Publication:
Psychomotor Slowing in Psychosis and Inhibitory Repetitive Transcranial Magnetic Stimulation: A Randomized Clinical Trial.

cris.virtual.author-orcid0000-0003-4026-3561
cris.virtual.author-orcid0000-0001-6007-8668
cris.virtual.author-orcid0000-0002-5221-5148
cris.virtualsource.author-orcid4dd58310-1e06-4649-a9b8-7de035422935
cris.virtualsource.author-orcidf18f2285-4893-495a-b279-f5208121ae42
cris.virtualsource.author-orciddb534c21-12d0-4e76-8081-2c8cab38642a
cris.virtualsource.author-orcid2dba01bf-2546-42b5-94b6-87c9c4f551af
cris.virtualsource.author-orcid96f155fc-9385-43c1-b112-8ee642dabecb
cris.virtualsource.author-orcid4b453cc2-3945-48d5-8989-b18f3456b833
cris.virtualsource.author-orcidfec7aa6c-23dd-47b1-a2d2-f68cfac1b7df
cris.virtualsource.author-orcid6a25fbec-1af7-4b1f-9842-abcbb461575b
cris.virtualsource.author-orcida50989ae-a263-4c15-851d-7466d58876ac
datacite.rightsopen.access
dc.contributor.authorWalther, Sebastian
dc.contributor.authorAlexaki, Despoina Danai
dc.contributor.authorWeiss, Florian
dc.contributor.authorBaumann Gama, Daniel Eduardo
dc.contributor.authorKyrou, Alexandra
dc.contributor.authorNuoffer, Melanie Gabriela
dc.contributor.authorWüthrich, Florian
dc.contributor.authorLefebvre, Stéphanie
dc.contributor.authorNadesalingam, Niluja
dc.date.accessioned2024-10-26T17:26:38Z
dc.date.available2024-10-26T17:26:38Z
dc.date.issued2024-06-01
dc.description.abstractIMPORTANCE Psychomotor slowing is a frequent symptom of psychosis, impairing gross and fine motor behavior. It is associated with poor outcomes and functioning, and no treatment is available. OBJECTIVE To investigate whether 15 sessions of inhibitory repetitive transcranial magnetic stimulation (rTMS) may reduce psychomotor slowing. DESIGN, SETTING, AND PARTICIPANTS This was a 4-arm, double-blind, randomized, sham-controlled trial at a university hospital in Switzerland. Enrollment took place from March 2019 to August 2022. Adults aged 18 to 60 years with schizophrenia spectrum disorders and severe psychomotor slowing were eligible. All patients continued existing medications, including antipsychotics and benzodiazepines. Those with substance misuse (other than nicotine), conditions associated with impaired or aberrant movement, convulsions, history of hearing problems, other conditions typically excluded from magnetic resonance imaging or TMS, any TMS treatment in the past 3 months, or those who were pregnant or breastfeeding were excluded. Of 615 patients screened for eligibility, 103 were randomized and 88 received at least 1 session of rTMS: 22 were assigned to 1-Hz rTMS, 22 to iTBS, 22 to sham, and 22 to the waiting group. Follow-up was conducted at 6 weeks and 24 weeks following the week 3 assessments including clinical, functional, and motor measures. INTERVENTIONS Fifteen sessions of rTMS in 3 weeks over the supplementary motor area: 1-Hz rTMS, iTBS, sham, or no treatment (waiting). After 3 weeks, the waiting group received 15 sessions of 1-Hz rTMS over the supplementary motor area. MAIN OUTCOMES AND MEASURES The main outcome was the proportion of responders at week 3 in the Salpêtrière Retardation Rating Scale (SRRS) defined as a 30% or greater reduction from baseline (last-observation-carried-forward). The SRRS has 15 items and a maximum total score of 60. RESULTS Of the 88 participants analyzed, 45 were men and 43 were women. The mean (SD) age was 36.3 (12.4) years and the mean (SD) SRRS score was 24.0 (5.9). A total of 69 participants completed the study. At week 