Smoking
Conditions
Interventions
Participants are 1:1 randomized into intervention or control group using permuted blocks randomization. Each trial participant will take part in group-based training sessions aimed at smoking cessatio
Sponsors
Erasmus MC
Eligibility
Inclusion criteria
Inclusion criteria: In order to be eligible for participation in the trial, a participant must meet the following criteria: (1) aged 18 years or over, (2) employed at one of the participating health care institutions, and (3) a daily smoker (i.e. smoking at least one cigarette per day)
Exclusion criteria
Exclusion criteria: A person who meets any of the following criteria will not be eligible for participation in this study: (1) only using e-cigarettes and (2) not being able to physically attend the group-based training sessions.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Biochemically validated smoking cessation at t = 12 | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary end-points are self-reported biochemically validated smoking cessation at t=0, t=3, t=6 and t=15. Tertiary outcomes are the incremental cost-effectiveness ratio and the incremental cost utility ratio, where the first is calculated using the total costs per quitter and the latter by the costs and self-reported quality of life (EQ-5D). | — |
Contacts
Public ContactNienke Boderie
Erasmus MC
Outcome results
None listed