Actively Recruiting
Integrating Smoking Cessation With Low-dose CT-screening for Lung Cancer
Led by Oulu University Hospital · Updated on 2026-02-06
1200
Participants Needed
5
Research Sites
551 weeks
Total Duration
On this page
Sponsors
O
Oulu University Hospital
Lead Sponsor
F
Finnish Cancer Society
Collaborating Sponsor
AI-Summary
What this Trial Is About
The study investigates effectiveness of different smoking cessation methods and low-dose CT based lung cancer screening
CONDITIONS
Official Title
Integrating Smoking Cessation With Low-dose CT-screening for Lung Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Able to provide written informed consent
- Age between 50 and 74 years
- Smoked 6 15 cigarettes per day for 6 25 years or smoked 6 10 cigarettes per day for 6 30 years and are active smokers (smoking during the last two weeks)
- Access to a smartphone (iPhone or Android)
You will not qualify if you...
- Current or past melanoma, lung, renal or breast cancer
- A chest CT examination less than one year before inclusion
- Known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial
- No access to a smartphone (iPhone or Android)
- Participant is unwilling or unable to comply with treatment and trial instructions
- Any condition that study investigators consider an impediment to safe trial participation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 5 locations
1
Helsinki University Hospital
Helsinki, Finland
Not Yet Recruiting
2
Oulu University Hospital
Oulu, Finland
Actively Recruiting
3
Tampere University Hospital
Tampere, Finland
Not Yet Recruiting
4
Turku University Hospital
Turku, Finland
Not Yet Recruiting
5
Vaasa Central Hospital
Vaasa, Finland
Not Yet Recruiting
Research Team
J
Jussi P Koivunen, MD, PhD
CONTACT
S
Sanna Iivanainen, MD, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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