ClinicalTrials.gg
Not yet recruitingNCT07900724Updated Oct 28, 2026

New Smoking Cessation Intervention in Primary Care - a Randomized Controlled Trial

An interventional study of WillQuit App and Smoking cessation standard treatment, in Smoking Cessation and Smoking Cessation Counselling, sponsored by Helse Nord-Trøndelag HF. Not yet recruiting at 1 site in Norway. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-28.

Sponsored by Helse Nord-Trøndelag HF · Not applicable, Interventional, and Treatment

Updated Oct 28, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
620
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Cigarette smoking remains the leading modifiable risk factor for lung cancer4 and 16 other types of cancer, as well as chronic cardiovascular and pulmonary diseases. Despite public health efforts, smoking prevalence remains a major national as well as international challenge. Currently in Norway 16% of those 25-74 years of age are still daily or occasional smokers (9% and 7%, respectively), projecting a 10% of smoking prevalence during the current decade. In Europe it was estimated to be more than 183 millions current and former smokers (42% of the population) in 2017. Thus, smoking is a central public health issue nationally and internationally.

Smoking cessation not only significantly reduces lung cancer risk and other smoking related diseases, but also improves life expectancy, making this intervention a critical component of primary cancer prevention. Despite a decline in smoking rates, approximately 10% of Norwegians still smoke, with non-daily smoking on the rise among young people (16-24 years), affecting 19% of men and 13% of women. This underscores the urgent need for more effective cessation strategies.

A number of smoking cessation treatments have been developed, but the majority of people relapse within the first year of cessation. Primary care faces significant barriers in delivering effective smoking cessation interventions.

On the clinician side, challenges include a lack of personalized treatment options, time constraints, and unclear guidelines. From the patient perspective, there is often a lack of motivation and a perception that treatments are not tailored to individual needs.

This project aims to evaluate the effectiveness of a newly developed, personalized smoking cessation app designed to assists GPs in providing tailored smoking cessation treatments. Specifically, we will test whether the use of this app results in improved smoking cessation outcomes and enhanced quality of life for smokers in primary healthcare settings, compared to the current standard smoking cessation treatments.

Based on the results from the app, GPs will receive advice on how to motivate this particular person to quit smoking. The point of the app is that healthcare professionals will be able to provide a more personalized smoking cessation treatment based on the information that the smoker has entered into the app compared to current practice. Our hypothesis is that by using our newly developed app, healthcare professionals will be able to achieve better smoking cessation results compared to the standard smoking cessation approach used today.

The project is a clinical randomized-controlled phase 3 study in which we, through GP offices across the country, will include smokers who want to quit smoking to test this app. The intervention group (n=310) will be a group of smokers where the GP uses the app to help them quit smoking, while the control group (n=310) will be smokers who only receive regular smoking cessation treatment as is currently provided by GPs.

The health benefits of increased smoking cessation success rates are major, including prevention of various cancers as well as other chronic smoking-related diseases such as cardiovascular disease and lung disease e.g. COPD. This will in turn provide significant cost savings at a societal level.

02

Conditions studied

  • Smoking Cessation
  • Smoking Cessation Counselling

Browse trials for

Keywords

  • E-Lung Study
  • Primary prevention of lung cancer
  • Smoking cessation
  • Personalized smoking cessation
03

In context

Smoking Cessation

1,581 studies on the registry are indexed under Smoking Cessation; 198 are open to participants now.

This study's planned enrollment of 620 is above the median of 164 across 1,423 interventional studies indexed under Smoking Cessation.

Browse Smoking Cessation studies →

Lead sponsor

Helse Nord-Trøndelag HF is the lead sponsor of 27 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria: ≥ 18 years of age, current smoker (either daily or occasionally), interested to discuss smoke cessation, competent of consent.

-

Exclusion Criteria: Non-smokers, \<18 years of age.

-

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Investigator)
Enrollment
620 participants (estimated)

Study arms

  • Active comparator
    Control group

    Receiving standard smoking cessation treatment

    Behavioral: Smoking cessation standard treatment,

  • Experimental
    Intervention group

    Receving personalized smoking cessation treatment based on a newly developed App

    Behavioral: WillQuit App

Interventions

  • BehavioralWillQuit App

    WillQuit App is a newly developed, personalized smoking cessation app designed to assists GPs in providing tailored smoking cessation treatments.

  • BehavioralSmoking cessation standard treatment,

    Smoking cessation by using standard treatment.

06

What researchers measure

Primary outcomes

  1. Rate of smoking cessation

    Rate of smoking cessation between the intervention and the control

    Time frame: From enrollment to 1 year after.

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Yes

Supporting information: Study protocol, Informed consent form, Clinical study report

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 28, 2026
Show all 1 update
  1. Oct 28, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07900724
Lead sponsor
Helse Nord-Trøndelag HF
Responsible party
Sponsor
First posted
Oct 28, 2026
Start date
Jan 2027 (estimated)
Primary completion
Jan 2029 (estimated)
Completion
Dec 2029 (estimated)
Last update
Oct 28, 2026

Study contacts

Oluf Dimitri Roe, Professor, MD
Contact
oluf.roe@ntnu.no
+47 95432496
Olav Toai Duc Nguyen, MD, PhD
Contact
olavtoaiduc.nguyen@helse-nordtrondelag.no
+47 48228841

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion