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Идёт набор NCT04209153

Direct Transcranial Electrical Stimulation in Tobacco Addiction (tDCS)

Наблюдательное Adults (Male and Female Subjects) With Tobacco Dependence

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Transcranial Direct Current Stimulation.
Кому может быть актуально
Состояния в реестре: Adults (Male and Female Subjects) With Tobacco Dependence. Базовые параметры: от 18 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Франция
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Evaluation of the Effect of Transcranial Direct Current Stimulation (tDCS) in Nicotine-Dependent Tobacco Users

Обзор

In summary, there are currently many therapeutic tools for achieving some degree of control or even cessation of tobacco addictive use. No single therapy seems to have proven itself sufficiently effective to be the preferred treatment axis in the management of this addiction. We can also point out that so far the main treatments aimed at reducing or controlling the craving phenomenon are of a pharmacological nature, thus exposing the participants to the side effects inherent to this type of treatment. In this perspective, the establishment of non invasive brain stimulation (TdCS), acting in a targeted manner on craving and whose effects would be mild and transient, appears quite justified, especially in addition to psychotherapy. In the context of the management of addictive pathologies, the choice of smoking dependence seems relevant to us insofar as this addiction represents a major public health problem.

Вмешательства

  • Другое Transcranial Direct Current Stimulation
    tDCS sessions (with Direct Transcranial Electrical Stimulation (tDCS) device - Neuroelectrics

Первичные конечные точки

  • Fagerström score (3 is the highest score and O the lowest one for item 1. A score of 1 or 2 means low dependence (for item 1 only as well as if you use the total score) [Срок оценки: 15 days]
Вторичные конечные точки (1)
  • tobacco consumption [Срок оценки: 15 days]

Критерии участия

Критерии включения

  • Men and women over the age of 18
  • Nicotine dependent subjects according to the Fagerström test (score ≥5)
  • Subjects consuming daily tobacco.
  • Subjects understanding and reading French and able to express themselves in this language.
  • Signed informed consent to participate indicating that the subject has understood the purpose and the procedures required by the study and agrees to participate in the study and to comply with the requirements and limitations of this study
  • Affiliation to the French social security scheme or beneficiary of such a scheme.
  • No other method to decrease or stop smoking at the same time as the study.

Критерии исключения

  • Guardianship
  • Pregnant or lactating woman
  • Patient under AME
  • Subject being in the exclusion period of another study or provided for by the "National Volunteer File".
  • Subjects with intracranial hypertension
  • Subject unlikely to cooperate with the study and / or weak cooperation anticipated by the investigator.
  • Treatment with buproprion or varenicline in progress
  • Episode or family history of epilepsy, convulsion.
  • Disease causing damage to the brain (aneurysm, tumor, ...).
  • Cochlear or ocular implant.
  • Stimulator or cardiac defibrillator.
  • Presence of metal in the skull (clip on aneurysm, prosthesis, ...).
  • Eczema on the scalp.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Дизайн исследования

Модель наблюдения
Когортное

Центры проведения

Франция · 1 центр
  • Psychiatrie Adultes Et Addictologie — Paris

Идентификаторы

NCT: NCT04209153 · APHP190731 · 2019-A01946-51

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