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

Neehar Gupta1, April N Naegeli2, Diane M Turner-Bowker3

  • 1Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, 46285, USA. ngupta@lilly.com.

The Patient
|March 31, 2016
PubMed

Insights

The electronic Faces Pain Scale-Revised (FPS-R) is understandable for children aged 7 and older with sickle cell disease (SCD). This validated pain scale is useful for future clinical studies involving pediatric SCD patients.

Area of Science:

  • Pediatric Hematology
  • Pain Management
  • Clinical Informatics

Background:

  • Patient-reported outcomes are crucial for managing pediatric pain at home.
  • The Faces Pain Scale-Revised (FPS-R) is a reliable pain assessment tool for children.
  • Validation of the FPS-R in children with sickle cell disease (SCD) is lacking.

Purpose of the Study:

  • To assess the comprehension and usability of an electronic, modified FPS-R in pediatric patients with SCD.
  • To determine the age-appropriateness and ease of use of the electronic FPS-R for SCD patients.

Main Methods:

  • A cross-sectional, qualitative study design was employed.
  • In-person interviews and cognitive debriefing were conducted with children (4-17 years) with SCD and their parents in the USA.
  • Usability testing of the electronic FPS-R was performed.

Main Results:

  • Children aged 4-6 years demonstrated limited understanding of the FPS-R.
  • Children aged 7-8 years understood the scale but often required parental assistance.
  • Children aged 9-17 years could independently comprehend and use the electronic FPS-R.
  • The majority of participants found the electronic device user-friendly.

Conclusions:

  • The electronic FPS-R is a comprehensible and usable pain measurement tool for children aged 7-17 with SCD.
  • The validated electronic FPS-R can be beneficial for future clinical research in pediatric SCD.
  • This study supports the use of digital pain assessment tools in managing SCD pain.
Abstract

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