Proxy-reported sensory measures for children and adolescents with neurodevelopmental disorders: A systematic review

Nicolette Soler1,2, Reinie Cordier3,4, Iain E Perkes1,5,6

  • 1School of Health Sciences, University of Newcastle, Newcastle, NSW, Australia.

Insights

The Participation and Sensory Environment Questionnaire-Home (PSEQ-H) is the only sensory measure with moderate content validity and high-to-moderate psychometric properties for neurodevelopmental disorders. Consumer involvement is crucial for developing reliable sensory assessment tools.

Area of Science:

  • Neuroscience
  • Developmental Psychology
  • Psychometrics

Background:

  • Proxy-reported sensory measures are vital for assessing children with neurodevelopmental disorders (NDDs) like autism spectrum disorder and ADHD.
  • Evaluating the quality and utility of these measures is crucial for evidence-informed clinical practice.

Approach:

  • A systematic literature search identified 12 proxy-reported sensory measures for NDDs.
  • The Consensus-based Standards for the selection of health Measurement INstruments (COSMIN) Risk of Bias checklist and good measurement properties criteria were applied.
  • Findings were synthesized using a COSMIN adaptation of Grading of Recommendations, Assessment, Development and Evaluations.

Key Points:

  • Only three of the 12 measures provided sufficient data for evaluating content validity and psychometric properties.
  • The Participation and Sensory Environment Questionnaire-Home (PSEQ-H) was the sole measure meeting moderate content validity and moderate-to-high quality for psychometric properties.
  • PSEQ-H demonstrated structural validity, construct validity, internal consistency, reliability, and low measurement error.

Conclusions:

  • The PSEQ-H is a high-quality, psychometrically sound sensory measure for children with NDDs.
  • Consumer involvement in measure development significantly enhances content validity.
  • Ongoing evaluation of sensory measures against current standards is recommended to ensure clinical utility.
Abstract

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