Evidence map›Paper›PMID 41922053›Full record

SynthesisBMJ open2026

Sex and gender reporting and differences in trials evaluating patient decision aids: a secondary analysis of systematic review with meta-analysis.

Dawn Stacey, France Légaré, Krystina B Lewis, Maureen Smith, Meg E Carley, Michael J Barry, Carol Bennett, Paulina Bravo, Karina Dahl Steffensen, Jeanette Finderup and 9 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in BMJ open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

19 authors.

Dawn StaceyUniversity of Ottawa School of Nursing, Ottawa, Ontario, Canada dstacey@uottawa.ca.ORCID http://orcid.org/0000-0002-2681-741X
France LégaréDepartment of Family Medicine and Emergency Medicine, Universite Laval, Quebec, Quebec, Canada.ORCID http://orcid.org/0000-0002-2296-6696
Krystina B LewisUniversity of Ottawa School of Nursing, Ottawa, Ontario, Canada.
Maureen SmithCochrane Collaboration Consumer Network, Ottawa, Ontario, Canada.
Meg E CarleyCentre for Implementation Research, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.ORCID http://orcid.org/0000-0003-2334-0908
Michael J BarryDepartment of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
Carol BennettMethodological and Implementation Research, The Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Paulina BravoInstituto Oncológico Fundación Arturo López Pérez, Providencia, Chile.ORCID http://orcid.org/0000-0001-7378-6487
Karina Dahl SteffensenAalborg University The Faculty of Medicine, Aalborg, North Denmark Region, Denmark.ORCID http://orcid.org/0000-0002-9217-3907
Jeanette FinderupDepartment of Renal Medicine, Aarhus University Hospital, Aarhus, Central Denmark Region, Denmark.
Yulia GendlerDepartment of Nursing, Ariel University School of Health Sciences, Ari'el, Israel.ORCID http://orcid.org/0000-0001-9958-7777
Amédé GogovorDepartment of Family Medicine and Emergency Medicine, Université Laval, Québec City, Quebec, Canada.
Janet GundersonCochrane Collaboration Consumer Network, Glaslyn, Saskatchewan, Canada.
Shannon E KellyUniversity of Ottawa Heart Institute, Ottawa, Ontario, Canada.
Lissa Pacheco-BrousseauUniversity of Ottawa School of Rehabilitation Sciences, Ottawa, Ontario, Canada.
Logan TrenamanUniversity of Washington, Seattle, Washington, USA.ORCID http://orcid.org/0000-0002-6399-5741
Lyndal TrevenaSydney University Medical Society, Camperdown, New South Wales, Australia.ORCID http://orcid.org/0000-0003-1419-1832
Robert J VolkThe University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Ian D GrahamSchool of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesPatient decision aids (PtDAs) are effective interventions to support patient involvement in health decisions and have the potential to impact favourably on health inequities by reducing gender bias in clinical practice. The aim was to explore sex and gender reporting and differences in randomised controlled trials (RCTs) evaluating PtDAs for adults making treatment or screening decisions.

designSecondary analysis of the Cochrane review of PtDAs of RCTs that reported sex and/or gender. The original review searched MEDLINE, Embase, PsychINFO and EBSCO from journal inception to March 2022. Two team members independently screened citations, extracted data and assessed risk of bias. For this secondary analysis, we only included primary outcomes from the original review. We assessed appropriate use of terminology for sex (biological attribute) and gender (social construct). When terms were used interchangeably, it was considered inaccurate. Findings were synthesised descriptively, and we used meta-analysis when two or more RCTs were conducted with females/women or males/men using similar outcome measures. PRIMARY AND SECONDARY OUTCOME MEASURES: Informed values-choice congruence and the quality of the decision-making process (eg, knowledge, accurate risk perceptions, feeling informed, clear values, participation in decision making, undecided) and adverse events (eg, decision regret, emotional distress) by sex and gender.

resultsOf 209 RCTs in the original review, 206 reported sex and/or gender, with 35 (17%) using accurate terminology. Of 206 RCTs, 70 were with females/women only, 27 males/men only, 12 analysed by sex/gender and 97 RCTs did not disaggregate findings by sex or gender. Meta-analysis comparing RCTs for females/women to usual care and RCTs for males/men only compared with usual care showed similar mean differences in knowledge scores (10.84 vs 9.38 out of 100; p=0.44). Males/men had significantly higher self-reported participation in decision making compared with females/women (RR 3.16 vs 0.95; p<0.01). Meta-analysis showed no significant differences in other outcomes.

conclusionsIn PtDA RCTs, sex and gender terms are used interchangeably and 6% analysed outcomes by sex or gender. Meta-analysis of males/men only given PtDAs showed higher self-reported decision making participation in clinical practice compared to usual care versus females/women only compared with usual care. Researchers must improve reporting sex and gender in PtDA RCTs to assess how it influences health inequities.

Indexed as

Decision MakingDecision Support TechniquesPatient ParticipationFemaleHumansMaleRandomized Controlled Trials as TopicSecondary Data AnalysisSex FactorsClinical Decision-MakingHealth EquityKnowledgeMeta-AnalysisPatient-Centered CareSystematic Review

Identifiers

PMID41922053
PMCPMC13052785

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.