New study tests better smoking cessation plans for cancer patients
NCT ID NCT06218823
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested two different smoking cessation treatments in 52 adult cancer patients who had been diagnosed within the past 3 years. One group received a 12-week course of the medication varenicline plus 7 counseling calls tailored to cancer patients. The other group received a standard approach: 2 weeks of nicotine patches plus 3 brief counseling calls. The main goal was to see which treatment helped more patients stay smoke-free 26 weeks after their quit date.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- varenicline and nicotine patch
- What this could lead to
- If successful, this could identify a more effective way to help cancer patients quit smoking, improving their overall health and treatment outcomes.
- What could go wrong
- This is a small pilot study with only 52 participants, so results may not apply to all cancer patients. The treatments may not show a clear difference in effectiveness.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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52 people
The number who actually took part.
- Started
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Mar 2024
- Finished
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Aug 2025
- 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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18 years and older
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Alive (per medical record) * Diagnosed with cancer in the past 3 years * Received care from a participating oncology clinic in the past year * Has a current tobacco use status * Does not have a preferred language other than English (missing language preference will be included). * Valid address that is not a correctional facility or residential treatment/care facility. * No flag for patient cognitive impairment, activated health care power of attorney, or other health care agent (e.g., legally authorized representative) in the EHR. The following additional inclusion criteria must be met for inclusion in the CET * Smoked combustible cigarettes in the past month. * Able to speak and understand English. * Willing to set a date to quit smoking in the next 60 days. * Willing to receive smoking treatment information. * Willing to complete study activities. Exclusion Criteria: * No current suicidal ideation. * Suicide attempt in the past year. * Currently receiving treatment for bipolar disorder, schizophrenia, schizoaffective disorder, or psychotic disorder. * Incarceration. * Unable to provide informed consent to treatment (i.e., cannot answer questions about study procedures or risks after hearing about the study).
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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.
Contacts and locations
Locations
-
UW Carbone Cancer Center
Madison, Wisconsin, 53792, United States
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