Clinical trial · Interventional
Personalized Intervention Program: Tobacco Treatment for Patients at Risk for Lung Cancer (PIP)
NCT02658032CI-TRIAL-00065842completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The purpose of this study is to test the efficacy of two separate, sequential interventions to promote tobacco cessation/reduction in patients who are screened for lung cancer or are eligible for lung cancer screening. Each intervention will be compared to standard of care. The first intervention will be a personalized message intervention, the second intervention will consist of a biofeedback-based intervention.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Biofeedback | — | UNRESOLVED | — |
| Smoking Cessation | — | UNRESOLVED | — |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| bio feedback | Behavioral | — | UNRESOLVED |
| personalized cessation care | Behavioral | — | UNRESOLVED |
| standard care | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (4)
- type
- OTHER
- label
- Standard Care/No Bio Feedback
- description
- This arm will consist of those first randomized to be enrolled in the standard care arm and then those enrolled in the non bio feedback arm.
- interventionNames
- Other: standard care
- type
- OTHER
- label
- Standard Care/ Bio Feedback
- description
- This arm will consist of those first randomized to be enrolled in the standard care arm and then those enrolled in the bio feedback arm.
- interventionNames
- Behavioral: bio feedback
- Other: standard care
- type
- OTHER
- label
- Personalized Care/ No Bio Feedback
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 50 Years
Show eligibility criteria text
Inclusion Criteria: * Current Smoker. * 20 pack per year smoking history. * Eligible for the Smilow treatment program. * Willing to enroll in smoking cessation program. * Willing to be randomized in smoking cessation study. * English speaking. Exclusion Criteria: * Dementia or current serious psychiatric or unstable medical illness. * Pregnancy or breast feeding. * Known fat malabsorption diseases that may affect skin carotenoid status.
References
Publications (1)
- DERIVEDCartmel B, Fucito LM, Bold KW, Neveu S, Li F, Rojewski AM, Gueorguieva R, O'Malley SS, Herbst RS, Toll BA. Effect of a Personalized Tobacco Treatment Intervention on Smoking Abstinence in Individuals Eligible for Lung Cancer Screening. J Thorac Oncol. 2024 Apr;19(4):643-649. doi: 10.1016/j.jtho.2023.11.012. Epub 2023 Nov 15. PMID 37977486