Substudy of Efficacy, Safety and Toxicology of Electronic Nicotine Delivery Systems as an Aid for Smoking Cessation (ESTxENDS Trial)- the Olfactory Function Substudy of ESTxENDS
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- University of Bern
- Enrollment
- 389
- Locations
- 5
- Primary Endpoint
- Assessment of olfactory function- Baseline
Study Overview
Brief Summary
--> This is a substudy of the main ESTxENDS trial (NCT03589989). Olfactory function outcomes should be considered secondary outcomes of the main smoking cessation outcome formulated in NCT03589989.
Up to one in five people have suffered loss or impairment of their sense of smell, limiting their available information about the environment, including possible hazards (e.g. gas or smoke). An impaired sense of smell is strongly associated with smoking, but its prevalence in smokers has yet to be established. Since only a few prospective cohort studies among smokers have compared change in olfactory function in smokers, it is not known how much or how fast smoking may impair olfactory function. Some studies describe improvement in olfactory function among quitters, supporting anecdotal evidence from ex-smokers who say they regained their sense of smell over time. As far as the investigators know, no randomized controlled trial has tested the effects of a smoking cessation intervention on olfactory function.
A reliable and validated olfactory function test is the Burghart Sniffin' Sticks 16-item Identification-test, which is quick and easy to administer. 16 familiar odours will be presented to the participants, each for 3-4 seconds. After each odour the participant is asked to select the correct answer from 4 possible answers.
With increasing popularity of e-cigarettes, their effect on the olfactory function also needs to be assessed. It is known, that e-cigarettes produce toxic compounds such as carbonyl and aldehydes, what could impair the sense of smell - especially if the liquid-level is too low or the temperature on the coil is too hot. This is the source of a phenomenon called "dry-hit", which is said to leave a burnt taste or smell to be recognized by users. However, it is unclear if e-cigarettes users with an olfactory dysfunction can adequately recognize a "dry-hit". Therefore, the goal is to investigate the effects of smoking cessation and use of ENDS on olfactory function and the recognition of a "dry-hit" from a test e-cigarette.
For the main ESTxENDS trial (NCT03589989), cigarette smokers motivated to quit smoking cigarettes will be included. Participants in the intervention group will receive an ENDS and nicotine-containing e-liquids, which they will be allowed to use ad libitum. Additionally, they will receive smoking cessation counseling. Participants in the control group will receive smoking cessation counseling only. All participants will be followed over a 24-month period. The primary objective is to assess changes in olfactory function from baseline to 6 months post target quit date (TQD) in cigarette smokers randomized to the intervention group compared to the control group.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Prevention
- Masking
- None
Masking Description
Statisticians and laboratory personnel will be blinded to group allocation
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Informed Consent as documented by signature
- •Persons aged 18 or older
- •Currently smoking 5 or more cigarettes a day for at least 12 months
- •Willing to try to quit smoking within the next 3 months,
- •Persons providing a valid phone number, a valid email address and/or a valid postal address.
Exclusion Criteria
- •Known hypersensitivity or allergy to contents of the e-liquid
- •Participation in another study with investigational drug within the 30 days preceding the baseline visit and during the present study where interactions are to be expected
- •Women who are pregnant or breast feeding
- •Intention to become pregnant during the course of the scheduled study intervention, i.e. within the first 6-months of the study
- •Persons having used ENDS or tobacco heating systems regularly in the 3 months preceding the baseline visit
- •Persons having used nicotine replacement therapy (NRT) or other medications with demonstrated efficacy as an aid for smoking cessation such as varenicline or bupropion within the 3 months preceding the baseline visit
- •Persons who cannot attend the 6- month follow-up visit for any reason
- •Cannot understand instructions delivered in person or by phone, or otherwise unable to participate in study procedures
Arms & Interventions
Intervention group
Intervention: ENDS (vaporizer/e-cig) and smoking cessation counseling (Other)
Control group
Intervention: Smoking cessation counseling (Other)
Outcomes
Primary Outcomes
Assessment of olfactory function- Baseline
Time Frame: Baseline
Assessment of olfactory function with the Burghart Sniffin' Sticks 16-item Identification-test. The highest possible score is 16; the cut-off for hyposmia is 11 and cut-off for anosmia is 8.
Assessment of olfactory function- follow-up
Time Frame: 6 months post quit date]
Assessment of olfactory function with the Burghart Sniffin' Sticks 16-item Identification-test. The highest possible score is 16; the cut-off for hyposmia is 11 and cut-off for anosmia is 8.
Secondary Outcomes
- Assessment of dry-hit recognition(6 months post quit date)
- Assessment of change of olfactory function(change from baseline to 6 months post quit date)