Aim: to compare the two new executive function tests of the revised Cambridge Cognitive Examination (CAMCOG-R), a bedside measure of cognitive function, with existing neuropsychological assessments of executive function in elderly stroke survivors. Methods: we assessed 83 stroke survivors at 1 and 3 months post-stroke with the new CAMCOG-R, the Weigl colour form sorting test and Raven's coloured progressive matrices. We assessed functional recovery with the Barthel index and depression with the self-report 15-item geriatric depression scale. We used descriptive statistics, Pearson correlation coefficients, paired t-tests and principal axis factor analyses to interpret the data. Results: the new CAMCOG-R executive functioning tests showed moderate correlation with the Weigl and Raven tests (P < 0.01). Improved functional outcome as measured by the Barthel index was significantly associated with higher executive function test scores (P < 0.05). Depression was significantly associated with poorer performance on all tasks of executive function (P < 0.05). A factor analysis of the scores on all of the neuropsychological tests revealed a single strong factor that accounted for 66% of the variance. The CAMCOG-R and the executive functioning subscales used in this population established sensitivity to change over time. Conclusion: although the new executive tests of the CAMCOG-R compared reasonably well with the Weigl and Raven neuropsychological tests, the extra time taken to administer the CAMCOG-R may not be justified. The new CAMCOG-R executive function tests were vulnerable to the effects of depression. Finally, the executive function tests might have provided more of a global measure of cognitive function, raising doubts about their construct validity in our patient population.
CITATION STYLE
Leeds, L., Meara, R. J., Woods, R., & Hobson, J. P. (2001). A comparison of the new executive functioning domains of the CAMCOG-R with existing tests of executive function in elderly stroke survivors. Age and Ageing, 30(3), 251–254. https://doi.org/10.1093/ageing/30.3.251
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