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General Medicine Neurology A

MoCA — Montreal Cognitive Assessment

30-point cognitive screening tool, more sensitive than the MMSE for mild cognitive impairment (Nasreddine 2005: cut-off 26 detected 90% of MCI and 100% of mild Alzheimer's disease).

Used in: Delirium & Cognitive Impairment Inflammatory Bowel Disease

How to use & interpret

The Montreal Cognitive Assessment (MoCA) is a 30-point screen that is more sensitive than the MMSE for mild cognitive impairment, testing executive function, attention, memory, language, visuospatial skills and orientation. A score of ≥26 is generally considered normal, and one point is added for people with 12 or fewer years of education.

It is a screening and monitoring tool, interpreted alongside history, functional impact and, where needed, further investigation — not a stand-alone diagnosis.

Score interpretation

Normal Cognition 26–30

MoCA ≥ 26 — normal cognitive performance

→ No specific cognitive intervention required; reassess if concerns arise clinically; repeat annually if risk factors for dementia present

Below the Normal Cut-Off (< 26) 0–25

MoCA < 26 — cognitive impairment possible. At this cut-off the MoCA detected 90% of mild cognitive impairment and 100% of mild Alzheimer's disease, with 87% specificity (Nasreddine 2005).

→ Full cognitive assessment and history from an informant; check reversible causes (thyroid, B12, folate, glucose, medication, mood); consider memory clinic referral; assess capacity, driving and safety; interpret in light of education, language and sensory impairment.

Interpretation bands for the MoCA. Apply clinical judgement and local guidance.

Frequently asked questions

MoCA or MMSE?

MoCA is more sensitive for mild cognitive impairment and executive dysfunction; MMSE is quicker and more familiar. MoCA is often preferred when early or subtle impairment is suspected.

References

Related

Curated clinical cross-links plus same-class fallbacks.

Decision support only — verify against a current formulary, NICE, or your local guideline before clinical use.