Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
Healthy Volunteers
NCT06347055

NeuroControl of Nicotine Dependence

Led by University of Missouri-Columbia · Updated on 2024-10-01

30

Participants Needed

1

Research Sites

291 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

NeuroControl of Nicotine Dependence

Who Can Participate

Age: 18Years - 60Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Nicotine dependence defined by smoking at least 8 cigarettes per day for 2 or more years, with expired carbon monoxide levels of 10 ppm or higher, positive urine cotinine test, and FTND score of 3 or more; or using electronic cigarettes 15 or more times per day for at least 1 year with positive urine cotinine test and PS-ECDI score of 3 or more
  • Fluent in English
  • Functional vision (corrective lenses allowed)
Not Eligible

You will not qualify if you...

  • Use of psychotropic or antiepileptic medications within the last month
  • Presence of untreated illness or serious medical condition
  • History of major neurological illness
  • Contraindications to TMS or MRI, including history of neurological disorders, seizures, increased intracranial pressure, brain surgery, head trauma with loss of consciousness longer than 15 minutes, implanted electronic devices, or metal in the head
  • Use of substances that lower seizure threshold
  • Current or past psychosis
  • Electroconvulsive therapy within the past 6 months
  • Unstable cardiac disease, hypertension, severe kidney or liver insufficiency, or sleep apnea
  • Blood alcohol concentration greater than 0.0
  • Positive urine pregnancy test
  • Any other condition that could affect participant safety, study compliance, or result interpretation as judged by the investigator

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Health Neuroscience Center

Columbia, Missouri, United States, 65203

Actively Recruiting

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Research Team

B

Brett Froeliger, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

3

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