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WithdrawnNo phase

NeuroControl of Nicotine Dependence

Key facts

Who runs it
University of Missouri-Columbia
Where
Columbia, United StatesSee the site
Trial code
Status
Withdrawn
Started
1 Oct 2024
Expected to end
30 Apr 2030
Type of study
Interventional, 3 groups
Treatments tested
  • Repetitive Transcranial Magnetic Stimulation (rTMS)
Record updated
9 October 2026
Why it stopped
Funding

Who can take part

Age
18 years to 60 years
Sex
Women and men
Healthy volunteers
Can take part

The registry criteria, word for word

Show all 14 criteriaShow less

Who can take part

  • Nicotine Dependence as measured by: Smoke ≥ 8 cigarettes/day for ≥ 2 yrs, expired carbon monoxide (CO) concentration of ≥ 10 ppm, positive urine cotinine test and FTND score ≥ 3 Or ≥ 15 uses of electronic cigarette/day for ≥ 1 year, positive urine cotinine test, and PS-ECDI score ≥ 3
  • English Fluency
  • Functional Vision (with corrective lenses as needed)

Who cannot take part

  • Use of psychotropic and antiepileptic medications in the last month
  • Electroconvulsive therapy in the past 6 months
  • Presence of an untreated illness or serious medical condition
  • History of major neurological illness
  • Contraindication to TMS (history of neurological disorder or seizure, increased intracranial pressure, brain surgery, or head trauma with loss of consciousness for >15 min., implanted electronic device, metal in the head) or MRI
  • Any use of substances that lower seizure threshold
  • Unstable cardiac disease or hypertension, severe renal or liver insufficiency, or sleep apnea
  • Current or past psychosis
  • BAC greater than 0.0
  • Positive urine pregnancy test
  • Any other concern that in the investigator's opinion would impact participant safety, study instruction compliance, or confound the interpretation of the study results

Where in United States

  • Health Neuroscience CenterColumbia, United States

About the trial

What the trial wants to find out

The purpose of the study is to examine the effects of continuous theta burst stimulation (cTBS) on different forms of cognitive control in adults who smoke cigarettes, and to determine if the location where cTBS is delivered may help smokers reduce or quit smoking. Participation in the study will take 3-weeks over 4 visits, with a total time commitment of approximately 12 hours.

The 3 groups in the trial

  • cTBS to Ventrolateral Prefrontal CortexTreatment being tested

    Continuous theta-burst stimulation (cTBS), a form of repetitive transcranial magnetic stimulation (rTMS), affects brain areas stimulated directly underneath the scalp and brain areas that are functionally connected. cTBS will be applied to the ventrolateral prefrontal cortex.

    Treatment: Repetitive Transcranial Magnetic Stimulation (rTMS)

  • cTBS to Dorsomedial Prefrontal CortexTreatment being tested

    Continuous theta-burst stimulation (cTBS), a form of repetitive transcranial magnetic stimulation (rTMS), affects brain areas stimulated directly underneath the scalp and brain areas that are functionally connected. cTBS will be applied to the dorsomedial prefrontal cortex.

    Treatment: Repetitive Transcranial Magnetic Stimulation (rTMS)

  • cTBS to VertexTreatment being tested

    Continuous theta-burst stimulation (cTBS), a form of repetitive transcranial magnetic stimulation (rTMS), affects brain areas stimulated directly underneath the scalp and brain areas that are functionally connected. cTBS will be applied to the vertex.

    Treatment: Repetitive Transcranial Magnetic Stimulation (rTMS)

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Neuronavigated Non-invasive Brain Stimulation for Nicotine Dependence.
Record updated
9 October 2026