Lung cancer screening gets a Heart-Smart upgrade for heavy smokers
NCT ID NCT07301489
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether adding a heart disease prevention program to standard lung cancer screening can improve the health of heavy smokers. Researchers will use chest CT scans already taken for lung cancer screening to also check for hidden heart disease. 1000 participants will be followed for one year to see if this combined approach helps them reach goals like lower blood pressure, better cholesterol, and quitting smoking.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 1,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2025
- Expected to finish
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Apr 2041
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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60 to 79 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria used for the lung cancer screening implementation study/ TIDL Study: * Women and men * Ages 60 to 79 years old (inclusive) * A smoking history of at least 35 pack-years and 1) being a current smoker or a former smoker who quit less than 10 years prior or 2) having a PLCOm2012 model 6-year risk for lung cancer incidence over 2.6%. * Willingness and ability to comply with scheduled visits, laboratory tests, and other trial procedures * Written informed consent obtained prior to performing any protocol-related procedures * The participant should be affiliated to a social security system Exclusion Criteria used for the lung cancer screening implementation study/ TIDL Study: * Recent abnormal pulmonary findings under work-up of standard care * Having had chest CT \<1 year before potential entry into the study * Current or prior history of lung cancer, renal cancer, melanoma or breast cancer * Inability to provide signed informed consent * Insufficient understanding of the languages in which trial information is available * Psychiatric or other disorders that are incompatible with compliance to the protocol requirements and follow-up * Unable to be followed-up for at least 5-years * Body weight \>140 Kg because of difficulty of conducting the CT exam Inclusion Criteria used for the ACE 5 Study: * Participants from the TIDL Study with non-contrast, non-cardiac chest CT images available as part of the implementation lung cancer screening study * Signed consent for cardiovascular add on-study and agree to protocol, including follow-up visit 1-year after the baseline examination Exclusion Criteria used for the ACE 5 Study: * Any surgical or medical condition, including short life-expectancy, based on medical records or clinical findings prior to randomization, that will impair the ability of the patient to participate in the study * Patients unwilling or unable to comply with the protocol * History of non-compliance to medical management and patients who are considered potentially unreliable, based on information obtained prior to randomization * History or evidence of alcohol or drug abuse with the last 12 months, based on information obtained prior to randomization, that will influence study participation
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Akershus University Hospital
RECRUITINGLørenskog, Akershus, 1478, Norway
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