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Spanish adaptation of the Rasch-Built Overall Amyotrophic Lateral Sclerosis Disability Scale (ROADS).

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Summary

The Spanish Rasch-Built Overall Amyotrophic Lateral Sclerosis Disability Scale (ROADS) is a reliable and valid tool for measuring functional decline in people with ALS. This validated Spanish ROADS measure offers a comprehensive assessment for Spanish-speaking individuals with ALS.

Keywords:
Amyotrophic lateral sclerosisSpanishfunctional rating scalevalidation

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Area of Science:

  • Neurology
  • Rehabilitation Medicine
  • Biomedical Statistics

Background:

  • Amyotrophic lateral sclerosis (ALS) causes progressive functional decline.
  • The ALS Functional Rating Scale-Revised (ALSFRS-R) is the traditional measure of disability.
  • The Rasch-Built Overall Amyotrophic Lateral Sclerosis Disability Scale (ROADS) offers a more comprehensive assessment but lacked a Spanish translation.

Purpose of the Study:

  • To translate the ROADS scale into Spanish.
  • To validate the psychometric properties of the Spanish ROADS scale.
  • To establish a reliable and valid functional disability measure for Spanish-speaking people with ALS (pwALS).

Main Methods:

  • Translation and cultural adaptation of the ROADS scale.
  • Recruitment of 53 Spanish-speaking pwALS.
  • Administration of the Spanish ROADS and ALSFRS-R.
  • Statistical analysis of reliability (internal consistency, test-retest) and validity (correlation with ALSFRS-R).

Main Results:

  • Excellent internal consistency reliability for the Spanish ROADS (Cronbach's alpha = 0.94).
  • High test-retest reliability (intra-class correlation = 0.93).
  • Strong significant correlation between Spanish ROADS and ALSFRS-R total scores (rs = .89, p < .001).
  • Significant correlations between specific subscales and items, supporting domain-to-item validity.

Conclusions:

  • The Spanish ROADS is a psychometrically robust measure.
  • It is a valid and reliable tool for quantifying functional disability in Spanish-speaking pwALS.
  • This validated scale enhances the assessment of ALS progression in a diverse population.