Smoking Cessation Intervention for Cancer Patients

NAActive, not recruitingINTERVENTIONAL
Enrollment

204

Participants

Timeline

Start Date

October 22, 2002

Primary Completion Date

September 18, 2026

Study Completion Date

September 18, 2026

Conditions
Newly Diagnosed Cancer Patients
Interventions
BEHAVIORAL

Hospital Counseling + Nicotine Replacement Therapy. questionaires

"brief face-to-face or telephone tobacco cessation counseling provided by a tobacco cessation specialist prior to admission and during hospitalization (15-20 minutes per encounter)provision of multi-media self-help materials (e.g., Smoking Cessation Guide for Cancer Patients and Their Families) tailored to address cancer-specific issues such as the benefits and barriers of quitting for cancer patients; 3) tobacco cessation pharmacotherapy, unless medically contraindicated (for this study we will standardize the pharmacotherapy as transdermal nicotine patch), and; 4) two brief telephone counseling (15 minutes) sessions completed as seen clinically appropriate by the tobacco cessation specialists. The content of these counseling sessions is based on the patient's smoking status."

BEHAVIORAL

Hospital Counseling + Nicotine Replacement + Presurgical Scheduled Reduced Smoking, questionaires

Same components of HC+NRT as well as the PS/SRS enhancement.The research team will provide education about scheduled reduced smoking either in person or over the phone. Purpose of the training session, will be audio taped, to prepare participants for daily PDA use over the dur of the scheduled-reduced smoking intervention. Training will demonstrate use of PDA and simulate common technical and procedural issues that might arise during the intervention (e.g., forgetting to record a cigarette or wake time; repeating a day's schedule if needed, prior to the quit date). The simulation will reflect anticipated problems and those identified by users of the PDA. A study helpline number and instructional manual will be provided. A member of the research staff will contact the study participants, once the reduced smoking schedule has begun, to check that the patient understands the schedule and that the PDA is working properly. Estimate patient training with the PDA will require 30 minutes.

Trial Locations (1)

10065

Memorial Sloan Kettering Cancer Center, New York

All Listed Sponsors
collaborator

M.D. Anderson Cancer Center

OTHER

lead

Memorial Sloan Kettering Cancer Center

OTHER