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No smoking be free: neuromodulation techniques for the treatment of nicotine addiction

No smoking be free: neuromodulation techniques for the treatment of nicotine addiction

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00037442
Enrollment
72
Registered
2025-07-17
Start date
2025-03-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

F17

Interventions

Group 1: Patients who underwent a combined method (tDCS+TMS) for the treatment of nicotine dependence, who underwent a 5-day treatment. The specific protocols for each method are given below: - TDCS p

Sponsors

University of Messina
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Ability to read and sign informed consent. Addiction and desire to smoke cigarettes. Subjects accessing the neuromodulation outpatient service.

Exclusion criteria

Exclusion criteria: Severe, unstable and concomitant active neurological or physical illnesses. Patients with schizophrenia. Patients with intellectual disability. Patients with substance-related disorders (other than tobacco/nicotine). Patients with previous episodes of epilepsy or unexplained seizures. Patients with implanted electronic devices and/or cochlear implants and/or vagus nerve stimulators. Patients with cardiac pacemakers. Patients with non-removable metal objects in proximity to the coil.

Design outcomes

Primary

MeasureTime frame
The primary outcome is evaluate whether the combined treatment was more effective than the single treatment. The textological evaluation will make it possible to observe these differences. Patients had received psychodiagnostic evaluation before treatment, at the end of treatment (5 days for the first arm and 21 for the second) and after six months of follow-up. Evaluation of nicotine dependence and nicotine withdrawal was assessed by the following psychometric instruments: - The Fagerström test, FTND (1991)consists of 6 questions, the scores obtained allow the classification of addiction to nicotine into five levels: very low (0 to 2 points); low (3 to 4 points); moderate (5 points); high (6 to 7 points); and very high (8 to 10 points). - The Smoking Abstinence Expectancies Questionnaire (SAEQ) is a rapid and reliable test that assesses the consequences of nicotine withdrawal in the short term. It is composed of 28 items and 4 subscales concerning: Negative mood, somatic symptoms, harmful consequences, and positive consequences. - Addictive Behavior Questionnaire (ABQ) is a self-report measure for the assessment of the different forms of addiction in all phases of the intervention.

Secondary

MeasureTime frame
Evaluate whether the combined treatment is longer lasting and better tolerated by the patients.

Countries

Italy

Contacts

Public ContactFiammetta Iannuzzo

University of Messina

fiannuzzo@unime.it+39 090 2212223

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 10, 2026