Evidence map›Paper›PMID 40133861›Full record

ArticleBMC psychiatry2025

Using personalised brain stimulation to modulate social cognition in adults with autism-spectrum-disorder: protocol for a randomised single-blind rTMS study.

Katia Ourania Brouzou, Daniel Kamp, Lukas Hensel, Jana Lüdtke, Juha M Lahnakoski, Juergen Dukart, Nace Mikus, Christoph Mathys, Simon B Eickhoff, Leonhard Schilbach

Abstract readClinical Trial Protocol
In one paragraph

Article in BMC psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Katia Ourania Brouzou *Department of Psychiatry and Psychotherapy, Medical Faculty, Heinrich Heine University Düsseldorf, Düsseldorf, Germany. KatjaOurania.Brouzou@lvr.de.
Daniel Kamp *Department of Psychiatry and Psychotherapy, Medical Faculty, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Lukas HenselDepartment of Psychiatry and Psychotherapy, Medical Faculty, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Jana LüdtkeDepartment of Psychiatry and Psychotherapy, Medical Faculty, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Juha M LahnakoskiInstitute of Systems Neuroscience, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Juergen DukartInstitute of Systems Neuroscience, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Nace MikusInteracting Minds Centre, Aarhus University, Aarhus, Denmark.
Christoph MathysInteracting Minds Centre, Aarhus University, Aarhus, Denmark.
Simon B EickhoffInstitute of Systems Neuroscience, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Leonhard SchilbachDepartment of General Psychiatry 2, LVR-Klinikum Düsseldorf, Düsseldorf, Germany. leonhard.schilbach@lvr.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAutism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by impairments of social interaction and communication as well as repetitive, stereotyped behaviour. Previous research indicates that ASD without intellectual impairment is associated with underactivity and reduced functional connectivity of the brain's mentalizing pathway, to which the right temporo-parietal junction (rTPJ) serves as an important entry point and hub. In this study, we aim to utilize functional magnetic resonance imaging (fMRI) to localize activation maxima in the rTPJ and other regions involved in social cognition to generate individualized targets for neuro-navigated, intermittent theta burst stimulation (iTBS) in order to modulate brain activity in a region centrally engaged in social information processing.

methodsIn this single-blind, randomized, between-subject neuroimaging-guided brain stimulation study we plan to recruit 52 participants with prediagnosed ASD and 52 controls without ASD aged between 18 and 65 years. Participants will be classified into two groups and will randomly receive one session of either verum- or sham-iTBS. Effects will be assessed by using well-established experimental tasks that interrogate social behaviour, but also use computational modelling to investigate brain stimulation effects at this level. DISCUSSION: This study aims to use personalized, non-invasive brain stimulation to alter social information processing in adults with and without high-functioning ASD, which has not been studied before with a similar protocol or a sample size of this magnitude. By doing so in combination with behavioural and computational tasks, this study has the potential to provide new mechanistic insights into the workings of the social brain.

trial registrationGerman Clinical Trial Register, DRKS-ID: DRKS00028819. Registered 14 June 2022.

Indexed as

Autism Spectrum DisorderSocial CognitionTranscranial Magnetic StimulationAdolescentAdultAgedBrainFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedParietal LobeRandomized Controlled Trials as TopicSingle-Blind MethodTemporal LobeAutism spectrum disorderPersonalized neuronavigationSocial cognitionTranscranial magnetic stimulation

Identifiers

PMID40133861
PMCPMC11938784

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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.