Brief Smoking Intervention for Women Undergoing Breast Cancer Surgery

Herlev Hospital

Status: Completed

Conditions: Breast Cancer; Smoking

Treatments: Behavioral: Brief preoperative smoking intervention

Study type: Interventional

Funder types: Other

Identifiers

NCT00299117

KA-20060007

Details and patient eligibility

About

The primary purpose of this study is to examine the effect of a brief preoperative smoking intervention on postoperative complications in women undergoing breast cancer surgery.

Secondary purposes are to examine long-term smoking cessation rates and experienced stress and nicotine withdrawal symptoms during the smoking cessation period.

Full description

Smokers are at greater risk of developing postoperative complications. The connection between smoking and cardiovascular and pulmonary disease is furthermore well documented.

Smoking cessation 6 weeks before orthopaedic surgery significantly reduces the risk of developing postoperative complications. However, smoking cessation for an even shorter period may theoretically have similar effects on postoperative complications.

Intensive smoking intervention programmes increase long-term smoking cessation rates significantly. Little evidence is available on the efficacy of brief smoking intervention programmes for newly diagnosed cancer patients.

This study therefore aims to examine the effect of a brief smoking intervention on postoperative complications and long-term smoking cessation rates in women undergoing breast cancer surgery.

The study is a randomised clinical trial in which study participants are randomised by block randomisation to either standard care (control group) or a brief preoperative smoking intervention (intervention group). Patients in the intervention group are counselled to comply with an intended perioperative smoking cessation period of 13 days.

The intervention and control groups will be compared up to 12 months postoperatively in regard to frequency of postoperative complications and smoking cessation rates. Additionally, experienced stress and nicotine withdrawal symptoms during the perioperative smoking cessation period will be compared between the groups.

Enrollment: 130 patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Woman
• Scheduled for elective breast cancer surgery
• Daily smoker
• Age 18 years and above
• Able to read and write Danish
• Informed consent.

Exclusion criteria

• Alcohol intake >35 units per week
• Diagnosed psychiatric disease (including substance abuse and dementia)
• ASA IV and V
• Preoperative neo-adjuvant chemotherapy
• Ulcerating cancer
• Pregnancy and breast-feeding.

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind