Evidence map›Paper›PMID 38228914›Full record

Trial reportNature medicine2024

Connectivity-guided intermittent theta burst versus repetitive transcranial magnetic stimulation for treatment-resistant depression: a randomized controlled trial.

Richard Morriss, Paul M Briley, Lucy Webster, Mohamed Abdelghani, Shaun Barber, Peter Bates, Cassandra Brookes, Beth Hall, Luke Ingram, Micheal Kurkar and 8 more

Open access · hybridAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Nature medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
21.8field-weighted citation impact, top 1% of its field
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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 88 citations in OpenAlex.

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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

18 authors at 8 institutions in 1 country.

Richard MorrissMental Health and Clinical Neurosciences, School of Medicine, University of Nottingham, Nottingham, UK. richard.morriss@nottingham.ac.uk.ORCID 0000-0003-2910-4121
Paul M BrileyMental Health and Clinical Neurosciences, School of Medicine, University of Nottingham, Nottingham, UK.ORCID 0000-0002-5372-6505
Lucy WebsterInstitute of Mental Health, Nottinghamshire Healthcare NHS Foundation Trust, Nottingham, UK.
Mohamed AbdelghaniClinical Neuromodulation Service, Camden and Islington NHS Foundation Trust, London, UK.ORCID 0000-0002-9888-6588
Shaun BarberLeicester Clinical Trials Unit, University of Leicester, Leicester, UK.
Peter BatesInstitute of Mental Health, Nottinghamshire Healthcare NHS Foundation Trust, Nottingham, UK.ORCID 0000-0002-0558-6907
Cassandra BrookesLeicester Clinical Trials Unit, University of Leicester, Leicester, UK.
Beth HallCumbria, Northumberland, Tyne and Wear NHS Foundation Trust, Newcastle upon Tyne, UK.ORCID 0000-0002-5812-3121
Luke IngramLeicester Clinical Trials Unit, University of Leicester, Leicester, UK.ORCID 0000-0001-5711-7400
Micheal KurkarPennine Care TMS Service, Pennine Care NHS Foundation Trust, Oldham, UK.
Sudheer LankappaInstitute of Mental Health, Nottinghamshire Healthcare NHS Foundation Trust, Nottingham, UK.
Peter F LiddleMental Health and Clinical Neurosciences, School of Medicine, University of Nottingham, Nottingham, UK.ORCID 0000-0001-6473-7640
R Hamish McAllister-WilliamsNorthern Centre for Mood Disorders, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
Alexander O'Neil-KerrCentre for Neuromodulation, Northamptonshire Healthcare NHS Foundation Trust, Northampton, UK.
Stefan PszczolkowskiMental Health and Clinical Neurosciences, School of Medicine, University of Nottingham, Nottingham, UK.
Ana Suazo Di PaolaLeicester Clinical Trials Unit, University of Leicester, Leicester, UK.
Yvette WaltersLeicester Clinical Trials Unit, University of Leicester, Leicester, UK.
Dorothee P AuerMental Health and Clinical Neurosciences, School of Medicine, University of Nottingham, Nottingham, UK.ORCID 0000-0002-4745-3635
University of Leicester · GBUniversity of Nottingham · GBNottinghamshire Healthcare NHS Foundation Trust · GBCamden and Islington NHS Foundation Trust · GBCumbria Northumberland Tyne and Wear NHS Foundation Trust · GBNewcastle University · GBNorthamptonshire Healthcare NHS Foundation Trust · GBPennine Care NHS Foundation Trust · GB

Funding

DH | National Institute for Health Research (NIHR) 16/44/22
6 · The paper itself

Abstract

Disruption in reciprocal connectivity between the right anterior insula and the left dorsolateral prefrontal cortex is associated with depression and may be a target for neuromodulation. In a five-center, parallel, double-blind, randomized controlled trial we personalized resting-state functional magnetic resonance imaging neuronavigated connectivity-guided intermittent theta burst stimulation (cgiTBS) at a site based on effective connectivity from the right anterior insula to the left dorsolateral prefrontal cortex. We tested its efficacy in reducing the primary outcome depression symptoms measured by the GRID Hamilton Depression Rating Scale 17-item over 8, 16 and 26 weeks, compared with structural magnetic resonance imaging (MRI) neuronavigated repetitive transcranial magnetic stimulation (rTMS) delivered at the standard stimulation site (F3) in patients with 'treatment-resistant depression'. Participants were randomly assigned to 20 sessions over 4-6 weeks of either cgiTBS (n = 128) or rTMS (n = 127) with resting-state functional MRI at baseline and 16 weeks. Persistent decreases in depressive symptoms were seen over 26 weeks, with no differences between arms on the primary outcome GRID Hamilton Depression Rating Scale 17-item score (intention-to-treat adjusted mean, -0.31, 95% confidence interval (CI) -1.87, 1.24, P = 0.689). Two serious adverse events were possibly related to TMS (mania and psychosis). MRI-neuronavigated cgiTBS and rTMS were equally effective in patients with treatment-resistant depression over 26 weeks (trial registration no. ISRCTN19674644).

Indexed as

Depressive Disorder, Treatment-ResistantTranscranial Magnetic StimulationDouble-Blind MethodHumansMagnetic Resonance ImagingPrefrontal CortexTreatment Outcome

Identifiers

PMID38228914
PMCPMC10878976
OpenAlexW4390912825

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.