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The IQCODE is an informant-based questionnaire that can supplement or replace cognitive testing. Cognitive Screening Instruments: A Practical Approach, pp. The general practitioner assessment of cognition (GPCOG). What Is the Best Dementia Screening Instrument for General Practitioners to Use? American Journal of Geriatric Psychiatry, 14(5), 391–400.

Brodaty, H., Lee-Fay, L., Gibson, L., & Burns, K.International Journal of Geriatric Psychiatry, 19(9), 870–874. Characteristics of the GPCOG, a screening tool for cognitive impairment. Journal of the American Geriatrics Society, 50(3), 530–534. The GPCOG: a new screening test for dementia designed for general practice. M., Luscombe, G., Harding, L., Berman, K., & Huppert, F. For more information and to obtain permission for commercial use, visit the GPCOG website. The GPCOG can be used freely for non-commercial purposes. The GPCOG is administered by healthcare professionals. It has been translated to several languages and has been consistently shown to match or outperform longer scales in detecting dementia. It consists of a short patient examination (<4 min) and an optional informant interview (2 min). The GPCOG was developed to assist General Practitioners and other primary healthcare workers to detect cognitive impairment and dementia. Psychiatry and Clinical Neurosciences, 61(1), 78–83. Reliability and validity of the Japanese version of the Frontal Assessment Battery in patients with the frontal variant of frontotemporal dementia. The FAB: A frontal assessment battery at bedside. Dubois, B., Slachevsky, A., Litvan, I., & Pillon, B.The FAB is administered by healthcare professionals in a structured interview format. There is evidence the FAB can accurately distinguish persons with frontal lobe dysfunction due to frontotemporal dementia from those with Alzheimer’s disease. It can be administered in many settings and is well-accepted by consumers. The FAB is a brief screen for executive dysfunction associated with damage to the frontal lobe. The AD8: a brief informant interview to detect dementia. For more information on permission and licensing, please visit the AD8 website or the licensing page of the University of Washington in St. The AD8 can be used without modification or editing of any kind solely for clinical care purposes and non-commercial research.

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The AD8 is administered by a healthcare professional or research assistant.

It has mostly been validated in high-prevalence settings such as emergency departments and dementia clinics, and has been adapted for many different languages. The AD8 is a very brief eight-item informant interview designed to differentiate between normal ageing and dementia. A new rating scale for Alzheimer’s disease. Alzheimer Dis Assoc Disord, 11 Suppl 2: S13–21. The Alzheimer’s Disease Cooperative Study. Development of cognitive instruments for use in clinical trials of antidementia drugs: additions to the Alzheimer’s Disease Assessment Scale that broaden its scope. H., Ernesto, C., Grundman, M., Sano, M., Bieliauskas, L., Geldmacher, D., Clark, C., & Thal, L. For other uses, please contact the original authors to seek permission. Training is required and can be obtained from the authors or from the Alzheimer’s Disease Cooperative Study.įree of charge to healthcare professionals for non-commercial clinical or research purposes. The ADAS-COG is administered by a neuropsychologist or psychologist.

ADAS-COG is widely used as an outcome measure in drug and therapy treatments aimed at delaying cognitive decline in dementia. It is recommended for second-stage or in-depth assessments and/or for particular research evaluations rather than for applications in routine care settings. The ADAS-COG is used for comprehensive cognitive assessment. Cognitive Tests to Detect Dementia: A Systematic Review and Meta-analysis. Dementia and Geriatric Cognitive Disorders, 36(3–4), 242. Validation of the Addenbrooke’s Cognitive Examination III in frontotemporal dementia and Alzheimer’s disease.

Hsieh, S., Schubert, S., Hoon, C., Mioshi, E., & Hodges, J.

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The ACE-III can be used for free in clinical practice and research projects. The ACE-III is administered by healthcare professionals. It is useful for differential diagnosis between Alzheimer’s disease (AD), frontotemporal dementia (FTD), Parkinson’s disease dementia and related neurodegenerative conditions. The ACE-III is a comprehensive screening tool that is the recommended instrument for all dementias when shorter screens are inconclusive.

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