Smoking CessationNCT07900724
New Smoking Cessation Intervention in Primary Care - a Randomized Controlled Trial
A study testing WillQuit App and Smoking cessation standard treatment, in people with Smoking Cessation and Smoking Cessation Counselling, run by Helse Nord-Trøndelag HF at 1 site in Norway.
Trial 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. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Smoking Cessation, Smoking Cessation Counselling
- What is being tested?
- WillQuit App and Smoking cessation standard treatment,
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 620 participants
- Where
- 1 siteNorway
- Study dates
- Jan 2027to Dec 2029
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
None listed.
Who cannot join
- -
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Norway1 site
Levanger Hospital
Levanger, Trøndelag, 7601
Oluf Dimitri Roe, Professor, MD, +47 95432496, oluf.roe@ntnu.no
Olav Toai Duc Nguyen, MD, PHD, +47 48228841, olavtoaiduc.nguyen@helse-nordtrondelag.no
About this study
Official title: Primary Prevention of Lung Cancer With a New Tool for Smoke Cessation in General Practice in Norway: The E-Lung Study.
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.
Read more
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.
- Conditions
- Smoking Cessation, Smoking Cessation Counselling
- Being tested
- WillQuit App, Smoking cessation standard treatment,
- Keywords
- E-Lung Study, Primary prevention of lung cancer, Smoking cessation, Personalized smoking cessation
- Medical subject headings
- Smoking Cessation
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
WillQuit AppBehavioural
WillQuit App is a newly developed, personalized smoking cessation app designed to assists GPs in providing tailored smoking cessation treatments.
Smoking cessation standard treatment,Behavioural
Smoking cessation by using standard treatment.
| Study group | Role | What they receive |
|---|---|---|
| Control group | Active comparator | Receiving standard smoking cessation treatment Receives: Behavioral: Smoking cessation standard treatment, |
| Intervention group | Experimental | Receving personalized smoking cessation treatment based on a newly developed App Receives: Behavioral: WillQuit App |
What is being measured
The primary outcome is the main question the study is designed to answer.
Rate of smoking cessation
Rate of smoking cessation between the intervention and the control
Measured: From enrollment to 1 year after.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Oct 2026
- Study startJan 2027 (estimated)
- Primary completionJan 2029 (estimated)
- Study completionDec 2029 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Smoking CessationStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Randomized control clinical trial.
- Masking
- Single blind
- Who is masked
- Investigator
- Enrolment
- 620 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Helse Nord-Trøndelag HF
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07900724
- Sponsor's protocol ID
- 668599
- Status last verified
- Oct 2026
- First submitted
- 21 Oct 2026
- Last updated
- 28 Oct 2026
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 28 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Primary Prevention of Lung Cancer With a New Tool for Smoke Cessation in General Practice in Norway: The E-Lung Study.
- ClinicalTrials.gov ID
- NCT07900724
- Acronym / sponsor ID
- 668599
- Conditions
- Smoking Cessation, Smoking Cessation Counselling
- Keywords
- E-Lung Study, Primary prevention of lung cancer, Smoking cessation, Personalized smoking cessation
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 620 participants (estimated)
- Lead sponsor
- Helse Nord-Trøndelag HFUniversity, hospital or other
- Study start
- Jan 2027 (estimated)
- Primary completion
- Jan 2029 (estimated)
- Study completion
- Dec 2029 (estimated)
- First posted
- 28 Oct 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (investigator)
- Number of arms
- 2
- Model description
- Randomized control clinical trial.
| Arm | Type | Receives |
|---|---|---|
| Control group | Active comparator | Behavioral: Smoking cessation standard treatment,Receiving standard smoking cessation treatment |
| Intervention group | Experimental | Behavioral: WillQuit AppReceving personalized smoking cessation treatment based on a newly developed App |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (0 listed)
Key exclusion criteria (1 listed)
- -
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| WillQuit AppWillQuit App is a newly developed, personalized smoking cessation app designed to assists GPs in providing tailored smoking cessation treatments. | Behavioural | Intervention group |
| Smoking cessation standard treatment,Smoking cessation by using standard treatment. | Behavioural | Control group |
Primary outcome
Rate of smoking cessation
Time frame: From enrollment to 1 year after.
Rate of smoking cessation between the intervention and the control
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Oct 2026.
- Individual participant dataSharing planned: Yes
Related trials for Smoking Cessation
Active, not recruiting
An Interactive Smartphone Application to Motivate Smokers to Quit
Smoking Cessation, Smoking Behaviors
Not yet recruiting
Comparing the Efficacy of a Conversational Agent (QuitBot) Versus Standard Health Education on Smoking Cessation Among Medical Students; A Randomized Controlled Trial.
Conversational Agent, Smoking Cessation
Enrolling by invitationObservational study
Using Smartwatches to Monitor Smoking in Real-life Situations
Smoking
Active, not recruitingPhase 3
Early Withdrawal Exposure and Negative Affect Withdrawal (NAW) Regulation Training for Smoking Cessation
Tobacco Dependence
Active, not recruitingEarly Phase 1
Smoking Cessation Intervention During Low Dose CT (LDCT) Screening for Lung Cancer
Smoking Cessation
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing WillQuit App and Smoking cessation standard treatment, in people with Smoking Cessation and Smoking Cessation Counselling, run by Helse Nord-Trøndelag HF at 1 site in Norway.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 0 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 28 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Norway. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Oluf Dimitri Roe, Professor, MD (+47 95432496, oluf.roe@ntnu.no), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Rate of smoking cessation (time frame: From enrollment to 1 year after.). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Oct 2026.