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ArticleBMC psychiatry2025

CATATOnia treatment with transcranial direct current electrostimulation: protocol of a randomised, double-blind, placebo-controlled bicentric superiority study (CATATOES).

Mylène Moyal, David Attali, Alice Le Berre, Noomane Bouaziz, Anton Iftimovici, François Ramon, Adèle Henensal, Louise Dahan, Laetitia Canivet, Ghita Dadi and 14 more

Registry-linked trialAbstract 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. It is linked to trial NCT06139432 (Catatonia), which is not on this 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.

NCT06139432 naunknown statusnot on this map

Catatonia: Effectiveness of Transcranial Direct Current Electrostimulation (CATATOES)

TypeinterventionalSponsorCentre Hospitalier St AnneRan2023 to 2025Enrolled70ConditionsCatatoniaArmsActive tDCS, Sham tDCS
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

24 authors.

Mylène MoyalGHU-Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, Paris, F-75014, France. m.moyal@ghu-paris.fr.
David AttaliGHU-Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, Paris, F-75014, France.
Alice Le BerreGHU-Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, Paris, F-75014, France.
Noomane BouazizEPS ville Evrard 93G03, Neuilly-sur- Marne, 93330, France.
Anton IftimoviciGHU-Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, Paris, F-75014, France.
François RamonInstitute of Psychiatry and Neuroscience of Paris (IPNP), Université Paris Cité, INSERM U1266, Paris, 75014, France.
Adèle HenensalGHU-Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, Paris, F-75014, France.
Louise DahanInstitute of Psychiatry and Neuroscience of Paris (IPNP), Université Paris Cité, INSERM U1266, Paris, 75014, France.
Laetitia CanivetGHU-Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, Paris, F-75014, France.
Ghita DadiGHU-Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, Paris, F-75014, France.
Clément DebackerGHU-Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, Paris, F-75014, France.
Maliesse LuiGHU-Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, Paris, F-75014, France.
Sylvain CharronInstitute of Psychiatry and Neuroscience of Paris (IPNP), Université Paris Cité, INSERM U1266, Paris, 75014, France.
Anaëlle AlouitInstitute of Psychiatry and Neuroscience of Paris (IPNP), Université Paris Cité, INSERM U1266, Paris, 75014, France.
Khaoussou SyllaGHU-Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, Paris, F-75014, France.
Rossella Letizia MancusiGHU-Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, Paris, F-75014, France.
Thierry GallardaGHU-Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, Paris, F-75014, France.
Arnaud CachiaInstitute of Psychiatry and Neuroscience of Paris (IPNP), Université Paris Cité, INSERM U1266, Paris, 75014, France.
Martine GavaretGHU-Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, Paris, F-75014, France.
Boris ChaumetteGHU-Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, Paris, F-75014, France.
Catherine OppenheimGHU-Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, Paris, F-75014, France.
Dominique JanuelEPS ville Evrard 93G03, Neuilly-sur- Marne, 93330, France.
Marion Plaze *GHU-Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, Paris, F-75014, France.
Alexandre Haroche *GHU-Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, Paris, F-75014, France.

Funding

Starting GRANT 2020 GHU Paris Psychiatrie et Neurosciences Starting GRANT 202
6 · The paper itself

Abstract

backgroundCatatonia is a severe psychomotor syndrome with high morbidity and mortality. Lorazepam and electroconvulsive therapy (ECT) are the main recommended treatments. Lorazepam-resistant catatonia accounts for about 30% of cases, particularly in neurodevelopmental disorders. ECT is crucial in these situations but faces challenges of tolerability and accessibility. Transcranial direct current stimulation (tDCS), a promising intervention, is emerging as a non-invasive, cost-effective neurostimulation tool and has demonstrated efficacy and safety in case reports and small series of catatonic patients (N < 10). The CATATOES study aims to assess the efficacy and safety of tDCS using a randomised, double-blind, placebo-controlled, bicentric superiority trial involving 70 patients with catatonia. Secondary objectives aim to highlight the mechanism of action of tDCS and to explore the pathophysiology of catatonia.

methodsSeventy participants with lorazepam-resistant catatonia will undergo 20 sessions of active or sham tDCS, administered twice daily at two mA for 20 min, with anodal stimulation in the left dorsolateral prefrontal cortex (DLPFC) and cathodal stimulation in the left temporoparietal junction (TPJ). In addition to daily clinical assessment, patients will undergo (i) structural, functional and diffusion magnetic resonance imaging (MRI), (ii) 64-channel resting state electroencephalogram (EEG), and (iii) blood test with inflammatory, neurogenesis and genetic markers, before, during and after the treatment course. DISCUSSION:  Catatonia is in critical need of therapeutic improvement. We anticipate that this study will pave the way for the routine use of tDCS in the treatment of lorazepam-resistant catatonia, ultimately contributing to a reduction of morbidity, mortality, and associated costs of catatonia. ClinicalTrials.gov Identifier NCT06139432; Registration date 11/24/2023.

Indexed as

CatatoniaTranscranial Direct Current StimulationAdultDorsolateral Prefrontal CortexDouble-Blind MethodEquivalence Trials as TopicFemaleHumansLorazepamMagnetic Resonance ImagingMaleMiddle AgedMulticenter Studies as TopicRandomized Controlled Trials as TopicTreatment OutcomeLorazepamCatatonic syndromeEEGGeneticMRINeuroinflammationNeuromodulationTDCS

Identifiers

PMID41062970
PMCPMC12506329

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Registered trials

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