Evidence map›Paper›PMID 42766584›Full record

ArticlePloS one2026

Exploring sex-specific symptom trajectories in psychosis following metacognitive training (MCT): Evidence from a large-scale retrospective harmonized database.

Maria Lamarca, Adrien Goncalves, Steffen Moritz, Łukasz Gawęda, Vanessa Acuña, Caroline König, Fabrice Berna, Susana Ochoa

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

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Maria LamarcaParc Sanitari Sant Joan de Déu, Sant Boi de Llobregat, Barcelona, Spain.ORCID https://orcid.org/0009-0009-6426-560X
Adrien GoncalvesUniversity of Strasbourg, Inserm, UMR_S 1329, Strasbourg, France.ORCID https://orcid.org/0009-0000-4834-3043
Steffen MoritzDepartment of Psychiatry and Psychotherapy, University Medical Center Hamburg, Hamburg, Germany.
Łukasz GawędaExperimental Psychopathology Lab, Institute of Psychology, Polish Academy of Sciences, Warsaw, Poland.
Vanessa AcuñaDepartamento de Psiquiatría, Escuela de Medicina, Facultad de Medicina, Universidad de Valparaíso, Valparaíso, Chile.
Caroline KönigSoft Computing Research Group at Intelligent Data Science and Artificial Intelligence Research Center, Center Universitat Politècnica de Catalunya, Barcelona, Spain.ORCID https://orcid.org/0000-0002-7543-8686
Fabrice BernaUniversity of Strasbourg, Inserm, UMR_S 1329, Strasbourg, France.
Susana OchoaParc Sanitari Sant Joan de Déu, Sant Boi de Llobregat, Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sex-related differences in the clinical presentation and course of schizophrenia spectrum disorders are increasingly recognized, yet it remains unclear whether biological sex moderates response to psychological interventions. Metacognitive Training for psychosis is an evidence-based psychological intervention targeting cognitive biases associated with psychotic symptoms, but evidence regarding sex-specific treatment effects remain limited. The present study examined whether biological sex influences symptom trajectories following Metacognitive Training in individuals with schizophrenia spectrum disorders. We analyzed harmonized retrospective data from an international consortium (PERMEPSY) including participants who received Metacognitive Training for psychosis in routine clinical or research settings. The sample comprised 573 participants diagnosed with schizophrenia spectrum disorders across different stages of illness. Control group data was not available due to the retrospective nature of the data and a lack of a standardised control group among included datasets. Psychotic symptoms were assessed using the Positive and Negative Syndrome Scale, including positive, negative, general, and total symptom scores. Repeated-measures analyses of variance were conducted to examine the effects of time, sex, and their interaction on symptom change. Across the full sample, Metacognitive Training for psychosis was associated with significant reductions in positive, negative, general, and overall psychotic symptoms. However, no significant moderation of symptom change by biological sex was detected, indicating comparable symptom improvement in males and females across all symptom domains. These findings are consistent with prior evidence supporting MCT as a broadly applicable psychological intervention for psychosis, with comparable symptom changes observed in males and females following treatment. Although sex-related differences in baseline symptom profiles were observed, biological sex did not influence the trajectory of symptom change following treatment. These results support the generalizability of Metacognitive Training and point to the relevance of examining more nuanced sex-related factors in future research.

Indexed as

MetacognitionPsychotic DisordersSchizophreniaAdultDatabases, FactualFemaleHumansMaleMiddle AgedRetrospective StudiesSex CharacteristicsSex FactorsYoung Adult

Identifiers

PMID42766584
PMCPMC13592629

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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.