Effects of transcranial magnetic stimulation of the rostromedial prefrontal cortex in obsessive–compulsive disorder: a randomized clinical trial

New interventions are needed for obsessive-compulsive disorder. Here we present a randomized single-blinded, two-arm, parallel-group, sham-controlled clinical trial assessing the efficacy of prefrontal cortex stimulation in reducing obsessive-compulsive disorder symptoms and frontostriatal connectiv...

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Veröffentlicht in:Nature mental health 2023-08, Vol.1 (8), p.555-563
Hauptverfasser: Cocchi, Luca, Naze, Sebastien, Robinson, Conor, Webb, Lachlan, Sonkusare, Saurabh, Hearne, Luke J., Whybird, Genevieve, Saffron, Grace, Scott, Grace, Hall, Caitlin V., Nott, Zoie, Adsett, Jessica, Grasby, Katrina L., Jentjens, Joshua, Scott, James G., Marcus, Leo, Savage, Emma, Zalesky, Andrew, Burgher, Bjorn, Breakspear, Michael
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container_title Nature mental health
container_volume 1
creator Cocchi, Luca
Naze, Sebastien
Robinson, Conor
Webb, Lachlan
Sonkusare, Saurabh
Hearne, Luke J.
Whybird, Genevieve
Saffron, Grace
Scott, Grace
Hall, Caitlin V.
Nott, Zoie
Adsett, Jessica
Grasby, Katrina L.
Jentjens, Joshua
Scott, James G.
Marcus, Leo
Savage, Emma
Zalesky, Andrew
Burgher, Bjorn
Breakspear, Michael
description New interventions are needed for obsessive-compulsive disorder. Here we present a randomized single-blinded, two-arm, parallel-group, sham-controlled clinical trial assessing the efficacy of prefrontal cortex stimulation in reducing obsessive-compulsive disorder symptoms and frontostriatal connectivity (ACTRN12616001687482). Conducted at a single academic center, the trial enrolled participants diagnosed with obsessive-compulsive disorder who underwent baseline clinical assessments and neuroimaging. The intervention comprised 20 weekday sessions of neuronavigated continuous theta burst stimulation of the frontal pole or sham. Participants and all staff assessing intervention outcomes were blind to the conditions. We enrolled a sample of 50 individuals (26 active continuous theta burst stimulation) who completed the neuroimaging and clinical assessments at the primary 4 week endpoint. Clinical data at the secondary 6 month endpoint were obtained from 46 participants (23 active). Symptoms of obsessive-compulsive disorder (primary outcome) decreased in both groups (active −4.35, P 
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Here we present a randomized single-blinded, two-arm, parallel-group, sham-controlled clinical trial assessing the efficacy of prefrontal cortex stimulation in reducing obsessive-compulsive disorder symptoms and frontostriatal connectivity (ACTRN12616001687482). Conducted at a single academic center, the trial enrolled participants diagnosed with obsessive-compulsive disorder who underwent baseline clinical assessments and neuroimaging. The intervention comprised 20 weekday sessions of neuronavigated continuous theta burst stimulation of the frontal pole or sham. Participants and all staff assessing intervention outcomes were blind to the conditions. We enrolled a sample of 50 individuals (26 active continuous theta burst stimulation) who completed the neuroimaging and clinical assessments at the primary 4 week endpoint. Clinical data at the secondary 6 month endpoint were obtained from 46 participants (23 active). Symptoms of obsessive-compulsive disorder (primary outcome) decreased in both groups (active −4.35, P &lt; 0.001; sham −5.92, P &lt; 0.001), but there was no significant difference between groups (P = 0.33, ηp2 = 0.02). Likewise, there was no significant difference between groups in changes of frontal pole connectivity with the striatum (P = 0.09, ηp2 = 0.06). Changes in secondary outcomes (symptoms of anxiety and depression and localized frontal pole activity) did not differ between groups. Dropout rates did not vary between groups and the most common treatment-related adverse event in both groups was headache. Our findings suggest that frontal pole continuous theta burst stimulation is no different to sham in reducing obsessive-compulsive disorder symptoms. 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Symptoms of obsessive-compulsive disorder (primary outcome) decreased in both groups (active −4.35, P &lt; 0.001; sham −5.92, P &lt; 0.001), but there was no significant difference between groups (P = 0.33, ηp2 = 0.02). Likewise, there was no significant difference between groups in changes of frontal pole connectivity with the striatum (P = 0.09, ηp2 = 0.06). Changes in secondary outcomes (symptoms of anxiety and depression and localized frontal pole activity) did not differ between groups. Dropout rates did not vary between groups and the most common treatment-related adverse event in both groups was headache. Our findings suggest that frontal pole continuous theta burst stimulation is no different to sham in reducing obsessive-compulsive disorder symptoms. 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subjects Achievement tests
Medical imaging
Neuroimaging
Transcranial magnetic stimulation
title Effects of transcranial magnetic stimulation of the rostromedial prefrontal cortex in obsessive–compulsive disorder: a randomized clinical trial
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