Tobacco Dependence TreatmentICARE-LCSNCT06745258
ICARE-LCS QUERI Partnered Evaluation Initiative: Integrating Comprehensive Tobacco Treatment to Enhance Lung Cancer Screening
An observational study of Tobacco Dependence Treatment and Lung Cancer Screening, run by VA Office of Research and Development at 1 site in United States.
Trial summary
Lung cancer is the leading cause of cancer-related death among Veterans with 90% of cases attributable to smoking. Lung cancer screening (LCS) combined with smoking cessation saves the most lives. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Tobacco Dependence Treatment, Lung Cancer Screening
- What is being tested?
- External Facilitation
- How many people
- 7 participants
- Where
- 1 siteUnited States
- Study dates
- 1 Oct 2026to 30 Jun 2027
- Phase
- Observational
- 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 Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: Participating VA Medical Centers
Who may be able to join
- This is a VAMC based Quality Improvement Partnered Evaluation Initiative. VA sites from around the country that agreed to participate are included.
Who cannot join
- N/A
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
United States1 site
Minneapolis VA Health Care System, Minneapolis, MN
Minneapolis, Minnesota, 55417-2309
Anne C Melzer, MD MS, (612) 725-2000 ext. 4400, Anne.Melzer2@va.gov
Megan E Campbell, (612) 725-2000 ext. x7225, megan.campbell@va.gov
About this study
Official title: ICARE-LCS QUERI Partnered Evaluation Initiative: Integrating Comprehensive Tobacco Treatment to Enhance Lung Cancer Screening (PEC 24-239)
Lung cancer is the leading cause of cancer-related death among Veterans with 90% of cases attributable to smoking. Lung cancer screening (LCS) combined with smoking cessation saves the most lives. ICARE-LCS seeks to decrease health inequality and improve Veteran health by reducing smoking rates among Veterans receiving LCS. ICARE-LCS will use implementation methods to inform national cancer prevention efforts and build infrastructure necessary to support broad implementation of high-impact tobacco dependence treatment (TDT) processes in LCS programs.
Read the detailed description
The primary goal is to improve the delivery of tobacco dependence treatment (TDT) within Veterans Affairs (VA) lung cancer screening (LCS) programs. LCS with annual low-dose computed tomography saves lives through the early detection of lung cancer and is being broadly deployed, now at 113 VA medical centers. Due to the eligibility criteria selecting for current or previous smoking, 50-60% of LCS participants currently smoke. Modeling studies support that integrating TDT into LCS nearly doubles the benefit of the screening itself. Therefore, access to high-quality TDT is a program requirement per the VA LCS guidance memo.
Though a robust integration of LCS and TDT is a VA priority, in reality there remains a gap in both reach and intensity of TDT for LCS participants. Guidelines and evidence support TDT processes that include 1) systematic assessment and connection to treatment (e.g. Ask-Advise-Connect, motivational interviewing, optout or proactive strategies) and 2) treatment that includes the evidence-based combination of intensive pharmacologic and behavioral treatments ('combined TDT'). Recent trials in LCS participants found high rates of agreeing to treatment using 'opt-out' motivational referral strategies and the highest cessation rates using a longitudinal "chronic disease" model that delivers combined TDT over a period up to a year. Unfortunately, relatively few Veterans in LCS receive any TDT and the treatment is usually inconsistent with guidelines and this evidence. In a national sample of LCS participants who smoke, only 16.4% received any pharmacotherapy for TDT, many under-dosed with short-acting nicotine replacement alone, and fewer than 1% received the recommended combination of behavioral and pharmacologic treatment. This represents a significant gap in care. Improving quality of TDT for Veterans in LCS has been identified as a priority area by multiple stakeholders including the Office of Oncology and Precision Medicine (OPM), the investigators' operational partner, the VA Lung Precision Oncology Program (LPOP), the White House Prevention and Screening Task Force, the National Committee for Quality Assurance and Veterans engagement groups. Each care process-LCS and TDT-is complex on its own, which has hampered integration. While some LCS processes are standardized across VA through use of the tools provided by the National Center for Lung Cancer Screening (NCLCS), individual LCS programs use varied care models. Programs can be 'centralized' (most LCS-related care is delivered by dedicated program staff) or 'hybrid,' where responsibilities are shared between primary care and LCS staff. NCLCS has worked with VAs across the country to enhance LCS quality and uptake. Individual LCS programs deliver combined TDT variably, and many processes are not adapted for the longitudinal, annual LCS process. The VA Tobacco Use Treatment Program Office (TUT) is currently conducting a pilot funded by the Cancer Moonshot to demonstrate feasibility of integrating TDT into LCS, recently expanded from 11 to 15 sites. The Minneapolis VA has conducted a VISN 23-Quality Enhancement Research Initiative (QUERI) partnered implementation pilot to understand barriers and needs among diverse LCS programs, identifying many modifiable targets. The VISN 23 QUERI Team and TUT have collaborated to design an LCS-TDT toolkit that will soon be nationally available. While an important step, a toolkit alone may be insufficient to increase uptake of best practices. Tailored implementation support through intensive external facilitation may be necessary to effectively integrate TDT processes within the VA LCS landscape. With support from the operational partner, OPM, this project proposes to work with TUT and the NCLCS to build on existing efforts to increase participation in combined TDT for LCS participants. This project will utilize both retrospective data analysis and prospective data gathering to inform and tailor a toolkit for national dissemination. ICARE-LCS is an implementation evaluation study model.
