Skip to main content
Journal of Neurology, Neurosurgery, and Psychiatry logoLink to Journal of Neurology, Neurosurgery, and Psychiatry
. 1998 May;64(5):588–594. doi: 10.1136/jnnp.64.5.588

CLOX: an executive clock drawing task

D Royall 1, J Cordes 1, M Polk 1
PMCID: PMC2170069  PMID: 9598672

Abstract

OBJECTIVE—To describe a clock drawing task (CLOX) designed to elicit executive impairment and discriminate it from non-executive constructional failure.
SUBJECTS—90 elderly subjects were studied (45 elderly and well persons from the independent living apartments of a continuing care retirement community and 45 patients with probable Alzheimer's disease). The clock drawing performance of elderly patients was compared with that of 62 young adult controls.
METHODS—Subjects received the CLOX, an executive test (EXIT25), and the mini mental state examination (MMSE). The CLOX is divided into an unprompted task that is sensitive to executive control (CLOX1) and a copied version that is not (CLOX2). Between rater reliability (27 subjects) was high for both subtests.
RESULTS—In elderly subjects, CLOX subscores correlated strongly with cognitive severity (CLOX1: r=−0.83 v the EXIT25; CLOX2: r=0.85 v the MMSE). EXIT25 and MMSE scores predicted CLOX1 scores independently of age or education (F(4,82)=50.7, p<0.001; R2=0.71). The EXIT25 accounted for 68% of CLOX1 variance. Only the MMSE significantly contributed to CLOX2 scores (F(4,72)= 57.2,p<0.001; R2=0.74). CLOX subscales discriminated between patients with Alzheimer's disease and elderly controls (83.1% of cases correctly classified; Wilkes' lambda=0.48, p<0.001), and between Alzheimer's disease subgroups with and without constructional impairment (91.9% of cases correctly classified; Wilkes' lambda=0.31, p<0.001).
CONCLUSIONS—The CLOX is an internally consistent measure that is easy to administer and displays good inter-rater reliability. It is strongly associated with cognitive test scores. The pattern of CLOX failures may discriminate clinical dementia subgroups.



