/2016
Print ISSN: 1178-1653
Electronic ISSN: 1178-1661
DOI
https://doi.org/10.1007/s40271-016-0166-z

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