Evidence map›Paper›PMID 40376142›Full record

ArticleAlzheimer's & dementia (New York, N. Y.)

Three approaches to determining clinically meaningful benefit on the Cohen-Mansfield Agitation Inventory in dementia clinical trials for agitation.

Kathy Y Liu, Chineze Ivenso, Rebecca Howard, Penny Rapaport, Suzanne Reeves, Sube Banerjee, Lon S Schneider, Maria I Lapid, Agitation MCID Study Group, Robert Howard

Abstract read
In one paragraph

Article in Alzheimer's & dementia (New York, N. Y.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Toward Precision Neuropsychiatry of Dementia: Neuropsychiatric Symptoms as Multidimensional Clinical Phenotypes.Psychogeriatrics : the official journal of the Japanese Psychogeriatric Society · 2026
    Review
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Kathy Y LiuDivision of Psychiatry University College London London UK.
Chineze IvensoAneurin Bevan University Health Board St Cadoc's Hospital Newport Wales UK.
Rebecca HowardSouth London and Maudsley NHS Foundation Trust Maudsley Hospital London UK.
Penny RapaportDivision of Psychiatry University College London London UK.
Suzanne ReevesDivision of Psychiatry University College London London UK.
Sube BanerjeeFaculty of Medicine and Health Sciences University of Nottingham Medical School, Queen's Medical Centre Nottingham UK.
Lon S SchneiderDepartment of Psychiatry and the Behavioral Sciences, and Department of Neurology Keck School of Medicine, and Leonard Davis School of Gerontology of the University of Southern California Los Angeles California USA.
Maria I LapidDepartment of Psychiatry & Psychology Mayo Clinic Rochester Minnesota USA.
Agitation MCID Study Group
Robert HowardDivision of Psychiatry University College London London UK.

Funding

USCADRC Diversity Supplement PachicanoP30AG066530 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI HELENA Chang CHUI · 2020 to 2026
$27.8M
A Randomized Controlled Trial of Electroconvulsive Therapy plus Usual Care versus Simulated-ECT plus Usual Care for the Acute Management of Severe Agitation in Alzheimer's Dementia (ECT-AD)R01AG061100 · NIA · MCLEAN HOSPITAL · PI FORESTER, BRENT PETER, PETRIDES, GEORGIOS · 2018 to 2023
$9.4M
NIA NIH HHS P30 AG066530NIA NIH HHS R01 AG061100
6 · The paper itself

Abstract

introductionThere is a need to understand the clinical meaningfulness of symptom score changes in treatment trials of dementia-related agitation. We estimated minimal clinically important differences (MCIDs) for commonly employed agitation scales and contextualized their clinical application.

methodsWe employed anchor- and distribution-based approaches to determine changes in scores corresponding to minimal symptom improvement. An opinion-based approach assessed expert clinicians' agreement on the meaningfulness of score changes through three clinical vignettes.

resultsMinimal symptom improvement for Cohen-Mansfield Agitation Inventory total score ranged from -4 (over <1 month) to -11 (over 1 to 3 months) points. Greater symptom severity correlated with higher MCID estimates. The clinical importance of score changes was influenced by treatment duration, pharmacological side effects, and impacts on caregiver distress/time resources. DISCUSSION: The clinical meaningfulness of agitation scale MCIDs is influenced by trial-specific and clinical factors. Shorter trial durations and measuring caregiver distress/time resources enhance the clinical interpretation of agitation treatment outcomes. Highlights: For the CMAI total score, the MCID was -4 points over shorter time scales and -11 points for longer time scales.Worse agitation severity was associated with higher MCID estimates.There was high expert consensus that a noticeable treatment benefit was not worthwhile if it occurred after 12 weeks or had no impact on caregiver/staff distress/time resources.

Indexed as

agitationAlzheimerclinically meaningful benefitdementiaMCIDtrial

Identifiers

PMID40376142
PMCPMC12079343

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.