Full Text

The Full Text of this article is available as a PDF (184.1 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Ainslie N. K., Murden R. A. Effect of education on the clock-drawing dementia screen in non-demented elderly persons. J Am Geriatr Soc. 1993 Mar;41(3):249–252. doi: 10.1111/j.1532-5415.1993.tb06701.x. [DOI] [PubMed] [Google Scholar]
  2. Axelrod B. N., Goldman R. S., Henry R. R. Sensitivity of the Mini-Mental State Examination to frontal lobe dysfunction in normal aging. J Clin Psychol. 1992 Jan;48(1):68–71. doi: 10.1002/1097-4679(199201)48:1<68::aid-jclp2270480110>3.0.co;2-n. [DOI] [PubMed] [Google Scholar]
  3. Celsis P., Agniel A., Puel M., Le Tinnier A., Viallard G., Démonet J. F., Rascol A., Marc-Vergnes J. P. Lateral asymmetries in primary degenerative dementia of the Alzheimer type. A correlative study of cognitive, haemodynamic and EEG data, in relation with severity, age of onset and sex. Cortex. 1990 Dec;26(4):585–596. doi: 10.1016/s0010-9452(13)80308-5. [DOI] [PubMed] [Google Scholar]
  4. Coffey C. E., Wilkinson W. E., Parashos I. A., Soady S. A., Sullivan R. J., Patterson L. J., Figiel G. S., Webb M. C., Spritzer C. E., Djang W. T. Quantitative cerebral anatomy of the aging human brain: a cross-sectional study using magnetic resonance imaging. Neurology. 1992 Mar;42(3 Pt 1):527–536. doi: 10.1212/wnl.42.3.527. [DOI] [PubMed] [Google Scholar]
  5. Folstein M. F., Folstein S. E., McHugh P. R. "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res. 1975 Nov;12(3):189–198. doi: 10.1016/0022-3956(75)90026-6. [DOI] [PubMed] [Google Scholar]
  6. Grady C. L., Haxby J. V., Schapiro M. B., Gonzalez-Aviles A., Kumar A., Ball M. J., Heston L., Rapoport S. I. Subgroups in dementia of the Alzheimer type identified using positron emission tomography. J Neuropsychiatry Clin Neurosci. 1990 Fall;2(4):373–384. doi: 10.1176/jnp.2.4.373. [DOI] [PubMed] [Google Scholar]
  7. Haxby J. V., Grady C. L., Koss E., Horwitz B., Heston L., Schapiro M., Friedland R. P., Rapoport S. I. Longitudinal study of cerebral metabolic asymmetries and associated neuropsychological patterns in early dementia of the Alzheimer type. Arch Neurol. 1990 Jul;47(7):753–760. doi: 10.1001/archneur.1990.00530070043010. [DOI] [PubMed] [Google Scholar]
  8. Huntzinger J. A., Rosse R. B., Schwartz B. L., Ross L. A., Deutsch S. I. Clock drawing in the screening assessment of cognitive impairment in an ambulatory care setting: a preliminary report. Gen Hosp Psychiatry. 1992 Mar;14(2):142–144. doi: 10.1016/0163-8343(92)90040-h. [DOI] [PubMed] [Google Scholar]
  9. Kirk A., Kertesz A. On drawing impairment in Alzheimer's disease. Arch Neurol. 1991 Jan;48(1):73–77. doi: 10.1001/archneur.1991.00530130083024. [DOI] [PubMed] [Google Scholar]
  10. Kuhl D. E., Metter E. J., Riege W. H., Hawkins R. A. The effect of normal aging on patterns of local cerebral glucose utilization. Ann Neurol. 1984;15 (Suppl):S133–S137. doi: 10.1002/ana.410150726. [DOI] [PubMed] [Google Scholar]
  11. Lee H., Lawlor B. A. State-dependent nature of the clock drawing task in geriatric depression. J Am Geriatr Soc. 1995 Jul;43(7):796–798. doi: 10.1111/j.1532-5415.1995.tb07054.x. [DOI] [PubMed] [Google Scholar]
  12. Manos P. J., Wu R. The ten point clock test: a quick screen and grading method for cognitive impairment in medical and surgical patients. Int J Psychiatry Med. 1994;24(3):229–244. doi: 10.2190/5A0F-936P-VG8N-0F5R. [DOI] [PubMed] [Google Scholar]
  13. McKhann G., Drachman D., Folstein M., Katzman R., Price D., Stadlan E. M. Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease. Neurology. 1984 Jul;34(7):939–944. doi: 10.1212/wnl.34.7.939. [DOI] [PubMed] [Google Scholar]
  14. Mendez M. F., Ala T., Underwood K. L. Development of scoring criteria for the clock drawing task in Alzheimer's disease. J Am Geriatr Soc. 1992 Nov;40(11):1095–1099. doi: 10.1111/j.1532-5415.1992.tb01796.x. [DOI] [PubMed] [Google Scholar]
  15. Motomura N., Seo T. Lateral hemispheric asymmetries in senile dementia of Alzheimer's type (SDAT) assessed by I-123 IMP SPECT imaging: a preliminary report. Int J Neurosci. 1992 Mar;63(1-2):1–3. doi: 10.3109/00207459208986655. [DOI] [PubMed] [Google Scholar]
  16. Nelson A., Fogel B. S., Faust D. Bedside cognitive screening instruments. A critical assessment. J Nerv Ment Dis. 1986 Feb;174(2):73–83. doi: 10.1097/00005053-198602000-00002. [DOI] [PubMed] [Google Scholar]
  17. Ober B. A., Jagust W. J., Koss E., Delis D. C., Friedland R. P. Visuoconstructive performance and regional cerebral glucose metabolism in Alzheimer's disease. J Clin Exp Neuropsychol. 1991 Sep;13(5):752–772. doi: 10.1080/01688639108401088. [DOI] [PubMed] [Google Scholar]
  18. PIERCY M., SMYTH V. O. Right hemisphere dominance for certain non verbal intellectual skills. Brain. 1962 Dec;85:775–790. doi: 10.1093/brain/85.4.775. [DOI] [PubMed] [Google Scholar]
  19. Rouleau I., Salmon D. P., Butters N., Kennedy C., McGuire K. Quantitative and qualitative analyses of clock drawings in Alzheimer's and Huntington's disease. Brain Cogn. 1992 Jan;18(1):70–87. doi: 10.1016/0278-2626(92)90112-y. [DOI] [PubMed] [Google Scholar]
  20. Royall D. R. Comments on the executive control of clock-drawing. J Am Geriatr Soc. 1996 Feb;44(2):218–219. doi: 10.1111/j.1532-5415.1996.tb02452.x. [DOI] [PubMed] [Google Scholar]
  21. Royall D. R., Mahurin R. K., Gray K. F. Bedside assessment of executive cognitive impairment: the executive interview. J Am Geriatr Soc. 1992 Dec;40(12):1221–1226. doi: 10.1111/j.1532-5415.1992.tb03646.x. [DOI] [PubMed] [Google Scholar]
  22. Royall D. R., Mahurin R. Qualitative assessment of dementia. J Am Geriatr Soc. 1994 Jul;42(7):798–799. doi: 10.1111/j.1532-5415.1994.tb06548.x. [DOI] [PubMed] [Google Scholar]
  23. Royall D. R., Polk M. Dementias that present with and without posterior cortical features: an important clinical distinction. J Am Geriatr Soc. 1998 Jan;46(1):98–105. doi: 10.1111/j.1532-5415.1998.tb01022.x. [DOI] [PubMed] [Google Scholar]
  24. Royall D. R. Precis of executive dyscontrol as a cause of problem behavior in dementia. Exp Aging Res. 1994 Apr-Jun;20(2):73–94. doi: 10.1080/03610739408253955. [DOI] [PubMed] [Google Scholar]
  25. Sawada H., Udaka F., Kameyama M., Seriu N., Nishinaka K., Shindou K., Kodama M., Nishitani N., Okumiya K. SPECT findings in Parkinson's disease associated with dementia. J Neurol Neurosurg Psychiatry. 1992 Oct;55(10):960–963. doi: 10.1136/jnnp.55.10.960. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Tuokko H., Hadjistavropoulos T., Miller J. A., Beattie B. L. The Clock Test: a sensitive measure to differentiate normal elderly from those with Alzheimer disease. J Am Geriatr Soc. 1992 Jun;40(6):579–584. doi: 10.1111/j.1532-5415.1992.tb02106.x. [DOI] [PubMed] [Google Scholar]
  27. Watson Y. I., Arfken C. L., Birge S. J. Clock completion: an objective screening test for dementia. J Am Geriatr Soc. 1993 Nov;41(11):1235–1240. doi: 10.1111/j.1532-5415.1993.tb07308.x. [DOI] [PubMed] [Google Scholar]
  28. Wolf-Klein G. P., Silverstone F. A., Levy A. P., Brod M. S. Screening for Alzheimer's disease by clock drawing. J Am Geriatr Soc. 1989 Aug;37(8):730–734. doi: 10.1111/j.1532-5415.1989.tb02234.x. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Neurology, Neurosurgery, and Psychiatry are provided here courtesy of BMJ Publishing Group

RESOURCES