Relapse-prevention counseling added to standard care for cancer patients who quit smoking at diagnosis
Official title: Effectiveness of a Cognitive Behavioral Therapy-Based Smoking Relapse Prevention Intervention Among Patients With Cancer at a Hospital in Vietnam
Run by Vietnam National Cancer Hospital · NCT07815912 · Data updated 2026-11-12
This trial tests whether adding one structured CBT-based relapse-prevention session helps cancer patients who have remained smoke-free since diagnosis stay abstinent longer.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 498 (estimated) |
| Sponsor | Vietnam National Cancer Hospital Indiv |
| Locations | 1 site (Hà Nội) |
| Status | Recruiting |
| Started | October 20, 2026 |
| Main results expected | July 15, 2027 |
| Study ends | July 17, 2027 |
| Registry record updated | October 21, 2026 |
| Trial ID | NCT07815912 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (18+) with cancer who smoked cigarettes at diagnosis and have remained completely abstinent from smoking since diagnosis until enrollment.
✕Probably not a fit
Participants who relapse or never smoke again after enrollment may not derive additional benefit from the CBT session.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized, two-arm, parallel-group trial compares standard brief relapse-prevention counseling to standard counseling plus one additional structured CBT-based relapse-prevention session in adults with cancer who have remained completely abstinent from smoking since their diagnosis. All participants first receive a brief 3-5 minute counseling session, then are randomized to either receive no extra CBT or one 20-30 minute CBT session. Participants are followed for 3 months after randomization at the Vietnam National Cancer Hospital in Hanoi, using intention-to-treat analysis. The study aims to determine if the added CBT session improves sustained smoking abstinence compared with standard counseling alone.
Why it matters
Potential benefit: If successful, patients may have a higher chance of maintaining long-term tobacco abstinence, which could support better cancer-related outcomes.
How similar studies have gone: Prior relapse-prevention approaches in oncology have shown mixed results; this study tests a targeted one-session CBT addition in a specific abstinent-at-enrollment population.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Aged 18 years or older. 2. Diagnosed with cancer. 3. Was smoking combustible cigarettes at the time of cancer diagnosis. 4. Has remained completely abstinent from cigarette smoking from the time of cancer diagnosis until study enrollment, without smoking even a puff. 5. Provides written informed consent to participate in the study. Exclusion Criteria: 1. Have a medical, psychiatric, cognitive, hearing, speech, or other condition that prevents effective communication or meaningful participation in the counseling intervention or study assessments. 2. Are not expected to be contactable or able to complete the planned follow-up assessments. 3. Are currently using other combustible tobacco products, such as waterpipe tobacco, shisha/hookah, cigars, or pipes. 4. Are currently participating in another structured smoking-cessation intervention or clinical trial that could materially affect the study outcomes.
Where it's running
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Vietnam National Cancer Hospital
Hà Nội, Vietnam Recruiting
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.