Evidence map›Paper›PMID 40792595›Full record

ArticleJournal of the American Heart Association2025

Cognitive Assessments in Randomized Controlled Trials of Acute or Secondary Prevention Stroke Treatments 2011 to 2024: A Scoping Review.

Sajeevan Sujanthan, Jesse Buchman, Aaron Herlick, Damyen Henderson-Lee Wah, William Betzner, Alisia Southwell, Theresa Aves, Pugaliya Puveendrakumaran, Idris Fatakdawala, Vanessa Norouzi and 11 more

Abstract readScoping Review
In one paragraph

Article in Journal of the American Heart Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. Review
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

21 authors.

Sajeevan SujanthanInstitute of Medical Science, University of Toronto Ontario Canada.ORCID 0000-0002-3128-3977
Jesse BuchmanDepartment of Medicine (Neurology), Sunnybrook Health Sciences Centre Toronto Ontario Canada.
Aaron HerlickDepartment of Medicine (Neurology), Sunnybrook Health Sciences Centre Toronto Ontario Canada.ORCID 0000-0003-3474-0608
Damyen Henderson-Lee WahInstitute of Health Policy, Management and Evaluation University of Toronto Ontario Canada.ORCID 0009-0004-6237-6174
William BetznerUniversity of Calgary Alberta Canada.ORCID 0000-0002-9071-0705
Alisia SouthwellDepartment of Medicine (Neurology), Sunnybrook Health Sciences Centre Toronto Ontario Canada.
Theresa AvesInstitute of Health Policy, Management and Evaluation University of Toronto Ontario Canada.
Pugaliya PuveendrakumaranDepartment of Medicine (Neurology), Sunnybrook Health Sciences Centre Toronto Ontario Canada.
Idris FatakdawalaDepartment of Medicine (Neurology), Sunnybrook Health Sciences Centre Toronto Ontario Canada.
Vanessa NorouziDepartment of Medicine (Neurology), Sunnybrook Health Sciences Centre Toronto Ontario Canada.
Teruko KishibeLibrary Service, Unity Health Toronto Toronto Ontario Canada.ORCID 0000-0001-8797-7137
Michael D HillDepartment of Clinical Neurosciences and Hotchkiss Brain Institute, Cumming School of Medicine University of Calgary Alberta Canada.ORCID 0000-0002-6269-1543
Raed A JoundiDepartment of Medicine, Division of Neurology McMaster University Hamilton Ontario Canada.ORCID 0000-0001-9554-0701
Ryan T MuirDepartment of Medicine (Neurology), Sunnybrook Health Sciences Centre Toronto Ontario Canada.ORCID 0000-0002-9349-1069
Bijoy K MenonDepartment of Clinical Neurosciences and Hotchkiss Brain Institute, Cumming School of Medicine University of Calgary Alberta Canada.ORCID 0000-0002-3466-496X
Jennifer S RabinDepartment of Medicine (Neurology), Sunnybrook Health Sciences Centre Toronto Ontario Canada.ORCID 0000-0003-4754-2221
Katie N DaintyInstitute of Health Policy, Management and Evaluation University of Toronto Ontario Canada.ORCID 0000-0002-2906-8813
Morgan BarenseDepartment of Psychology University of Toronto Ontario Canada.ORCID 0000-0002-4008-9201
Krista L LanctôtDepartment of Psychiatry and Department of Pharmacology and Toxicology, Temerty Faculty of Medicine University of Toronto Ontario Canada.ORCID 0000-0001-7024-6637
Aravind GaneshCalgary Stroke Program, Departments of Clinical Neurosciences and Community Health Sciences, the Hotchkiss Brain Institute, the Mathison Centre for Mental Health Research and Education, and the O'Brien Institute for Public Health University of Calgary Cumming School of Medicine Calgary Canada.ORCID 0000-0001-5520-2070
Richard H SwartzInstitute of Medical Science, University of Toronto Ontario Canada.ORCID 0000-0001-6571-5531

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCognitive impairment after stroke is common and associated with poorer outcomes. However, cognition is rarely assessed in acute or secondary prevention randomized controlled trials (RCTs), and those that do have not been systematically synthesized. This review examines how often cognitive end points are used, specific assessments applied, domains tested, and rates of missing cognitive data.

methodsWe performed a search on EMBASE, PsycINFO, MEDLINE and Cumulative Index to Nursing and Allied Health for RCTs involving adult (≥18 years) participants with stroke, published from 2011 to 2024. Abstracts and full-text publications were screened for stroke RCTs with cognitive end points. These were categorized into acute, secondary prevention, and rehabilitation trials. Descriptive statistics summarized the frequency of cognitive end points, domains, and missing data rates in acute and prevention trials.

resultsOf 12 822 screened studies, 980 met criteria for full-text screening and 406 were stroke RCTs with a cognitive end point. Among these, 43 were acute and secondary prevention RCTs eligible for data extraction. The Mini-Mental State Examination (22/43 studies, 52%) and Montreal Cognitive Assessment (18/43 studies, 42%) were used in the most RCTs. There were 66 distinct cognitive tasks used, with greatest diversity in memory tasks (19), executive tasks (11) and global screens (11). Mean missing data were 22.2% (SD: 10.4%, range 0%-62%).

conclusionsCognitive tasks are infrequent outcomes in stroke RCTs. When used, the tasks and domains assessed vary widely and are heavily affected by missing data. More pragmatic approaches to measuring meaningful cognitive change in all clinical trial participants are needed.

Indexed as

CognitionCognitive DysfunctionRandomized Controlled Trials as TopicSecondary PreventionStrokeStroke RehabilitationHumansMental Status and Dementia Testsacute strokecognitionoutcomesrandomized controlled trialsscalessecondary prevention

Identifiers

PMID40792595
PMCPMC12748075

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.