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

cTBS/fMRI Study of Hierarchical Control in the PFC

Transcranial Magnetic Stimulation

Enrolled (actual)
39
Serious AEs
0.0%
Results posted
Jun 2025
Primary outcome: Primary: PFC-PPC Effective Connectivity — 0.3646; 0.3756; 0.3425; 0.4519 Hertz — p=0.5736

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
Apr 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
PFC-PPC Effective Connectivity
0.3646; 0.3756; 0.3425; 0.4519; 0.466; 0.4004 0.5736
PRIMARY
PFC-PPC Activation
0.1132; 0.1155; 0.0992; 0.1519; 0.1619; 0.162 0.8152
SECONDARY
Temporal Control Performance (Error Rate)
4.541; 3.826; 4.329; -0.293; -0.942; 0.358 0.9504
SECONDARY
Contextual Control Performance (Error Rate)
5.580; 6.950; 5.890; 1.990; 2.960; 2.700 0.0266 sig
SECONDARY
Temporal x Contextual Control Performance (Error Rate)
-1.810; 0.082; -2.181; 1.270; 1.141; 1.400 0.0091 sig
SECONDARY
Temporal Control Performance (Reaction Time)
15.700; 11.987; -2.244; -18.172; -16.540; -23.348 0.0211 sig
SECONDARY
Contextual Control Performance (Reaction Time)
197.700; 185.443; 160.900; 163.774; 146.982; 132.500 0.0344 sig
SECONDARY
Temporal Control x Contextual Control Performance (Reaction Time)
55.600; 53.162; 53.280; 141.900; 131.227; 125.100 0.0189 sig

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 (NCT04464473). 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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