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Preoperative Nicotine Cessation for Women With Breast Cancer Recommended for Reconstruction

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clinicaltrials.gov/study/NCT06461650
Is a
‌
Clinical study
0

Clinical Study attributes

NCT Number
NCT064616500
Health Conditions in Trial
‌
Breast Cancer
0
Trial Recruitment Size
200
Trial Sponsor
University of Florida
University of Florida
0
Clinical Trial Start Date
2024
0
Primary Completion Date
2028
0
Study Completion Date
2029
0
Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Treatment0
Intervention Type
Behavioral0
Interventional Trial Phase
Not Applicable0
Official Name
Preoperative Nicotine Cessation for Women With Breast Cancer Recommended for Reconstruction0
Last Updated
June 17, 2024
0
Allocation Type
NA0
Intervention Model
Single Group Assignment0
Masking Type
None (Open Label)0

Other attributes

Intervention Treatment
Nicotine cessation program0
Study summary

Close to 20% of cancer patients currently use nicotine products. Nicotine use in breast cancer patients is associated with poorer overall outcomes, including worsened survival and increased surgical complications. Nicotine cessation is rarely addressed in breast cancer patients at the time of diagnosis and may be a missed opportunity to optimize patient outcomes. Patients that use nicotine products are not offered reconstruction at time of mastectomy or oncoplastics at the time of lumpectomy, which can be emotionally distressing in women with breast cancer. Reconstruction could be an additional motivating factor in nicotine cessation success. This study aims to evaluate the feasibility of a nicotine cessation program designed by Area Health Education Center (AHEC) in the target population. The study is designed to test the acceptability, and preliminary efficacy of a formal nicotine cessation program in women actively using nicotine products with breast cancer recommended for reconstructive or oncoplastics surgery.

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