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Screening tools for the identification of dementia for adults with age-related acquired hearing or vision impairment: a scoping review

  • Annie Pye (a1), Anna Pavlina Charalambous (a2), Iracema Leroi (a1) (a3), Chrysoulla Thodi (a2) and Piers Dawes (a4)...

Cognitive screening tests frequently rely on items being correctly heard or seen. We aimed to identify, describe, and evaluate the adaptation, validity, and availability of cognitive screening and assessment tools for dementia which have been developed or adapted for adults with acquired hearing and/or vision impairment.


Electronic databases were searched using subject terms “hearing disorders” OR “vision disorders” AND “cognitive assessment,” supplemented by exploring reference lists of included papers and via consultation with health professionals to identify additional literature.


1,551 papers were identified, of which 13 met inclusion criteria. Four papers related to tests adapted for hearing impairment; 11 papers related to tests adapted for vision impairment. Frequently adapted tests were the Mini-Mental State Examination (MMSE) and the Montreal Cognitive Assessment (MOCA). Adaptations for hearing impairment involved deleting or creating written versions for hearing-dependent items. Adaptations for vision impairment involved deleting vision-dependent items or spoken/tactile versions of visual tasks. No study reported validity of the test in relation to detection of dementia in people with hearing/vision impairment. Item deletion had a negative impact on the psychometric properties of the test.


While attempts have been made to adapt cognitive tests for people with acquired hearing and/or vision impairment, the primary limitation of these adaptations is that their validity in accurately detecting dementia among those with acquired hearing or vision impairment is yet to be established. It is likely that the sensitivity and specificity of the adapted versions are poorer than the original, especially if the adaptation involved item deletion. One solution would involve item substitution in an alternative sensory modality followed by re-validation of the adapted test.

Corresponding author
Correspondence should be addressed to: Dr. Piers Dawes, Manchester Centre for Audiology and Deafness, The University of Manchester and the Manchester Academic Health Sciences Centre, A3.09 Ellen Wilkinson Building, Manchester M13 9PL, UK. Phone: +44 161 306 1758; Fax: +44 161 275 3373. Email:
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Annie Pye and Anna Pavlina Charalambous are shared first author.

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