Psychometric properties of the Belgian LDCDQ (LDCDQ-BE) in a population based sample

Amy De Roubaix1, Hilde Van Waelvelde1

  • 1Faculty of Medicine and Health Care Sciences, Department of Rehabilitation Sciences, Ghent University, Entrance 46, UZ Ghent, C. Heymanslaan 10, 9000 Ghent, Belgium.

Insights

The Little Developmental Coordination Questionnaire-Belgian version (LDCDQ-BE) shows good internal consistency for identifying young children at risk of Developmental Coordination Disorder (DCD). However, its predictive validity requires further investigation before clinical use.

Area of Science:

  • Pediatrics
  • Neurodevelopmental Disorders
  • Psychometrics

Background:

  • Developmental Coordination Disorder (DCD) is a neurodevelopmental condition typically diagnosed in school-aged children.
  • Early identification of DCD is crucial due to potential secondary consequences.
  • The Little Developmental Coordination Questionnaire (LDCDQ) is a screening tool for children at risk of DCD.

Purpose of the Study:

  • To evaluate the psychometric properties of the Belgian version of the LDCDQ (LDCDQ-BE).
  • To determine appropriate cut-off scores for the LDCDQ-BE in a Belgian population.

Main Methods:

  • Parental (n=637) and teacher (n=249) questionnaires were administered to children aged 3-5 years.
  • Motor development was assessed using the M-ABC-2, Beery-VMI-6, and teacher's Motor Skill Checklist (MSC) in a subset of 82 children.

Main Results:

  • The LDCDQ-BE exhibited excellent internal consistency (Cronbach's α=0.92).
  • Convergent validity was moderate with M-ABC-2 (r=0.42), and weak to moderate with Beery-VMI-6 (r=0.30-0.31) and MSC (r=0.27).
  • Discriminant validity was poor for M-ABC-2 and Beery-VMI-6 Visual-Motor Integration, but moderate for Beery-VMI-6 Motor Coordination and MSC.

Conclusions:

  • The LDCDQ-BE demonstrates acceptable psychometric properties for screening purposes.
  • Sensitivity of the LDCDQ-BE is low to moderate.
  • Further research is needed to establish the predictive validity of the LDCDQ-BE for diagnosing DCD.
Abstract

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