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Study identifier: NCT06534684 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

The Cerebral and Cognitive Changes After Intermittent Theta Burst Stimulation (iTBS) Treatment for Depression

Condition: Depression, Unipolar · Depression Moderate  ·  Sponsor: University Hospital of North Norway

PhaseNA
Planned participants50
Who can joinAll sexes, 22 Years to 65 Years
Healthy volunteersNo

About this study

The present project aims to assess the neurocognitive impact of a two-week once-a-day regimen of intermittent theta burst stimulation (iTBS) compared to sham iTBS, when targeting the left dorsolateral prefrontal cortex (LDLPFC) in clinically depressed outpatients. The study investigates the relationships between changes in cerebral measures and cognitive performance on an N-back task in relation to the antidepressive effect following iTBS.

This description comes directly from the study's public registry record.

Talk to the study team

Per M Aslaksen, PhD  ·  77649234  ·  per.aslaksen@unn.no

Marte C Ørbo, PhD  ·  77645333  ·  marte.c.orbo@uit.no

Always discuss trial participation with your own doctor first.

Locations (1)

University Hospital North NorwayTromsø, NorwayRecruiting

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Source record: clinicaltrials.gov/study/NCT06534684