Specific Aims:
Aim 1: Identify key process components of effective tobacco treatment programs in LCS and success factors for providing combined TDT. A mixed methods assessment will be conducted at 10 sites in the TUT Moonshot pilot, first qualitatively assessing their current TDT-LCS processes, success factors and perceived barriers to implementation of combined TDT. Data will then be linked with quantitative data of treatment participation and short-term cessation. Findings will be used to refine the toolkit for use in Aim 2 and nationally.
Aim 2: Test a multicomponent facilitation package to improve integration of TDT and LCS.
Seven programs will be identified from among LPOP sites outside of the TUT pilot, ensuring variation in site characteristics (e.g. hybrid vs centralized model), and provided implementation support using external facilitation. Sites will be matched at least 1:1 to another site in the LPOP network that will receive implementation as usual (controls). The primary outcome will be penetration (participation in combined TDT, secondary outcome any treatment) with additional secondary outcomes of fidelity (ideal TDT), and effectiveness (short-term cessation).
Aim 3: Evaluate the implementation outcomes of feasibility, acceptability, fidelity, appropriateness, and cost of implementing TDT integrated with LCS, assessed among Veterans and care team members.
Implementation outcomes other than cost will be assessed using qualitative methods. Cost will be examined related to the implementation support and to the TDT provided (e.g. LCS staff costs, pharmacotherapy, tobacco-related visits) using staff logs and VA pharmacy and billing data. Collectively, the above program evaluation will inform national cancer prevention efforts and build infrastructure necessary to support broad implementation of high-impact TDT processes in LCS programs.
- Being tested
- External Facilitation
- Keywords
- Lung Cancer, Lung Nodule, Tobacco, Lung Cancer Screening
- Medical subject headings
- Lung Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
External FacilitationOther
Multi-component facilitation strategy to address identified implementation needs
| Study group | Role | What they receive |
|---|---|---|
| Veterans Participating in Lung Cancer Screening who Smoke | Veterans participating in lung cancer screening who smoke and are receiving care at participating VA medical centers | |
| Participating VA Medical Centers | Seven sites that have agreed to participate in implementation intervention Receives: Other: External Facilitation |
What is being measured
The primary outcome is the main question the study is designed to answer.
Receipt of Combined Tobacco Dependence Treatment
Participation in counseling and pharmacotherapy within 90 days of lung cancer screening referral
Measured: Approximately 3 years
Secondary outcomes (5)
Number of Veterans Receiving ANY Tobacco Dependence Treatment Therapy
Participation in ANY tobacco dependence treatment therapy (including but not limited to pharmacotherapy or counseling) for eligible Veterans in lung cancer screening who smoke
Measured: Approximately 3 years
Number of Veterans Receiving of Pharmacotherapy or Counseling Alone
Participation in individual treatment options among patients in lung cancer screening who smoke. These are defined as Pharmacotherapy (nicotine replacement, bupropion, varenicline, combination treatments) and counseling (individual or group tobacco visits delivered by any modality).
Measured: Approximately 3 years
Cost Associated with Tobacco Dependence Treatment Among Lung Cancer Screening Participants who Smoke
Evaluate facility level costs and economic impacts of tobacco treatment for patients in lung cancer screening who smoke.
Measured: Approximately 3 years
Rate of Short-term Cessation Among Veterans In Lung Cancer Screening who Smoke
Short-term cessation data among eligible Veterans in lung cancer screening who smoke as gathered by chart review
Measured: Approximately 3 years
Implementation Outcomes Assessed at Participating Sites
Assessing implementation outcomes by qualitative review.
Measured: Approximately 3 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Dec 2024
- Study start1 Oct 2026 (estimated)
- Primary completion30 Jun 2027 (estimated)
- Study completion30 Jun 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Tobacco Dependence TreatmentStudies of the same condition, open and under way.
