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NCT Number: NCT06789692

Reduce Tobacco Use in People Living With HIV in Switzerland

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital Basel, Basel, Switzerland

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

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

Treatment and study plan

tobacco smoking substitution products

Other

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.

Primary outcomes

  1. Tobacco smoking status (yes/no)

    Time frame: at 6 month visit

    Measured as self-reported abstinence in the last 7 day at 6-month visit

Secondary outcomes

  1. Tobacco smoking status (yes/no)

    Time frame: at 12 month visit, 24-month visit

    Measured as self-reported abstinence in the last 7 day at 12-month visit and at 24-month visit

  2. Mean change in number of tobacco-based cigarettes smoked per day

    Time frame: at 6 month visit, at 12 month visit, at 24 month visit

    Number will be self reported by participant

  3. Mean Change in Cholesterol (mmol/l)

    Time frame: at 6 month visit, at 12 month visit, at 24 month visit

    High Density Lipoprotein (HDL) and Low Density Lipoprotein (LDL) Cholesterol in blood samples will be measured

  4. Mean change in blood pressure (mmHg)

    Time frame: at 6 month visit, at 12 month visit, at 24 month visit

    systolic and diastolic blood pressure will be measured.

  5. Mean change in body weight (kg)

    Time frame: at 6 month visit, at 12 month visit, at 24 month visit

    Mean change in body weight from baseline to 6,12 and 24 months.

  6. Mean change in SCORE2-risk prediction algorithm

    Time frame: at 6 month visit, at 12 month visit, at 24 month visit

    SCORE2: Algorithm to Predict Cardiovascular Disease Risk in Europe Linear regression model adjusted for the variables used in the minimization (region [French vs. German speaking part of Switzerland], men having sex with men [yes/no], current drug user [yes/no], number of cigarettes per day) and will be reported as an adjusted odds ratio with 95% confidence interval.

  7. Number of cardiovascular events

    Time frame: at 6 month visit, at 12 month visit, at 24 month visit

    Occurrence of cardiovascular events (myocardial infarction, coronary angioplasty/stenting, coronary artery by-pass grafting, carotid endarterectomy, stroke, deep vein thrombosis, pulmonary embolism, heart transplantation) and all-cause death

  8. Serious Adverse events

    Time frame: at 6 month visit, at 12 month visit, at 24 month visit

    This endpoint will be presented descriptively.

  9. Self reported use of any nicotine containing product other than tobacco cigarettes (yes/no)

    Time frame: at 6 month visit, at 12 month visit, at 24 month visit

  10. Self reported use of e-cigarettes (yes/no) or nicotine pouches (yes/no) or nicotine patches (yes/no)

    Time frame: at 6 month visit, at 12 month visit, at 24 month visit

  11. Self reported use of any nicotine containing product (yes/no)

    Time frame: at 6 month visit, at 12 month visit, at 24 month visit

Study contacts

Contact information is provided by the study sponsor or research team.

Christof Schönenberger, Dr.

CONTACT

[email protected]

Matthias Briel, Prof.

CONTACT

[email protected]

+ 4161 265 3815

Sponsors and collaborators

Lead sponsor

University Hospital, Basel, Switzerland

Other

Collaborators

  • Novartis Foundation for Medical-Biological Research
  • Swiss National Science Foundation

Registry information

Official study title

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

Acronym: RETUNE

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Jan 23, 2025
Registry last updated
Jun 2, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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