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N/A N=39 Randomized Single-blind Basic Science

iTBS/fMRI Study of Hierarchical Control in the PFC

Transcranial Magnetic Stimulation

Enrolled (actual)
39
Serious AEs
0.0%
Results posted
Feb 2026
Primary outcome: Primary: PFC-PPC Effective Connectivity — 0.2177; 0.2248; 0.1911; 0.3157 Hertz — p=0.599

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
transcranial magnetic stimulation (Device)
Age
Adult · 18+ yrs
Sex
All
Sponsor
Florida State University
Primary completion
Dec 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
PFC-PPC Effective Connectivity
0.2177; 0.2248; 0.1911; 0.3157; 0.3168; 0.3153 0.599
PRIMARY
PFC-PPC Activation
0.1649; 0.174; 0.1721; 0.0796; 0.0958; 0.1021 0.083
SECONDARY
Temporal Control Performance (Error Rate)
3.6774; 4.6272; 3.9773; -0.9785; 0.0688; -0.7576 0.788
SECONDARY
Contextual Control Performance (Error Rate)
7.7178; 4.7408; 5.7449; 2.5568; 2.3794; 2.399 0.119
SECONDARY
Temporal x Contextual Control Performance (Error Rate)
-0.2367; -0.4449; -0.5051; 2.5568; 2.0457; 2.5884 0.985
SECONDARY
Temporal Control Performance (Reaction Time)
14.7162; 1.3866; 2.3381; -49.5445; -49.5869; -65.4566 0.567
SECONDARY
Contextual Control Performance (Reaction Time)
223.8835; 196.5144; 207.0607; 185.165; 151.2204; 172.9899 0.078
SECONDARY
Temporal x Contextual Control Performance (Reaction Time)
73.9891; 62.1515; 73.5031; 174.2524; 157.9577; 161.0199 0.621

Summary

The objective of this study is to examine the effect of transcranial magnetic stimulation (TMS) on the prefrontal cortex and posterior parietal cortex.

Eligibility Criteria

Inclusion Criteria

  • Between the ages of 18 and 30
  • Right-handed
  • Native English speaker or fluent by the age of 6

Exclusion Criteria

  • History of psychiatric disorders
  • History of neurological disorders
  • Receiving medications for psychiatric or neurological disorders
  • Familial history of epilepsy
  • Taking any drugs or medications that are pro-epileptic
  • Metal anywhere in the head excluding the mouth
  • Tinnitus
  • Women who are pregnant
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05878080). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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