3, response rates differed between groups: 15 of 22 (68%) in the 1-Hz rTMS group, 8 of 22 (36%) in the iTBS group, 7 of 22 (32%) in the sham group, and 4 of 22 (18%) in the waiting group (χ23 = 12.1; P = .007). The 1-Hz rTMS group had more responders than sham (odds ratio [OR], 0.13; 95% CI, 0.02-0.65; P = .03), iTBS (OR, 0.12; 95% CI, 0.02-0.61; P = .02), and waiting (OR, 0.04; 95% CI, 0.01-0.22; P = .003). In the waiting group, 10 of 16 participants (63%) responded after receiving 15 sessions of 1-Hz rTMS. No serious adverse events occurred. CONCLUSIONS AND RELEVANCE In this study, inhibitory add-on rTMS safely alleviated psychomotor slowing in psychosis compared with iTBS, sham, and no treatment. The treatment was also effective with delayed onset. Future studies need to explore the neural changes associated with supplementary motor area rTMS in psychosis. TRIAL REGISTRATION ClinicalTrials.gov Identifier: NCT03921450.
dc.description.numberOfPages9
dc.description.sponsorshipZentrum für Translationale Forschung der Universitätsklinik für Psychiatrie und Psychotherapie
dc.description.sponsorshipUniversitätsklinik für Psychiatrie und Psychotherapie (PP)
dc.identifier.doi10.48350/193603
dc.identifier.pmid38416468
dc.identifier.publisherDOI10.1001/jamapsychiatry.2024.0026
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/175014
dc.language.isoen
dc.publisherAmerican Medical Association
dc.relation.ispartofJAMA psychiatry
dc.relation.issn2168-622X
dc.relation.organizationZentrum für Translationale Forschung der Universitätsklinik für Psychiatrie und Psychotherapie
dc.relation.organizationUniversity Hospital of Psychiatry and Psychotherapy
dc.relation.schoolGraduate School for Health Sciences (GHS)
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titlePsychomotor Slowing in Psychosis and Inhibitory Repetitive Transcranial Magnetic Stimulation: A Randomized Clinical Trial.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.endPage571
oaire.citation.issue6
oaire.citation.startPage563
oaire.citation.volume81
oairecerif.author.affiliationZentrum für Translationale Forschung der Universitätsklinik für Psychiatrie und Psychotherapie
oairecerif.author.affiliationUniversitätsklinik für Psychiatrie und Psychotherapie (PP)
oairecerif.author.affiliationUniversitätsklinik für Psychiatrie und Psychotherapie (PP)
oairecerif.author.affiliationUniversitätsklinik für Psychiatrie und Psychotherapie (PP)
oairecerif.author.affiliationUniversitätsklinik für Psychiatrie und Psychotherapie (PP)
oairecerif.author.affiliationZentrum für Translationale Forschung der Universitätsklinik für Psychiatrie und Psychotherapie
oairecerif.author.affiliationZentrum für Translationale Forschung der Universitätsklinik für Psychiatrie und Psychotherapie
oairecerif.author.affiliationZentrum für Translationale Forschung der Universitätsklinik für Psychiatrie und Psychotherapie
oairecerif.author.affiliationZentrum für Translationale Forschung der Universitätsklinik für Psychiatrie und Psychotherapie
oairecerif.author.affiliation2Universitätsklinik für Psychiatrie und Psychotherapie (PP)
oairecerif.author.affiliation2Zentrum für Translationale Forschung der Universitätsklinik für Psychiatrie und Psychotherapie
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unibe.date.licenseChanged2024-03-06 08:52:06
unibe.description.ispublishedpub
unibe.eprints.legacyId193603
unibe.journal.abbrevTitleJAMA Psychiatry
unibe.refereedtrue
unibe.subtype.articlejournal

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