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Peri Operative Smoking Cessation Program

Development and Implementation of a Peri Operative Smoking Cessation Program With Computer Based Patient Education.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02053155
Enrollment
345
Registered
2014-02-03
Start date
2013-07-31
Completion date
2015-06-30
Last updated
2015-12-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Smoking Cessation

Keywords

Smoking cessation, perioperative complication, Smokerlyzer, smokers help line

Brief summary

Implementation of a perioperative smoking cessation program with computer based patient education increases the rate of short term (1 month) and long term (6 month) reduces the incidence of perioperative complications in elective surgical patients.

Detailed description

Patients will be enrolled in the quit smoking before surgery program. Before participating in the education program, the investigators will ask patients questions about their smoking habits, and patient will complete pre-education questionnaires that should take about 5 minutes. Patients will participate in a computer-based education program about quitting smoking for about 15 minutes. It will explain the importance of quitting smoking before their surgery, how to quit and coping with quitting. If they are not familiar with using a computer, we will provide an assistant for them to complete the education program. After completing the education program, they will complete a post-education questionnaire. patients will also receive an information pamphlet. All participants will receive the computer-based education program, brief counselling, pamphlet, Smokers' Helpline referral, and telephone follow-up. Altogether you will be spending about 30 minutes to complete the assessment, education program and counselling. patients will be asked for their permission to inform their family physician about their participation in this study. Their smoking status, date of surgery, quit date, and recommended medication (when appropriate) will be faxed to your family physician to assist them quitting process. If they are willing to accept the assistance from Smokers' Helpline, their name and phone number will be faxed to the Smokers' Helpline, and someone from Smokers' Helpline will call you in the next 48 hours to follow-up. The investigators will monitor patient's smoking behavior by measuring expired carbon monoxide, a gas in the air they breathe out, during their pre-surgery visit and on the day of surgery. We also will measure urine cotinine (a by-product of nicotine) by taking urine samples and check their smoking status by asking questions about their smoking habits on the day of surgery, 1 month, 3 months and 6 months after their surgery. During the telephone interview follow-up, we will remind them to do the urine cotinine and mail it to us. (Prepaid mail with urine cotinine strip will be provided at the time of the 2nd visit on the day of surgery.) Each follow-up phone call will take about 6 -10 minutes. A one-month,3 month and 6 month follow up will be done by the research coordinator to assess the smoking status. Brief counseling (\< 5 mins) will be provided.

Interventions

BEHAVIORALComputer based patient education

Sponsors

University Health Network, Toronto
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients\> 18 years of age * self reported smokers ( daily or non daily smokers) * Scheduled for elective surgical procedures

Exclusion criteria

* patients who cannot read and understand English * Have any form of cognitive impairment * Do not have a telephone * Drug or alcohol abuser dependence within the past year * Patients whop are already on pharmacotherapy for smoking cessation.

Design outcomes

Primary

MeasureTime frameDescription
Quit rate6 monthwe will do urine cotinine analysis to confirm the abstinence

Secondary

MeasureTime frameDescription
Surgical outcome1 monthwe will do a chart review to find out the intraoperative and post operative complications

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026