- More trials run by VA Office of Research and DevelopmentThe sponsor's other registered studies.
- 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
- Observational
- Observational model
- Other
- Time perspective
- Other
- Enrolment
- 7 participants (estimated)
Sponsor and investigators
- Lead sponsor
- VA Office of Research and Development
- Sponsor type
- US federal agency
- Collaborators
- VA Oncology and Precision Medicine, VA Tobacco Use Treatment National Program Office, VA National Center for Lung Cancer Screening
- Responsible party
- Sponsor
- Investigators
- Anne C. Melzer, MD MS, Principal investigator, Minneapolis VA Health Care System, Minneapolis, MN
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06745258
- Sponsor's protocol ID
- PEX 24-002
- Acronym
- ICARE-LCS
- Status last verified
- May 2026
- First submitted
- 16 Dec 2024
- Last updated
- 26 May 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 26 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- ICARE-LCS QUERI Partnered Evaluation Initiative: Integrating Comprehensive Tobacco Treatment to Enhance Lung Cancer Screening (PEC 24-239)
- ClinicalTrials.gov ID
- NCT06745258
- Acronym / sponsor ID
- ICARE-LCS / PEX 24-002
- Keywords
- Lung Cancer, Lung Nodule, Tobacco, Lung Cancer Screening
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 7 participants (estimated)
- Lead sponsor
- VA Office of Research and DevelopmentUS federal agency
- Collaborators
- VA Oncology and Precision Medicine, VA Tobacco Use Treatment National Program Office, VA National Center for Lung Cancer Screening
- Study start
- 1 Oct 2026 (estimated)
- Primary completion
- 30 Jun 2027 (estimated)
- Study completion
- 30 Jun 2027 (estimated)
- First posted
- 20 Dec 2024 (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.
Lung cancer is the leading cause of cancer-related death among Veterans with 90% of cases attributable to smoking. Lung cancer screening (LCS) combined with smoking cessation saves the most lives. ICARE-LCS seeks to decrease health inequality and improve Veteran health by reducing smoking rates among Veterans receiving LCS. ICARE-LCS will use implementation methods to inform national cancer prevention efforts and build infrastructure necessary to support broad implementation of high-impact tobacco dependence treatment (TDT) processes in LCS programs.
Detailed description
The primary goal is to improve the delivery of tobacco dependence treatment (TDT) within Veterans Affairs (VA) lung cancer screening (LCS) programs. LCS with annual low-dose computed tomography saves lives through the early detection of lung cancer and is being broadly deployed, now at 113 VA medical centers. Due to the eligibility criteria selecting for current or previous smoking, 50-60% of LCS participants currently smoke. Modeling studies support that integrating TDT into LCS nearly doubles the benefit of the screening itself. Therefore, access to high-quality TDT is a program requirement per the VA LCS guidance memo.
Though a robust integration of LCS and TDT is a VA priority, in reality there remains a gap in both reach and intensity of TDT for LCS participants. Guidelines and evidence support TDT processes that include 1) systematic assessment and connection to treatment (e.g. Ask-Advise-Connect, motivational interviewing, optout or proactive strategies) and 2) treatment that includes the evidence-based combination of intensive pharmacologic and behavioral treatments ('combined TDT'). Recent trials in LCS participants found high rates of agreeing to treatment using 'opt-out' motivational referral strategies and the highest cessation rates using a longitudinal "chronic disease" model that delivers combined TDT over a period up to a year. Unfortunately, relatively few Veterans in LCS receive any TDT and the treatment is usually inconsistent with guidelines and this evidence. In a national sample of LCS participants who smoke, only 16.4% received any pharmacotherapy for TDT, many under-dosed with short-acting nicotine replacement alone, and fewer than 1% received the recommended combination of behavioral and pharmacologic treatment. This represents a significant gap in care. Improving quality of TDT for Veterans in LCS has been identified as a priority area by multiple stakeholders including the Office of Oncology and Precision Medicine (OPM), the investigators' operational partner, the VA Lung Precision Oncology Program (LPOP), the White House Prevention and Screening Task Force, the National Committee for Quality Assurance and Veterans engagement groups. Each care process-LCS and TDT-is complex on its own, which has hampered integration. While some LCS processes are standardized across VA through use of the tools provided by the National Center for Lung Cancer Screening (NCLCS), individual LCS programs use varied care models. Programs can be 'centralized' (most LCS-related care is delivered by dedicated program staff) or 'hybrid,' where responsibilities are shared between primary care and LCS staff. NCLCS has worked with VAs across the country to enhance LCS quality and uptake. Individual LCS programs deliver combined TDT variably, and many processes are not adapted for the longitudinal, annual LCS process. The VA Tobacco Use Treatment Program Office (TUT) is currently conducting a pilot funded by the Cancer Moonshot to demonstrate feasibility of integrating TDT into LCS, recently expanded from 11 to 15 sites. The Minneapolis VA has conducted a VISN 23-Quality Enhancement Research Initiative (QUERI) partnered implementation pilot to understand barriers and needs among diverse LCS programs, identifying many modifiable targets. The VISN 23 QUERI Team and TUT have collaborated to design an LCS-TDT toolkit that will soon be nationally available. While an important step, a toolkit alone may be insufficient to increase uptake of best practices. Tailored implementation support through intensive external facilitation may be necessary to effectively integrate TDT processes within the VA LCS landscape. With support from the operational partner, OPM, this project proposes to work with TUT and the NCLCS to build on existing efforts to increase participation in combined TDT for LCS participants. This project will utilize both retrospective data analysis and prospective data gathering to inform and tailor a toolkit for national dissemination. ICARE-LCS is an implementation evaluation study model.
