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Идёт набор NCT06789692

Reduce Tobacco Use in People Living With HIV in Switzerland

Без фазы С лечением HIV Smoking

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: tobacco smoking substitution products.
Кому может быть актуально
Состояния в реестре: HIV, Smoking. 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
Швейцария
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Reduce Tobacco Use in People Living With HIV in Switzerland: A Pragmatic Randomized Trial Within the Swiss HIV Cohort Study

Обзор

The purpose of this trial is to test the effectiveness of offering a menu of different tobacco smoking substitutional products (e-cigarettes, nicotine pouches, nicotine patches in addition to usual of care) for smokers in the SHCS (Swiss HIV Cohort Study) in achieving self-reported 7-day tobacco cigarette abstinence at 6 months.

Подробное описание

Due to highly effective antiretroviral therapy, people living with HIV (PLWH) in Switzerland have a close-to-normal life expectancy. Among PLWH, there has been a shift of focus from HIV-related health issues to non communicable diseases, especially cardiovascular diseases (CVDs) and cancer. Smoking, a prominent risk factor for both diseases, takes a key role in view of the high number of smokers among PLWH.

New approaches to smoking cessation focus on harm reduction by substituting tobacco cigarettes by less harmful alternatives. Conventional nicotine replacement therapy like nicotine patches is well established and effective against withdrawal symptoms after quitting. However, these products are exceptionally expensive and the missing "nicotine hit" often limits therapy adherence. The long-term abstinence rate remains low. Electronic cigarettes (e-cigarettes) and nicotine pouches as alternative nicotine replacement therapies have the potential to overcome these problems and are accessible.

E-cigarettes play a growing role in smoking cessation therapy. Evidence from randomized trials shows superiority over conventional nicotine replacement therapies, which is probably based on the better imitation of the smoking experience. Although e-cigarettes are not without concerns, there is consensus that they are significantly less harmful than tobacco cigarettes.

Tobacco-free nicotine pouches, delivering nicotine through oral mucosa, are a relatively novel option for nicotine substitution. Similar to e-cigarettes, nicotine pouches are relatively affordable and can address the limitation of poor imitation of the "nicotine hit" seen with traditional nicotine replacement therapy. To the best of our knowledge, no trials have investigated the potential of nicotine pouches for smoking cessation so far.

With this trial, the investigators also want to address frequent shortcomings of smoking cessation trials, such as restrictive inclusion criteria and highly controlled interventions, by RETUNE Version 1.1, January 06, 2025 10/45 offering a menu of different tobacco smoking substitutional products (e-cigarettes or nicotine pouches or nicotine patches) and by using a novel pragmatic trial design, the Trials within Cohorts (TwiCs) design. The investigators plan to recruit tobacco smokers in the Swiss HIV Cohort Study (SHCS), regardless of their willingness to quit. This so called "opt-out-approach" has been suggested as a new promising approach for smoking cessation trials to increase generalizability of the results. The TwiCs design optimally allows to implement and evaluate the "opt-out" approach embedded in the SHCS.

Вмешательства

  • Другое tobacco smoking substitution products
    Offer of preference-based smoking substitution menu, consisting of e-cigarettes or nicotine pouches or nicotine patches in addition to standard of care. This menu will be offered by the treating physician during the routine cohort visit and the participant can choose one product to test as an alternative to tobacco smoking. The products will be handed out directly after the consultation and are provided free of charge for 6 months.

Первичные конечные точки

  • Tobacco smoking status (yes/no) [Срок оценки: at 6 month visit]
Вторичные конечные точки (11)
  • Tobacco smoking status (yes/no) [Срок оценки: at 12 month visit, 24-month visit]
  • Mean change in number of tobacco-based cigarettes smoked per day [Срок оценки: at 6 month visit, at 12 month visit, at 24 month visit]
  • Mean Change in Cholesterol (mmol/l) [Срок оценки: at 6 month visit, at 12 month visit, at 24 month visit]
  • Mean change in blood pressure (mmHg) [Срок оценки: at 6 month visit, at 12 month visit, at 24 month visit]
  • Mean change in body weight (kg) [Срок оценки: at 6 month visit, at 12 month visit, at 24 month visit]
  • Mean change in SCORE2-risk prediction algorithm [Срок оценки: at 6 month visit, at 12 month visit, at 24 month visit]
  • Number of cardiovascular events [Срок оценки: at 6 month visit, at 12 month visit, at 24 month visit]
  • Serious Adverse events [Срок оценки: at 6 month visit, at 12 month visit, at 24 month visit]
  • Self reported use of any nicotine containing product other than tobacco cigarettes (yes/no) [Срок оценки: at 6 month visit, at 12 month visit, at 24 month visit]
  • Self reported use of e-cigarettes (yes/no) or nicotine pouches (yes/no) or nicotine patches (yes/no) [Срок оценки: at 6 month visit, at 12 month visit, at 24 month visit]
  • Self reported use of any nicotine containing product (yes/no) [Срок оценки: at 6 month visit, at 12 month visit, at 24 month visit]

Критерии участия

Критерии включения

  • Signed informed consent for the data collection and participation in the SHCS (Cohort consent).
  • Signed informed consent to be randomized to future interventions (Randomization consent).
  • Age 18 years or older.
  • Smoked one or more tobacco cigarettes per day (smoking status = yes) at the time of enrolment.

Критерии исключения

  • Currently using e-cigarettes or nicotine pouches or nicotine patches.
  • Pregnant women.

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Профилактика

Центры проведения

Швейцария · 7 центров
  • University Hospital Basel — Basel
  • Inselspital Bern — Bern
  • Cantonal Hospital St. Gallen — Sankt Gallen
  • University Hospital Lausanne — Lausanne
  • University Hospital Zurich — Zurich
  • Cantonal Hospital Aarau — Aarau
  • University Hospital Geneva — Geneva

Публикации

  • Schonenberger CM, Ochoa SC, Speich B, Haerry DH, Cart-Richter E, Jackson-Perry D, Hutter A, Panettieri L, Aggeler S, Chaudron SE, Calmy A, Cavassini M, Abela IA, Kusejko K, Gunthard HF, Nemeth J, Rauch A, Wandeler G, Schmid P, Dorr T, Surial B, Berthet A, Auer R, Stoeckle MP, Labhardt N, Chammartin F, Briel M, Amstutz A. Acceptance and preferences for different nicotine substitute products to redu PMID 42205972
  • Schonenberger CM, Speich B, Zehnder ER, Haerry DH, Cart-Richter E, Jackson-Perry D, Hutter A, Aggeler S, Steinmann J, Chaudron SE, Calmy A, Cavassini M, Braun D, Fux CA, Abela I, Kusejko K, Gunthard HF, Nemeth J, Rauch A, Wandeler G, Schmid P, Dorr T, Notter J, Weisser Rohacek M, Surial B, Berthet A, Auer R, Stoeckle MP, Labhardt N, Chammartin F, Briel M, Amstutz A; Swiss HIV Cohort Study. Offer o PMID 41952225

Идентификаторы

NCT: NCT06789692 · 2024-02417; ub25Briel

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