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Reduce Tobacco Use in People Living With HIV in Switzerland

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06789692
Acronym
RETUNE
Enrollment
972
Registered
2025-01-23
Start date
2025-02-20
Completion date
2027-12-01
Last updated
2026-06-02

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

Conditions

HIV, Smoking

Keywords

tobacco smoking, e-cigarettes, tobacco-free nicotine pouches, Trials within Cohorts (TwiCs)

Brief summary

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.

Detailed description

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.

Interventions

OTHERtobacco 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.

Sponsors

University Hospital, Basel, Switzerland
Lead SponsorOTHER
Swiss National Science Foundation
CollaboratorOTHER
Novartis Foundation for Medical-Biological Research
CollaboratorUNKNOWN

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Randomized Clinical Trial using the Trials within Cohorts (TwiCs) design

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Tobacco smoking status (yes/no)at 6 month visitMeasured as self-reported abstinence in the last 7 day at 6-month visit

Secondary

MeasureTime frameDescription
Tobacco smoking status (yes/no)at 12 month visit, 24-month visitMeasured as self-reported abstinence in the last 7 day at 12-month visit and at 24-month visit
Mean change in number of tobacco-based cigarettes smoked per dayat 6 month visit, at 12 month visit, at 24 month visitNumber will be self reported by participant
Mean Change in Cholesterol (mmol/l)at 6 month visit, at 12 month visit, at 24 month visitHigh Density Lipoprotein (HDL) and Low Density Lipoprotein (LDL) Cholesterol in blood samples will be measured
Mean change in blood pressure (mmHg)at 6 month visit, at 12 month visit, at 24 month visitsystolic and diastolic blood pressure will be measured.
Mean change in body weight (kg)at 6 month visit, at 12 month visit, at 24 month visitMean change in body weight from baseline to 6,12 and 24 months.
Mean change in SCORE2-risk prediction algorithmat 6 month visit, at 12 month visit, at 24 month visitSCORE2: 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.
Number of cardiovascular eventsat 6 month visit, at 12 month visit, at 24 month visitOccurrence 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
Serious Adverse eventsat 6 month visit, at 12 month visit, at 24 month visitThis endpoint will be presented descriptively.
Self reported use of any nicotine containing product other than tobacco cigarettes (yes/no)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)at 6 month visit, at 12 month visit, at 24 month visit
Self reported use of any nicotine containing product (yes/no)at 6 month visit, at 12 month visit, at 24 month visit

Countries

Switzerland

Contacts

CONTACTMatthias Briel, Prof.
matthias.briel@usb.ch+ 4161 265 3815
CONTACTChristof Schönenberger, Dr.
ChristofManuel.Schoenenberger@usb.ch
PRINCIPAL_INVESTIGATORMatthias Briel, Prof.

University Hospital, Basel, Switzerland

PRINCIPAL_INVESTIGATORAlain Amstutz, Dr.

University Hospital, Basel, Switzerland

PRINCIPAL_INVESTIGATORChristof Schönenberger, Dr.

University Hospital, Basel, Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 3, 2026