Specific Aims:
Aim 1: Identify key process components of effective tobacco treatment programs in LCS and success factors for providing combined TDT. A mixed methods assessment will be conducted at 10 sites in the TUT Moonshot pilot, first qualitatively assessing their current TDT-LCS processes, success factors and perceived barriers to implementation of combined TDT. Data will then be linked with quantitative data of treatment participation and short-term cessation. Findings will be used to refine the toolkit for use in Aim 2 and nationally.
Aim 2: Test a multicomponent facilitation package to improve integration of TDT and LCS.
Seven programs will be identified from among LPOP sites outside of the TUT pilot, ensuring variation in site characteristics (e.g. hybrid vs centralized model), and provided implementation support using external facilitation. Sites will be matched at least 1:1 to another site in the LPOP network that will receive implementation as usual (controls). The primary outcome will be penetration (participation in combined TDT, secondary outcome any treatment) with additional secondary outcomes of fidelity (ideal TDT), and effectiveness (short-term cessation).
Aim 3: Evaluate the implementation outcomes of feasibility, acceptability, fidelity, appropriateness, and cost of implementing TDT integrated with LCS, assessed among Veterans and care team members.
Implementation outcomes other than cost will be assessed using qualitative methods. Cost will be examined related to the implementation support and to the TDT provided (e.g. LCS staff costs, pharmacotherapy, tobacco-related visits) using staff logs and VA pharmacy and billing data. Collectively, the above program evaluation will inform national cancer prevention efforts and build infrastructure necessary to support broad implementation of high-impact TDT processes in LCS programs.
Study design
- Observational model
- Other
- Time perspective
- Other
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Veterans Participating in Lung Cancer Screening who Smoke | – | –Veterans participating in lung cancer screening who smoke and are receiving care at participating VA medical centers |
| Participating VA Medical Centers | – | Other: External FacilitationSeven sites that have agreed to participate in implementation intervention |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Participating VA Medical Centers
Key inclusion criteria (1 listed)
- This is a VAMC based Quality Improvement Partnered Evaluation Initiative. VA sites from around the country that agreed to participate are included.
Key exclusion criteria (1 listed)
- N/A
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 |
|---|---|---|
| External FacilitationMulti-component facilitation strategy to address identified implementation needs | Other | Participating VA Medical Centers |
Primary outcome
Receipt of Combined Tobacco Dependence Treatment
Time frame: Approximately 3 years
Participation in counseling and pharmacotherapy within 90 days of lung cancer screening referral
5 secondary outcomes
Number of Veterans Receiving ANY Tobacco Dependence Treatment Therapy
Time frame: Approximately 3 years
Number of Veterans Receiving of Pharmacotherapy or Counseling Alone
Time frame: Approximately 3 years
Cost Associated with Tobacco Dependence Treatment Among Lung Cancer Screening Participants who Smoke
Time frame: Approximately 3 years
Rate of Short-term Cessation Among Veterans In Lung Cancer Screening who Smoke
Time frame: Approximately 3 years
Implementation Outcomes Assessed at Participating Sites
Time frame: Approximately 3 years
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 26 May 2026.
- Individual participant dataSharing planned: No
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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.
Anne C. Melzer, MD MS principal investigator
Minneapolis VA Health Care System, Minneapolis, MN
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Tobacco Dependence Treatment and Lung Cancer Screening, run by VA Office of Research and Development at 1 site in United States.
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 1 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 26 May 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 United States. 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 Anne C Melzer, MD MS ((612) 725-2000 ext. 4400, Anne.Melzer2@va.gov), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Receipt of Combined Tobacco Dependence Treatment (time frame: Approximately 3 years). 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 26 May 2026.