Validation of the UK English Oxford Cognitive Screen-Plus in Sub-Acute and Chronic Stroke Survivors.
Abstract
Stroke survivors are routinely screened for cognitive impairment with tools that often fail to detect subtle impairments.
The Oxford Cognitive Screen-Plus (OCS-Plus) is a brief tablet-based screen designed to detect subtle post-stroke cognitive impairments.
We examined its psychometric properties in two stroke cohorts (subacute: <3 months post-stroke, chronic: >6 months post-stroke).
Patients and Methods This study included 347 stroke survivors (mean age = 73 years; mean education = 13 years; 43.06% female presenting; 74.42% ischaemic stroke).
The OCS-Plus was completed by 181 sub-acute stroke survivors and 166 chronic stroke survivors.
All participants also completed the Oxford Cognitive Screen (OCS) and a subset completed the Montreal Cognitive Assessment (MoCA) and further neuropsychological tests.
Results
First, convergent construct validity of all OCS-Plus tasks against task-matched standardized neuropsychological tests was confirmed.
Second, we evaluated divergent construct validity of all OCS-Plus subtasks.
Third, we report the sensitivity and specificity of each OCS-Plus subtask compared to neuropsychological test performance.
Fourth, we found that OCS-Plus detected cognitive impairments in a large proportion of those classed as unimpaired on MoCA and OCS.
Discussion and Conclusion The OCS-Plus provides a valid screening tool for sensitive detection of subtle cognitive impairment in stroke patients.
Indeed, the OCS-Plus detected subtle cognitive impairment at a similar level to validated neuropsychological assessments and exceeded detection of cognitive impairment compared to standard clinical screening tools.
Citations
Sam S Webb, Georgina Hobden, Rebecca Roberts, Evangeline G Chiu, Sarah King, and Nele Demeyere.Validation of the UK English Oxford Cognitive Screen-Plus in Sub-Acute and Chronic Stroke Survivors.PsyArXiv. June 9
Page last reviewed: 12 June, 2025
Metadata
Author(s): King, Sarah
Collection: 123456789/216
Format(s): Preprint
Date issued: 2022-06
ID: 1114